Variant report

Variant	esv1793876
Chromosome Location	chr1:155194112-155212255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1618)
CpG islands
(count:1284)
Chromatin interactive
region (count:135)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1618 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155196578-155196994	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:155211743-155211909	K562	blood:	n/a	n/a
3	ARID3A	chr1:155196486-155197271	K562	blood:	n/a	n/a
4	ARID3A	chr1:155210932-155211354	HepG2	liver:	n/a	n/a
5	ATF1	chr1:155210928-155211236	K562	blood:	n/a	n/a
6	ATF1	chr1:155194483-155194805	K562	blood:	n/a	n/a
7	ATF2	chr1:155210881-155211282	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:155196944-155197904	GM12878	blood:	n/a	n/a
9	ATF2	chr1:155196208-155196851	GM12878	blood:	n/a	n/a
10	ATF2	chr1:155197384-155197948	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:155196936-155197811	GM12878	blood:	n/a	n/a
12	ATF2	chr1:155210887-155211301	GM12878	blood:	n/a	n/a
13	ATF2	chr1:155196290-155196702	GM12878	blood:	n/a	n/a
14	ATF2	chr1:155197384-155197964	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:155210932-155211284	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr1:155211444-155211871	K562	blood:	n/a	n/a
17	ATF3	chr1:155194392-155194847	K562	blood:	n/a	n/a
18	ATF3	chr1:155210895-155211289	H1-hESC	embryonic stem cell:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
19	ATF3	chr1:155210904-155211278	K562	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
20	ATF3	chr1:155210893-155211233	HepG2	liver:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
21	ATF3	chr1:155210878-155211279	A549	lung:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
22	ATF3	chr1:155210797-155211327	HepG2	liver:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
23	ATF3	chr1:155210875-155211296	GM12878	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
24	ATF3	chr1:155210871-155211264	H1-hESC	embryonic stem cell:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
25	ATF3	chr1:155210875-155211383	A549	lung:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
26	ATF3	chr1:155210888-155211238	K562	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
27	ATF3	chr1:155210897-155211162	GM12878	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
28	BACH1	chr1:155196500-155196997	K562	blood:	n/a	n/a
29	BACH1	chr1:155197223-155197305	K562	blood:	n/a	n/a
30	BACH1	chr1:155196510-155197939	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL3	chr1:155196164-155198121	A549	lung:	n/a	n/a
32	BCL3	chr1:155210894-155211423	A549	lung:	n/a	chr1:155211090-155211099
33	BCL3	chr1:155210785-155211265	A549	lung:	n/a	chr1:155211090-155211099
34	BCLAF1	chr1:155196322-155197414	GM12878	blood:	n/a	n/a
35	BDP1	chr1:155196158-155197032	Hela-S3	cervix:	n/a	n/a
36	BDP1	chr1:155193690-155194244	Hela-S3	cervix:	n/a	chr1:155193724-155193737
37	BHLHE40	chr1:155211693-155211793	K562	blood:	n/a	n/a
38	BHLHE40	chr1:155196322-155196799	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:155211008-155211252	GM12878	blood:	n/a	chr1:155211054-155211075
40	BHLHE40	chr1:155196870-155197655	HepG2	liver:	n/a	n/a
41	BHLHE40	chr1:155197067-155197817	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:155196326-155197943	K562	blood:	n/a	n/a
43	BHLHE40	chr1:155194516-155194887	K562	blood:	n/a	n/a
44	BRCA1	chr1:155196161-155198275	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:155211005-155211118	GM12878	blood:	n/a	n/a
46	BRCA1	chr1:155197279-155197444	HepG2	liver:	n/a	n/a
47	BRCA1	chr1:155197194-155197495	GM12878	blood:	n/a	n/a
48	BRCA1	chr1:155210910-155211457	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr1:155196488-155197307	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRF1	chr1:155194594-155195036	Hela-S3	cervix:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155197173-155197223	MCF10A-Er-Src	breast:	n/a
2	chr1:155197502-155197552	SK-N-SH	brain:	n/a
3	chr1:155211079-155211129	H1-hESC	embryonic stem cell:	embryo
4	chr1:155197173-155197223	MCF10A-Er-Src	breast:	n/a
5	chr1:155197502-155197552	SK-N-SH	brain:	n/a
6	chr1:155211079-155211129	H1-hESC	embryonic stem cell:	embryo
7	chr1:155197152-155197202	AG04449	skin:	fetal
8	chr1:155194782-155194832	LNCaP	prostate:	n/a
9	chr1:155194782-155194832	ECC-1	luminal epithelium:	n/a
10	chr1:155197511-155197561	HCM	heart:	n/a
11	chr1:155198391-155198441	GM19239	blood:	n/a
12	chr1:155198391-155198441	A549	lung:	n/a
13	chr1:155197173-155197223	T-47D	breast:	n/a
14	chr1:155197152-155197202	GM12878	blood:	n/a
15	chr1:155197753-155197803	BE2_C	brain:	n/a
16	chr1:155197384-155197434	MCF-7	breast:	n/a
17	chr1:155195300-155195350	GM12891	blood:	n/a
18	chr1:155197564-155197614	SKMC	muscle:	n/a
19	chr1:155197843-155197893	LNCaP	prostate:	n/a
20	chr1:155197384-155197434	HEEpiC	esophagus:	n/a
21	chr1:155197502-155197552	HRE	kidney:	n/a
22	chr1:155198391-155198441	MCF10A-Er-Src	breast:	n/a
23	chr1:155211040-155211090	Hepatocyte	liver:	n/a
24	chr1:155197502-155197552	HEEpiC	esophagus:	n/a
25	chr1:155197502-155197552	GM12878	blood:	n/a
26	chr1:155194782-155194832	AoSMC	blood vessel:	n/a
27	chr1:155197279-155197329	U87	brain:	n/a
28	chr1:155202674-155202724	HCF	heart:	n/a
29	chr1:155198391-155198441	ProgFib	skin:	n/a
30	chr1:155211462-155211512	SK-N-SH_RA	brain:	n/a
31	chr1:155197753-155197803	SAEC	small airway:	n/a
32	chr1:155197152-155197202	HCPEpiC	choroid plexus:	n/a
33	chr1:155211040-155211090	SKMC	muscle:	n/a
34	chr1:155202685-155202735	A549	lung:	n/a
35	chr1:155195300-155195350	SK-N-SH_RA	brain:	n/a
36	chr1:155197692-155197742	HCPEpiC	choroid plexus:	n/a
37	chr1:155197384-155197434	GM12878	blood:	n/a
38	chr1:155197843-155197893	HL-60	blood:	n/a
39	chr1:155211462-155211512	MCF10A-Er-Src	breast:	n/a
40	chr1:155195300-155195350	HRPEpiC	eye:	n/a
41	chr1:155197692-155197742	GM19239	blood:	n/a
42	chr1:155211462-155211512	NH-A	brain:	n/a
43	chr1:155197843-155197893	GM12892	blood:	n/a
44	chr1:155197843-155197893	HRE	kidney:	n/a
45	chr1:155211079-155211129	T-47D	breast:	n/a
46	chr1:155197511-155197561	NH-A	brain:	n/a
47	chr1:155197173-155197223	GM12891	blood:	n/a
48	chr1:155208775-155208825	AG09309	skin:	n/a
49	chr1:155198391-155198441	AG04449	skin:	fetal
50	chr1:155202674-155202724	K562	blood:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
2	chr1:155195599..155199380-chr1:155211353..155216703,7	MCF-7	breast:
3	chr1:155174605..155182734-chr1:155187211..155200915,43	MCF-7	breast:
4	chr1:155200126..155202062-chr1:155213409..155215894,2	MCF-7	breast:
5	chr1:155197037..155198006-chr19:18392015..18392606,2	Hela-S3	cervix:
6	chr1:155195600..155203152-chr1:155209955..155216515,9	MCF-7	breast:
7	chr1:155193544..155197336-chr1:155293049..155296583,5	MCF-7	breast:
8	chr1:155210207..155211789-chr1:155219850..155221900,2	K562	blood:
9	chr1:155196978..155198560-chr1:155209319..155211586,2	K562	blood:
10	chr1:94312249..94313217-chr1:155197097..155198051,2	Hela-S3	cervix:
11	chr1:155196797..155197673-chr7:99698835..99699797,2	Hela-S3	cervix:
12	chr1:155193188..155195403-chr1:155211959..155214156,2	K562	blood:
13	chr1:155176536..155177291-chr1:155196359..155196911,2	MCF-7	breast:
14	chr1:155172877..155174474-chr1:155197003..155199061,2	K562	blood:
15	chr1:155197241..155197754-chr9:130953885..130954667,2	NB4	blood:
16	chr1:155186661..155189522-chr1:155194169..155197986,6	K562	blood:
17	chr1:117602404..117603075-chr1:155196850..155197424,2	Hela-S3	cervix:
18	chr1:155197215..155198001-chr17:7122908..7123728,2	Hela-S3	cervix:
19	chr1:155176324..155177310-chr1:155196150..155197130,9	K562	blood:
20	chr1:155098847..155100942-chr1:155197257..155198807,2	K562	blood:
21	chr1:155148495..155149762-chr1:155196236..155196972,5	MCF-7	breast:
22	chr1:45987235..45987946-chr1:155196847..155197356,2	Hela-S3	cervix:
23	chr1:155188805..155190957-chr1:155195706..155197646,3	K562	blood:
24	chr1:155209487..155212728-chr1:155212760..155217156,9	MCF-7	breast:
25	chr1:155146416..155150261-chr1:155194777..155198198,7	MCF-7	breast:
26	chr1:148241110..148242082-chr1:155197046..155197929,2	Hela-S3	cervix:
27	chr1:155200890..155203810-chr1:155211180..155212788,2	MCF-7	breast:
28	chr1:155149084..155150074-chr1:155196318..155196838,2	MCF-7	breast:
29	chr1:155176293..155177732-chr1:155196164..155197059,7	MCF-7	breast:
30	chr1:155196679..155197559-chr2:20850313..20851127,2	Hela-S3	cervix:
31	chr1:155176431..155180791-chr1:155209413..155214573,7	MCF-7	breast:
32	chr1:155174590..155181850-chr1:155192419..155201858,28	K562	blood:
33	chr1:155196896..155197663-chr2:219264116..219264834,2	Hela-S3	cervix:
34	chr1:155196696..155197276-chr13:99738346..99738910,2	Hela-S3	cervix:
35	chr1:155200890..155203810-chr1:155211180..155212788,2	MCF-7	breast:
36	chr1:155161998..155167332-chr1:155208163..155212538,6	K562	blood:
37	chr1:155191881..155194028-chr1:155195597..155197149,2	MCF-7	breast:
38	chr1:155196728..155197629-chr22:36924753..36925288,2	HCT-116	colon:
39	chr1:155209079..155212795-chr1:155212935..155216540,4	MCF-7	breast:
40	chr1:155193188..155195403-chr1:155211959..155214156,2	K562	blood:
41	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
42	chr1:155196805..155197610-chr9:131486404..131487395,2	Hela-S3	cervix:
43	chr1:155209727..155212678-chr1:155212773..155217086,5	K562	blood:
44	chr1:155195600..155203152-chr1:155209955..155216515,9	MCF-7	breast:
45	chr1:155106515..155109128-chr1:155196131..155198130,2	K562	blood:
46	chr1:155196791..155199483-chr1:155201481..155203519,3	K562	blood:
47	chr1:155194687..155197665-chr1:155223228..155225374,3	MCF-7	breast:
48	chr1:155171519..155180465-chr1:155194608..155199196,19	MCF-7	breast:
49	chr1:155187443..155190276-chr1:155193102..155195669,3	K562	blood:
50	chr1:155211690..155216212-chr1:155231766..155235735,5	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GBA-1	chr1:155201063-155203428	NONHSAT006710

No data

Variant related genes	Relation type
GBA	TF binding region
MTX1P1	TF binding region
ENSG00000216109	TF binding region
GBAP1	TF binding region
GBA	CpG island
MTX1P1	CpG island
ENSG00000216109	CpG island
GBAP1	CpG island
ENSG00000260464	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000147124	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000137203	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000148337	chromatin interactions
ENSG00000236675	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000203667	chromatin interactions
ENSG00000251246	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000089693	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000108506	chromatin interactions
ENSG00000112679	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000197912	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000223478	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000167977	chromatin interactions
ENSG00000139218	chromatin interactions
ENSG00000216109	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000072778	chromatin interactions
ENSG00000118960	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000211575	chromatin interactions
ENSG00000160446	chromatin interactions
ENSG00000229848	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000148341	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000119953	chromatin interactions
ENSG00000160685	chromatin interactions
ENSG00000144579	chromatin interactions
ENSG00000089009	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000088387	chromatin interactions
ENSG00000100353	chromatin interactions
ENSG00000243364	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000137936	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000116830	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000236263	chromatin interactions
ENSG00000255062	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000125967	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000273088	chromatin interactions
ENSG00000132535	chromatin interactions
ENSG00000231064	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000056586	chromatin interactions
ENSG00000271748	chromatin interactions
ENSG00000173933	chromatin interactions

Extended variants
information (count: 831 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:831 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190694360	chr1:155194120-155194121	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs565825708	chr1:155194141-155194142	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs200443581	chr1:155194142-155194143	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs377568346	chr1:155194143-155194144	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs199953803	chr1:155194145-155194146	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs374042798	chr1:155194162-155194163	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs541692734	chr1:155194163-155194164	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs574481049	chr1:155194165-155194166	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs12028078	chr1:155194229-155194230	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs184173871	chr1:155194241-155194242	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs543568743	chr1:155194263-155194264	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs552270247	chr1:155194316-155194317	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs570430755	chr1:155194342-155194343	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs375061186	chr1:155194343-155194344	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs531368657	chr1:155194360-155194361	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs549500280	chr1:155194392-155194393	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs186211273	chr1:155194393-155194394	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs535362477	chr1:155194397-155194398	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs376945748	chr1:155194424-155194425	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
20	rs371117424	chr1:155194427-155194428	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
21	rs565555896	chr1:155194456-155194457	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
22	rs539221862	chr1:155194457-155194458	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs558261894	chr1:155194484-155194485	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs576443897	chr1:155194510-155194511	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
25	rs138751064	chr1:155194615-155194616	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs555476155	chr1:155194633-155194634	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs16836748	chr1:155194679-155194680	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs571929512	chr1:155194786-155194787	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs112227527	chr1:155194861-155194862	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs560058780	chr1:155194872-155194873	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs578231803	chr1:155194906-155194907	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs374166175	chr1:155194975-155194976	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs190676369	chr1:155194976-155194977	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs2049805	chr1:155194980-155194981	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
35	rs531301648	chr1:155194997-155194998	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs6677756	chr1:155195044-155195045	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs139558368	chr1:155195071-155195072	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs374942809	chr1:155195072-155195073	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs59578826	chr1:155195075-155195076	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
40	rs554343302	chr1:155195107-155195108	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs58525188	chr1:155195114-155195115	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs182727399	chr1:155195172-155195173	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs2974931	chr1:155195215-155195216	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs547314459	chr1:155195335-155195336	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs187050017	chr1:155195341-155195342	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs539282884	chr1:155195356-155195357	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs551277911	chr1:155195357-155195358	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs570180800	chr1:155195411-155195412	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs537153842	chr1:155195438-155195439	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs192846542	chr1:155195451-155195452	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1545 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155179600-155195400	Weak transcription	Aorta	Aorta
2	chr1:155179600-155195800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:155179600-155196200	Weak transcription	Pancreas	Pancrea
4	chr1:155179600-155196600	Weak transcription	Gastric	stomach
5	chr1:155179600-155196600	Weak transcription	Small Intestine	intestine
6	chr1:155180000-155195600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:155180600-155195600	Weak transcription	HepG2	liver
8	chr1:155182200-155195800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr1:155182200-155196400	Weak transcription	Esophagus	oesophagus
10	chr1:155182200-155196600	Weak transcription	Lung	lung
11	chr1:155182600-155196200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:155182800-155194800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr1:155182800-155194800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr1:155182800-155196400	Weak transcription	Left Ventricle	heart
15	chr1:155186000-155195200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:155187800-155196000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:155188600-155196600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr1:155189200-155196000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:155189200-155196200	Enhancers	Primary B cells from cord blood	blood
20	chr1:155189400-155195400	Weak transcription	Liver	Liver
21	chr1:155189400-155195400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr1:155189400-155195800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr1:155189400-155196000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:155189400-155196000	Weak transcription	Colon Smooth Muscle	Colon
25	chr1:155189400-155196000	Weak transcription	Fetal Lung	lung
26	chr1:155189400-155196200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr1:155189600-155194400	Weak transcription	HMEC	breast
28	chr1:155189600-155194800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr1:155189600-155195400	Weak transcription	Fetal Brain Male	brain
30	chr1:155189600-155195600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:155189600-155195600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr1:155189600-155195600	Weak transcription	Brain Germinal Matrix	brain
33	chr1:155189600-155196000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr1:155189600-155196200	Weak transcription	Brain Angular Gyrus	brain
35	chr1:155189600-155196200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr1:155189800-155194200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:155189800-155194600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr1:155189800-155194600	Weak transcription	Fetal Kidney	kidney
39	chr1:155189800-155195400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr1:155189800-155195400	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr1:155189800-155195400	Weak transcription	Right Ventricle	heart
42	chr1:155189800-155195400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr1:155189800-155195600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr1:155189800-155195600	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr1:155189800-155195600	Weak transcription	Adipose Nuclei	Adipose
46	chr1:155189800-155195800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr1:155189800-155196200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr1:155189800-155196200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr1:155190000-155194400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr1:155190000-155194600	Weak transcription	Fetal Intestine Small	intestine

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