Variant report

Variant	nsv543642
Chromosome Location	chr18:9133164-9191739
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1498)
CpG islands
(count:671)
Chromatin interactive
region (count:78)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:9135696-9136039	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:9190871-9190976	K562	blood:	n/a	n/a
3	ARID3A	chr18:9136447-9136673	K562	blood:	n/a	n/a
4	ARID3A	chr18:9147804-9148215	K562	blood:	n/a	n/a
5	ARID3A	chr18:9136404-9136757	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:9191539-9191994	K562	blood:	n/a	n/a
7	ARID3A	chr18:9135808-9136013	K562	blood:	n/a	n/a
8	ATF1	chr18:9135779-9136091	K562	blood:	n/a	n/a
9	ATF1	chr18:9157891-9157988	K562	blood:	n/a	n/a
10	ATF2	chr18:9135793-9136174	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr18:9143649-9144293	GM12878	blood:	n/a	n/a
12	ATF2	chr18:9143629-9144274	GM12878	blood:	n/a	n/a
13	ATF2	chr18:9135590-9137096	GM12878	blood:	n/a	n/a
14	ATF2	chr18:9136107-9136415	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr18:9136600-9136893	GM12878	blood:	n/a	n/a
16	ATF3	chr18:9136551-9137010	K562	blood:	n/a	n/a
17	ATF3	chr18:9136478-9136960	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr18:9136553-9136994	HepG2	liver:	n/a	n/a
19	ATF3	chr18:9136505-9136965	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr18:9136442-9136940	K562	blood:	n/a	chr18:9136459-9136479
21	ATF3	chr18:9136563-9136937	HepG2	liver:	n/a	n/a
22	ATF3	chr18:9136476-9137007	GM12878	blood:	n/a	n/a
23	BACH1	chr18:9190533-9190568	K562	blood:	n/a	n/a
24	BACH1	chr18:9136277-9136688	K562	blood:	n/a	n/a
25	BACH1	chr18:9135875-9136745	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr18:9173638-9174013	GM12878	blood:	n/a	chr18:9173845-9173856
27	BATF	chr18:9143746-9143985	GM12878	blood:	n/a	n/a
28	BATF	chr18:9140446-9140652	GM12878	blood:	n/a	n/a
29	BATF	chr18:9143650-9144001	GM12878	blood:	n/a	n/a
30	BCL11A	chr18:9143651-9143954	GM12878	blood:	n/a	n/a
31	BCL3	chr18:9135488-9137165	K562	blood:	n/a	chr18:9136241-9136254 chr18:9136609-9136618 chr18:9136188-9136201 chr18:9136184-9136197
32	BCL3	chr18:9135770-9137110	GM12878	blood:	n/a	chr18:9136241-9136254 chr18:9136609-9136618 chr18:9136188-9136201 chr18:9136184-9136197
33	BCLAF1	chr18:9143651-9144074	GM12878	blood:	n/a	n/a
34	BCLAF1	chr18:9143550-9144052	GM12878	blood:	n/a	n/a
35	BCLAF1	chr18:9135756-9137092	GM12878	blood:	n/a	chr18:9136241-9136254 chr18:9136609-9136618 chr18:9136188-9136201 chr18:9136184-9136197
36	BCLAF1	chr18:9139675-9140162	GM12878	blood:	n/a	n/a
37	BCLAF1	chr18:9147804-9148364	GM12878	blood:	n/a	n/a
38	BCLAF1	chr18:9135689-9137178	GM12878	blood:	n/a	chr18:9136241-9136254 chr18:9136609-9136618 chr18:9136188-9136201 chr18:9136184-9136197
39	BCLAF1	chr18:9137319-9138210	GM12878	blood:	n/a	chr18:9137453-9137466
40	BCLAF1	chr18:9137310-9138220	GM12878	blood:	n/a	chr18:9137453-9137466
41	BHLHE40	chr18:9147785-9148276	GM12878	blood:	n/a	n/a
42	BHLHE40	chr18:9135799-9137881	HepG2	liver:	n/a	chr18:9137523-9137539 chr18:9137515-9137531 chr18:9136608-9136624 chr18:9137555-9137571
43	BHLHE40	chr18:9136580-9136904	HepG2	liver:	n/a	chr18:9136608-9136624
44	BHLHE40	chr18:9135800-9138071	K562	blood:	n/a	chr18:9137523-9137539 chr18:9137515-9137531 chr18:9136608-9136624 chr18:9137555-9137571
45	BHLHE40	chr18:9140386-9140680	GM12878	blood:	n/a	n/a
46	BHLHE40	chr18:9135643-9138175	GM12878	blood:	n/a	chr18:9137523-9137539 chr18:9137515-9137531 chr18:9136608-9136624 chr18:9137555-9137571
47	BHLHE40	chr18:9136537-9136955	HepG2	liver:	n/a	chr18:9136608-9136624
48	BHLHE40	chr18:9136432-9136926	A549	lung:	n/a	chr18:9136608-9136624
49	BRCA1	chr18:9136870-9136896	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr18:9135801-9136902	Hela-S3	cervix:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:9141063-9141113	NH-A	brain:	n/a
2	chr18:9136603-9136653	ovcar-3	ovarian:	n/a
3	chr18:9136598-9136648	HUVEC	blood vessel:	n/a
4	chr18:9135843-9135893	SK-N-SH_RA	brain:	n/a
5	chr18:9141063-9141113	HCM	heart:	n/a
6	chr18:9137949-9137999	GM12878	blood:	n/a
7	chr18:9136598-9136648	HRPEpiC	eye:	n/a
8	chr18:9137949-9137999	HEEpiC	esophagus:	n/a
9	chr18:9137949-9137999	HL-60	blood:	n/a
10	chr18:9136603-9136653	GM12878	blood:	n/a
11	chr18:9137949-9137999	GM12892	blood:	n/a
12	chr18:9137021-9137071	GM12878	blood:	n/a
13	chr18:9137021-9137071	NHDF-neo	bronchial:	n/a
14	chr18:9136381-9136431	ovcar-3	ovarian:	n/a
15	chr18:9136852-9136902	LNCaP	prostate:	n/a
16	chr18:9136852-9136902	NB4	blood:	n/a
17	chr18:9136565-9136615	A549	lung:	n/a
18	chr18:9135843-9135893	AG09319	gingival:	n/a
19	chr18:9137021-9137071	HEEpiC	esophagus:	n/a
20	chr18:9137949-9137999	Caco-2	colon:	n/a
21	chr18:9136381-9136431	BE2_C	brain:	n/a
22	chr18:9141063-9141113	NHDF-neo	bronchial:	n/a
23	chr18:9136381-9136431	HAEpiC	amniotic membrane:	n/a
24	chr18:9136711-9136761	H1-hESC	embryonic stem cell:	embryo
25	chr18:9135843-9135893	NH-A	brain:	n/a
26	chr18:9136565-9136615	H1-hESC	embryonic stem cell:	embryo
27	chr18:9137949-9137999	Jurkat	blood:	n/a
28	chr18:9137021-9137071	BE2_C	brain:	n/a
29	chr18:9141063-9141113	GM12878	blood:	n/a
30	chr18:9136598-9136648	A549	lung:	n/a
31	chr18:9136381-9136431	NH-A	brain:	n/a
32	chr18:9136852-9136902	HPAEpiC	pulmonary alveolar:	n/a
33	chr18:9137021-9137071	LNCaP	prostate:	n/a
34	chr18:9137021-9137071	ovcar-3	ovarian:	n/a
35	chr18:9136852-9136902	K562	blood:	n/a
36	chr18:9136598-9136648	HEK293	kidney:	embryo
37	chr18:9136711-9136761	PrEC	prostate:	n/a
38	chr18:9137021-9137071	HRE	kidney:	n/a
39	chr18:9137949-9137999	HEK293	kidney:	embryo
40	chr18:9136598-9136648	PFSK-1	brain:	n/a
41	chr18:9137021-9137071	BJ	skin:	n/a
42	chr18:9136556-9136606	HRCEpiC	kidney:	n/a
43	chr18:9136381-9136431	A549	lung:	n/a
44	chr18:9141063-9141113	PFSK-1	brain:	n/a
45	chr18:9136711-9136761	SK-N-SH_RA	brain:	n/a
46	chr18:9136603-9136653	HCPEpiC	choroid plexus:	n/a
47	chr18:9137949-9137999	AG10803	skin:	n/a
48	chr18:9137021-9137071	HCM	heart:	n/a
49	chr18:9135843-9135893	HRE	kidney:	n/a
50	chr18:9136603-9136653	AG09309	skin:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:9102185..9104262-chr18:9139524..9141518,2	MCF-7	breast:
2	chr16:69788330..69789298-chr18:9136242..9137229,2	Hela-S3	cervix:
3	chr18:9137564..9140546-chr18:9188464..9190895,2	MCF-7	breast:
4	chr18:9012557..9014644-chr18:9143805..9146448,2	K562	blood:
5	chr18:9143953..9145593-chr18:9149699..9152459,2	MCF-7	breast:
6	chr18:9150679..9153194-chr18:9154073..9157031,2	K562	blood:
7	chr18:9137627..9140441-chr18:9161165..9162837,2	K562	blood:
8	chr18:9181280..9182964-chr18:9185085..9186972,2	K562	blood:
9	chr18:9103321..9105188-chr18:9146255..9148177,2	MCF-7	breast:
10	chr18:9150679..9153194-chr18:9154073..9157031,2	K562	blood:
11	chr1:149857838..149858809-chr18:9136877..9137598,2	Hela-S3	cervix:
12	chr18:9142397..9144914-chr18:9146594..9148410,2	K562	blood:
13	chr18:9137564..9140546-chr18:9188464..9190895,2	MCF-7	breast:
14	chr18:9138656..9141235-chr18:9149570..9151773,2	MCF-7	breast:
15	chr18:9191112..9193775-chr18:9197771..9201381,3	K562	blood:
16	chr18:8608734..8611272-chr18:9134054..9137046,2	K562	blood:
17	chr18:9136798..9138761-chr18:9150520..9152733,3	K562	blood:
18	chr18:9123369..9127442-chr18:9129820..9133797,5	MCF-7	breast:
19	chr18:9186304..9188662-chr18:9189391..9191819,2	K562	blood:
20	chr18:9143953..9145593-chr18:9149699..9152459,2	MCF-7	breast:
21	chr18:9175098..9178757-chr18:9180431..9183034,3	K562	blood:
22	chr18:9117343..9120126-chr18:9132921..9134783,2	K562	blood:
23	chr18:8704166..8706937-chr18:9136436..9139051,3	MCF-7	breast:
24	chr18:9115829..9117482-chr18:9134395..9136348,2	MCF-7	breast:
25	chr18:9073419..9074239-chr18:9147700..9148986,7	MCF-7	breast:
26	chr18:9073278..9074237-chr18:9147638..9148595,6	K562	blood:
27	chr18:9135921..9136800-chr19:1241349..1242081,2	Hela-S3	cervix:
28	chr18:9177075..9179067-chr18:9181095..9183827,3	K562	blood:
29	chr18:9145780..9149293-chr18:9151722..9154723,3	MCF-7	breast:
30	chr18:9116916..9118754-chr18:9136071..9139010,3	K562	blood:
31	chr1:147806600..147807177-chr18:9136691..9137307,2	Hela-S3	cervix:
32	chr18:9142397..9144914-chr18:9146594..9148410,2	K562	blood:
33	chr18:9182719..9184745-chr18:9190563..9192792,3	K562	blood:
34	chr18:9189637..9191991-chr18:9193161..9195966,2	K562	blood:
35	chr18:9114265..9115952-chr18:9154606..9156860,2	K562	blood:
36	chr1:166808283..166808793-chr18:9137108..9137608,2	Hela-S3	cervix:
37	chr18:9072068..9073744-chr18:9148593..9150663,2	MCF-7	breast:
38	chr18:9139649..9142253-chr18:9181980..9184460,2	K562	blood:
39	chr18:9142518..9147121-chr18:9149107..9151760,6	K562	blood:
40	chr18:9117343..9119164-chr18:9132921..9135865,2	K562	blood:
41	chr18:9137052..9139682-chr18:9153888..9155527,2	MCF-7	breast:
42	chr18:9100897..9104416-chr18:9134561..9139326,10	MCF-7	breast:
43	chr18:9101542..9104099-chr18:9143850..9147103,3	K562	blood:
44	chr18:9143163..9146307-chr18:9148846..9151084,3	K562	blood:
45	chr18:9146619..9148558-chr18:9153184..9154759,2	K562	blood:
46	chr18:9135268..9138206-chr18:9174153..9176625,2	K562	blood:
47	chr18:9017215..9020121-chr18:9143322..9145391,2	K562	blood:
48	chr18:9113884..9116180-chr18:9136154..9138641,4	K562	blood:
49	chr18:9182300..9184607-chr18:9187847..9189925,2	K562	blood:
50	chr18:9137078..9139236-chr18:9332503..9334760,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP4R1-4	chr18:9133389-9133420	ENSG00000266053.1
2	lnc-PPP4R1-4	chr18:9135711-9136489	ENSG00000266053.2

No data

Variant related genes	Relation type
ENSG00000266053	TF binding region
ANKRD12	TF binding region
ENSG00000266053	CpG island
ANKRD12	CpG island
ENSG00000178127	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000266053	chromatin interactions
ENSG00000141101	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000101745	chromatin interactions
ENSG00000263847	chromatin interactions
ENSG00000206418	chromatin interactions
ENSG00000099624	chromatin interactions
ENSG00000168502	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000264964	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000143157	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000265257	chromatin interactions
ENSG00000242058	chromatin interactions

Extended variants
information (count: 2513 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2513 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375795734	chr18:9133180-9133181	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs72935233	chr18:9133183-9133184	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192916837	chr18:9133269-9133270	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs368640021	chr18:9133369-9133370	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs528487506	chr18:9133384-9133385	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184631842	chr18:9133400-9133401	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs562069134	chr18:9133437-9133438	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs529563769	chr18:9133446-9133447	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs373763079	chr18:9133456-9133457	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs188488242	chr18:9133491-9133492	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs180951450	chr18:9133500-9133501	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs539673659	chr18:9133501-9133502	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs185067361	chr18:9133511-9133512	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs367976167	chr18:9133554-9133555	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs548629545	chr18:9133577-9133578	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs145222314	chr18:9133628-9133629	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs534420607	chr18:9133634-9133635	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs552503467	chr18:9133643-9133644	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs564860221	chr18:9133662-9133663	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs535705056	chr18:9133711-9133712	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs535752510	chr18:9133720-9133721	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs148775623	chr18:9133739-9133740	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs575371184	chr18:9133783-9133784	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545722980	chr18:9133785-9133786	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537407573	chr18:9133798-9133799	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs367555756	chr18:9133815-9133816	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs57462781	chr18:9133845-9133846	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs556948012	chr18:9133883-9133884	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs564284658	chr18:9133895-9133896	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372188518	chr18:9133896-9133897	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs116876812	chr18:9133923-9133924	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs145438134	chr18:9133944-9133945	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540753180	chr18:9133983-9133984	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369968370	chr18:9133988-9133989	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374266092	chr18:9133989-9133990	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562029489	chr18:9134004-9134005	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs189486118	chr18:9134019-9134020	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143762114	chr18:9134046-9134047	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs146888086	chr18:9134071-9134072	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs533562125	chr18:9134073-9134074	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs551518578	chr18:9134138-9134139	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs201073561	chr18:9134150-9134151	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375917534	chr18:9134162-9134163	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs376984569	chr18:9134176-9134177	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs368914351	chr18:9134186-9134187	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs534384070	chr18:9134221-9134222	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs546302509	chr18:9134222-9134223	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs148032289	chr18:9134263-9134264	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs368784815	chr18:9134274-9134275	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs200122696	chr18:9134323-9134324	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2461 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9107000-9135200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr18:9107400-9135400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr18:9107800-9134600	Weak transcription	Fetal Brain Male	brain
4	chr18:9115400-9134600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:9115800-9134800	Strong transcription	Dnd41	blood
6	chr18:9116800-9135200	Strong transcription	Fetal Thymus	thymus
7	chr18:9117200-9134800	Weak transcription	Brain Germinal Matrix	brain
8	chr18:9117400-9135200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr18:9117400-9135600	Weak transcription	Esophagus	oesophagus
10	chr18:9117400-9135800	Weak transcription	Gastric	stomach
11	chr18:9117600-9134800	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr18:9117600-9135200	Weak transcription	Psoas Muscle	Psoas
13	chr18:9117600-9135800	Weak transcription	Pancreas	Pancrea
14	chr18:9117800-9135000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr18:9117800-9135600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr18:9117800-9135800	Weak transcription	Small Intestine	intestine
17	chr18:9118200-9134400	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr18:9118200-9135000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr18:9118400-9134400	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr18:9118600-9134600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr18:9118600-9135000	Strong transcription	H1 Cell Line	embryonic stem cell
22	chr18:9118800-9134400	Strong transcription	K562	blood
23	chr18:9118800-9135600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr18:9118800-9135600	Weak transcription	Right Ventricle	heart
25	chr18:9119200-9134400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr18:9119400-9135200	Weak transcription	Stomach Mucosa	stomach
27	chr18:9119800-9135000	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr18:9119800-9135400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr18:9120000-9134800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr18:9121200-9133200	Strong transcription	Primary hematopoietic stem cells	blood
31	chr18:9121200-9135200	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr18:9121200-9135200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr18:9121400-9134800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr18:9121800-9134800	Strong transcription	Primary B cells from peripheral blood	blood
35	chr18:9122400-9134600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr18:9122800-9134800	Strong transcription	NHDF-Ad	bronchial
37	chr18:9124000-9135600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr18:9125000-9134000	Strong transcription	HSMM	muscle
39	chr18:9125000-9134600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:9125000-9134800	Strong transcription	Placenta	Placenta
41	chr18:9125000-9135000	Strong transcription	GM12878-XiMat	blood
42	chr18:9125200-9134400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
43	chr18:9125200-9135000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr18:9125200-9135600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr18:9125400-9133200	Strong transcription	HepG2	liver
46	chr18:9125400-9134000	Strong transcription	HUVEC	blood vessel
47	chr18:9125400-9134400	Strong transcription	Hela-S3	cervix
48	chr18:9125400-9134600	Strong transcription	Primary B cells from cord blood	blood
49	chr18:9125400-9134800	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr18:9125600-9133800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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