Variant report

Variant	nsv576495
Chromosome Location	chr18:11917410-11986557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2431)
CpG islands
(count:1220)
Chromatin interactive
region (count:89)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2431 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:11937886-11938254	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:11953120-11953369	K562	blood:	n/a	n/a
3	ARID3A	chr18:11925618-11926210	K562	blood:	n/a	n/a
4	ARID3A	chr18:11946503-11947879	K562	blood:	n/a	n/a
5	ARID3A	chr18:11981509-11981627	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:11951483-11951785	K562	blood:	n/a	n/a
7	ARID3A	chr18:11955409-11955965	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:11981872-11982212	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:11970464-11970725	K562	blood:	n/a	n/a
10	ARID3A	chr18:11982059-11982245	K562	blood:	n/a	n/a
11	ARID3A	chr18:11955577-11955916	K562	blood:	n/a	n/a
12	ARID3A	chr18:11962438-11963239	K562	blood:	n/a	n/a
13	ARID3A	chr18:11948964-11949185	HepG2	liver:	n/a	n/a
14	ARID3A	chr18:11981074-11981228	K562	blood:	n/a	n/a
15	ARID3A	chr18:11954974-11955062	K562	blood:	n/a	n/a
16	ARID3A	chr18:11925142-11925504	HepG2	liver:	n/a	n/a
17	ARID3A	chr18:11980098-11981249	HepG2	liver:	n/a	n/a
18	ARID3A	chr18:11937850-11938277	K562	blood:	n/a	n/a
19	ATF1	chr18:11925758-11926103	K562	blood:	n/a	n/a
20	ATF1	chr18:11953081-11953528	K562	blood:	n/a	n/a
21	ATF1	chr18:11923504-11923703	K562	blood:	n/a	n/a
22	ATF2	chr18:11921705-11922227	GM12878	blood:	n/a	n/a
23	ATF2	chr18:11980997-11981334	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr18:11947108-11947652	GM12878	blood:	n/a	n/a
25	ATF2	chr18:11921722-11922209	GM12878	blood:	n/a	n/a
26	ATF3	chr18:11955691-11955826	HepG2	liver:	n/a	n/a
27	ATF3	chr18:11947132-11947544	A549	lung:	n/a	n/a
28	ATF3	chr18:11955638-11955962	K562	blood:	n/a	n/a
29	ATF3	chr18:11942765-11942979	K562	blood:	n/a	n/a
30	ATF3	chr18:11953195-11953438	K562	blood:	n/a	chr18:11953305-11953316
31	BACH1	chr18:11947183-11947845	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr18:11981477-11981827	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr18:11951676-11951948	K562	blood:	n/a	n/a
34	BACH1	chr18:11955675-11955923	K562	blood:	n/a	n/a
35	BACH1	chr18:11948485-11949070	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr18:11956846-11957129	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr18:11946810-11947854	K562	blood:	n/a	n/a
38	BACH1	chr18:11980511-11981154	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr18:11937946-11938159	K562	blood:	n/a	n/a
40	BACH1	chr18:11955589-11956009	H1-hESC	embryonic stem cell:	n/a	n/a
41	BATF	chr18:11947213-11947566	GM12878	blood:	n/a	n/a
42	BATF	chr18:11921806-11922227	GM12878	blood:	n/a	n/a
43	BATF	chr18:11947330-11947566	GM12878	blood:	n/a	n/a
44	BATF	chr18:11921744-11922225	GM12878	blood:	n/a	n/a
45	BCL3	chr18:11947164-11947559	A549	lung:	n/a	n/a
46	BCL3	chr18:11947153-11947642	A549	lung:	n/a	n/a
47	BCL3	chr18:11980164-11980758	A549	lung:	n/a	n/a
48	BCL3	chr18:11942734-11943010	GM12878	blood:	n/a	n/a
49	BCL3	chr18:11923291-11923550	GM12878	blood:	n/a	n/a
50	BCLAF1	chr18:11947055-11947530	GM12878	blood:	n/a	n/a

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11981196-11981246	A549	lung:	n/a
2	chr18:11981602-11981652	BJ	skin:	n/a
3	chr18:11947936-11947986	NT2-D1	testis:	n/a
4	chr18:11981602-11981652	HIPEpiC	eye:	n/a
5	chr18:11981389-11981439	SK-N-SH_RA	brain:	n/a
6	chr18:11980981-11981031	HCM	heart:	n/a
7	chr18:11947875-11947925	SK-N-MC	brain:	n/a
8	chr18:11985726-11985776	HRPEpiC	eye:	n/a
9	chr18:11948154-11948204	HPAEpiC	pulmonary alveolar:	n/a
10	chr18:11945273-11945323	AG10803	skin:	n/a
11	chr18:11980297-11980347	GM06990	blood:	n/a
12	chr18:11981196-11981246	AG09319	gingival:	n/a
13	chr18:11980297-11980347	T-47D	breast:	n/a
14	chr18:11947936-11947986	NHBE	bronchial:	n/a
15	chr18:11978319-11978369	Caco-2	colon:	n/a
16	chr18:11981196-11981246	SK-N-MC	brain:	n/a
17	chr18:11982241-11982291	ECC-1	luminal epithelium:	n/a
18	chr18:11980981-11981031	SK-N-SH	brain:	n/a
19	chr18:11947875-11947925	HMEC	breast:	n/a
20	chr18:11948579-11948629	AG09319	gingival:	n/a
21	chr18:11948154-11948204	GM12892	blood:	n/a
22	chr18:11950917-11950967	HRCEpiC	kidney:	n/a
23	chr18:11982063-11982113	K562	blood:	n/a
24	chr18:11948154-11948204	GM12878	blood:	n/a
25	chr18:11982241-11982291	GM12892	blood:	n/a
26	chr18:11981196-11981246	Caco-2	colon:	n/a
27	chr18:11947571-11947621	NT2-D1	testis:	n/a
28	chr18:11980953-11981003	HCM	heart:	n/a
29	chr18:11981317-11981367	HNPCEpiC	eye:	n/a
30	chr18:11981317-11981367	Caco-2	colon:	n/a
31	chr18:11978319-11978369	HNPCEpiC	eye:	n/a
32	chr18:11948579-11948629	HNPCEpiC	eye:	n/a
33	chr18:11950917-11950967	SK-N-MC	brain:	n/a
34	chr18:11981591-11981641	A549	lung:	n/a
35	chr18:11950917-11950967	SK-N-SH	brain:	n/a
36	chr18:11980953-11981003	GM06990	blood:	n/a
37	chr18:11978319-11978369	ProgFib	skin:	n/a
38	chr18:11981317-11981367	HMEC	breast:	n/a
39	chr18:11980953-11981003	HCF	heart:	n/a
40	chr18:11980981-11981031	T-47D	breast:	n/a
41	chr18:11981196-11981246	PFSK-1	brain:	n/a
42	chr18:11981591-11981641	ECC-1	luminal epithelium:	n/a
43	chr18:11947875-11947925	AG09309	skin:	n/a
44	chr18:11947936-11947986	SK-N-MC	brain:	n/a
45	chr18:11947936-11947986	Hepatocyte	liver:	n/a
46	chr18:11980297-11980347	PANC-1	pancreas:	n/a
47	chr18:11947936-11947986	HIPEpiC	eye:	n/a
48	chr18:11982063-11982113	RPTEC	kidney:	n/a
49	chr18:11980953-11981003	AG09309	skin:	n/a
50	chr18:11980690-11980740	MCF-7	breast:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:11947089..11947879-chr19:797034..797866,2	Hela-S3	cervix:
2	chr18:11937505..11938532-chr18:12038635..12039615,5	MCF-7	breast:
3	chr1:28832088..28833058-chr18:11980322..11980977,2	Hela-S3	cervix:
4	chr18:11967810..11971954-chr18:11978967..11982085,5	K562	blood:
5	chr18:11848937..11853647-chr18:11979272..11982109,5	K562	blood:
6	chr18:11945871..11949775-chr18:11972448..11976477,3	K562	blood:
7	chr18:11943801..11947480-chr18:11981525..11984599,3	MCF-7	breast:
8	chr18:11968537..11977808-chr18:11979434..11985075,12	MCF-7	breast:
9	chr18:11947580..11949116-chr18:11949691..11952333,2	K562	blood:
10	chr18:11907153..11910661-chr18:11980045..11982514,4	MCF-7	breast:
11	chr18:11907220..11910223-chr18:11914427..11917601,3	MCF-7	breast:
12	chr18:11972047..11973789-chr18:11978802..11980433,2	MCF-7	breast:
13	chr18:11937557..11938334-chr18:12038177..12039385,5	K562	blood:
14	chr18:11972047..11973789-chr18:11978802..11980433,2	MCF-7	breast:
15	chr18:11979615..11982143-chr18:12376173..12378788,2	K562	blood:
16	chr18:11980301..11981116-chr8:80942163..80942686,2	Hela-S3	cervix:
17	chr18:11978886..11981038-chr18:11986460..11988368,2	MCF-7	breast:
18	chr18:11981635..11982452-chr8:37962701..37963302,2	Hela-S3	cervix:
19	chr18:11941188..11942696-chr18:11979141..11981575,2	K562	blood:
20	chr18:11942200..11944403-chr18:11945957..11947615,2	K562	blood:
21	chr18:11950713..11953292-chr18:11962814..11965398,2	K562	blood:
22	chr1:24285780..24286361-chr18:11980215..11981116,2	Hela-S3	cervix:
23	chr18:11949109..11951046-chr18:11952725..11954944,2	K562	blood:
24	chr18:11908295..11911131-chr18:11922206..11924377,2	K562	blood:
25	chr18:11945202..11946852-chr18:11982600..11984410,2	K562	blood:
26	chr14:24682206..24682834-chr18:11980405..11981236,2	Hela-S3	cervix:
27	chr18:11981732..11982258-chr7:137687279..137688011,2	Hela-S3	cervix:
28	chr18:11978568..11983192-chr18:11993805..11998306,5	MCF-7	breast:
29	chr18:11908235..11908915-chr18:11980031..11980748,2	Hela-S3	cervix:
30	chr18:11947580..11949116-chr18:11949691..11952333,2	K562	blood:
31	chr18:11908313..11910422-chr18:11947484..11949382,3	K562	blood:
32	chr18:11925754..11927617-chr18:11981335..11983833,2	K562	blood:
33	chr18:11908313..11910629-chr18:11947415..11948984,2	K562	blood:
34	chr18:11947304..11948125-chr18:11981391..11982015,2	Hela-S3	cervix:
35	chr18:11949879..11951567-chr18:11988401..11991255,2	K562	blood:
36	chr18:11981504..11983527-chr18:11985199..11986981,3	MCF-7	breast:
37	chr18:11979171..11983679-chr18:11993501..11995734,4	MCF-7	breast:
38	chr12:6579509..6580224-chr18:11980779..11981594,2	Hela-S3	cervix:
39	chr18:11944456..11952400-chr18:11978684..11982486,15	K562	blood:
40	chr18:11979366..11983605-chr18:11984399..11987435,4	MCF-7	breast:
41	chr18:11970057..11972089-chr18:11979053..11982346,3	K562	blood:
42	chr18:11937069..11938706-chr18:11995081..11996087,16	MCF-7	breast:
43	chr18:11905898..11908508-chr18:11980358..11982828,3	K562	blood:
44	chr18:11954134..11957733-chr18:11976816..11981854,6	K562	blood:
45	chr18:11977841..11980802-chr18:11983345..11984923,2	MCF-7	breast:
46	chr18:11851619..11853678-chr18:11981084..11983023,2	MCF-7	breast:
47	chr18:11907115..11909589-chr18:11947697..11950690,2	MCF-7	breast:
48	chr18:11937478..11938603-chr18:11995051..11996237,21	K562	blood:
49	chr18:11938000..11939656-chr18:11946087..11948724,2	K562	blood:
50	chr18:11945202..11946852-chr18:11982600..11984410,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPPE1-1	chr18:11918850-11918913	XLOC_012771
2	lnc-GNAL-2	chr18:11929345-11929475	NONHSAT058332
3	lnc-GNAL-2	chr18:11928837-11929034	NONHSAT058332

No data

Variant related genes	Relation type
ENSG00000267079	TF binding region
ENSG00000267661	TF binding region
IMPA2	TF binding region
ENSG00000267079	CpG island
ENSG00000267661	CpG island
IMPA2	CpG island
ENSG00000185946	chromatin interactions
ENSG00000141401	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000139190	chromatin interactions
ENSG00000267165	chromatin interactions
ENSG00000189266	chromatin interactions
ENSG00000154889	chromatin interactions
ENSG00000254692	chromatin interactions
ENSG00000273141	chromatin interactions
ENSG00000147586	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000117036	chromatin interactions
ENSG00000255112	chromatin interactions
ENSG00000266955	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000267661	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000011304	chromatin interactions
ENSG00000129691	chromatin interactions
ENSG00000141385	chromatin interactions

Extended variants
information (count: 3140 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3140 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4797589	chr18:11917410-11917411	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148262019	chr18:11917417-11917418	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534354143	chr18:11917437-11917438	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs182607670	chr18:11917440-11917441	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs140299393	chr18:11917485-11917486	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543978575	chr18:11917500-11917501	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs4797590	chr18:11917512-11917513	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs552966367	chr18:11917547-11917548	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs577219245	chr18:11917554-11917555	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs187313607	chr18:11917559-11917560	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544634953	chr18:11917583-11917584	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560002168	chr18:11917584-11917585	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527596970	chr18:11917600-11917601	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs79247148	chr18:11917627-11917628	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560929643	chr18:11917657-11917658	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529348108	chr18:11917697-11917698	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115162007	chr18:11917723-11917724	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138102545	chr18:11917724-11917725	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192143164	chr18:11917791-11917792	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185296109	chr18:11917792-11917793	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377744858	chr18:11917819-11917820	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567139874	chr18:11917834-11917835	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62097417	chr18:11917841-11917842	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs62097418	chr18:11917921-11917922	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555886459	chr18:11917925-11917926	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139057520	chr18:11917964-11917965	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs190219764	chr18:11917965-11917966	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs542095	chr18:11917993-11917994	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs555966106	chr18:11918024-11918025	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs577354811	chr18:11918038-11918039	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371783120	chr18:11918077-11918078	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374659913	chr18:11918107-11918108	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs368454301	chr18:11918113-11918114	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs28538701	chr18:11918134-11918135	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs142974823	chr18:11918138-11918139	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs28477865	chr18:11918140-11918141	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs199833320	chr18:11918146-11918147	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374228837	chr18:11918166-11918167	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs71350470	chr18:11918215-11918216	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs553374641	chr18:11918217-11918218	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs146368305	chr18:11918233-11918234	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs571963878	chr18:11918245-11918246	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs542567044	chr18:11918246-11918247	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs28377794	chr18:11918295-11918296	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs375054939	chr18:11918307-11918308	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs5026081	chr18:11918310-11918311	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs5026080	chr18:11918312-11918313	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs544579941	chr18:11918350-11918351	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561278027	chr18:11918375-11918376	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs5026079	chr18:11918376-11918377	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
Melanoma	18172304	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
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1854 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11913800-11920400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr18:11916200-11918000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr18:11916200-11918000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr18:11916400-11917800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr18:11916800-11918000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr18:11916800-11918600	Weak transcription	Primary B cells from cord blood	blood
7	chr18:11917000-11917800	Enhancers	GM12878-XiMat	blood
8	chr18:11917400-11921600	Weak transcription	K562	blood
9	chr18:11917800-11918200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr18:11917800-11921400	Weak transcription	GM12878-XiMat	blood
11	chr18:11918000-11918400	Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr18:11918200-11918600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr18:11918400-11918600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr18:11918600-11918800	Enhancers	Primary B cells from cord blood	blood
15	chr18:11918600-11920200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr18:11918600-11920400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr18:11918800-11919600	Weak transcription	Primary B cells from cord blood	blood
18	chr18:11919600-11919800	Enhancers	Primary B cells from cord blood	blood
19	chr18:11920200-11921400	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr18:11920400-11921600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr18:11920400-11923200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr18:11921400-11921800	Enhancers	Liver	Liver
23	chr18:11921400-11922000	Flanking Active TSS	GM12878-XiMat	blood
24	chr18:11921400-11922200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr18:11921400-11922200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr18:11921600-11922000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr18:11921600-11922000	Enhancers	K562	blood
28	chr18:11921600-11922200	Enhancers	HepG2	liver
29	chr18:11921800-11922000	Flanking Active TSS	Liver	Liver
30	chr18:11921800-11922000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr18:11921800-11922200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr18:11921800-11922200	Enhancers	Hela-S3	cervix
33	chr18:11922000-11922200	Enhancers	GM12878-XiMat	blood
34	chr18:11922000-11922400	Active TSS	Liver	Liver
35	chr18:11922000-11922400	Active TSS	Duodenum Mucosa	Duodenum
36	chr18:11922000-11923400	Weak transcription	K562	blood
37	chr18:11922000-11924000	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr18:11922200-11924000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr18:11922200-11925200	Weak transcription	Hela-S3	cervix
40	chr18:11922200-11925200	Weak transcription	HepG2	liver
41	chr18:11922200-11927200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr18:11923200-11927600	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr18:11923400-11923800	Enhancers	K562	blood
44	chr18:11923800-11925200	Weak transcription	K562	blood
45	chr18:11924000-11925800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr18:11924000-11926200	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr18:11925200-11926400	Enhancers	Hela-S3	cervix
48	chr18:11925200-11927400	Weak transcription	Fetal Lung	lung
49	chr18:11925200-11927600	Enhancers	HepG2	liver
50	chr18:11925200-11927800	Enhancers	K562	blood

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