Variant report

Variant	nsv470453
Chromosome Location	chr2:37669487-37868214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3478)
CpG islands
(count:854)
Chromatin interactive
region (count:89)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3478 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37813485-37813599	K562	blood:	n/a	n/a
2	ARID3A	chr2:37788399-37789814	K562	blood:	n/a	n/a
3	ARID3A	chr2:37843852-37844052	K562	blood:	n/a	n/a
4	ARID3A	chr2:37860715-37860729	K562	blood:	n/a	n/a
5	ARID3A	chr2:37791509-37791839	K562	blood:	n/a	n/a
6	ATF1	chr2:37858521-37859005	K562	blood:	n/a	n/a
7	ATF1	chr2:37788766-37789778	K562	blood:	n/a	n/a
8	ATF1	chr2:37843821-37844106	K562	blood:	n/a	n/a
9	ATF1	chr2:37683295-37683405	K562	blood:	n/a	n/a
10	ATF1	chr2:37795814-37796120	K562	blood:	n/a	n/a
11	ATF1	chr2:37785928-37786123	K562	blood:	n/a	n/a
12	ATF1	chr2:37751020-37751314	K562	blood:	n/a	n/a
13	ATF1	chr2:37813344-37813675	K562	blood:	n/a	n/a
14	ATF1	chr2:37680213-37680384	K562	blood:	n/a	n/a
15	ATF1	chr2:37688108-37688338	K562	blood:	n/a	n/a
16	ATF2	chr2:37801045-37801610	GM12878	blood:	n/a	n/a
17	ATF2	chr2:37856610-37857037	GM12878	blood:	n/a	n/a
18	ATF2	chr2:37827809-37828379	GM12878	blood:	n/a	n/a
19	ATF2	chr2:37797556-37799195	GM12878	blood:	n/a	chr2:37798092-37798099
20	ATF2	chr2:37857759-37858362	GM12878	blood:	n/a	n/a
21	ATF2	chr2:37800861-37801410	GM12878	blood:	n/a	n/a
22	ATF2	chr2:37856482-37857126	GM12878	blood:	n/a	n/a
23	ATF2	chr2:37733520-37733938	GM12878	blood:	n/a	n/a
24	ATF2	chr2:37776602-37777831	GM12878	blood:	n/a	n/a
25	ATF2	chr2:37797402-37799149	GM12878	blood:	n/a	chr2:37798092-37798099
26	ATF2	chr2:37785796-37786291	GM12878	blood:	n/a	n/a
27	ATF2	chr2:37777167-37777705	GM12878	blood:	n/a	n/a
28	ATF2	chr2:37862185-37863679	GM12878	blood:	n/a	n/a
29	ATF2	chr2:37857844-37858344	GM12878	blood:	n/a	n/a
30	ATF2	chr2:37813152-37813759	GM12878	blood:	n/a	n/a
31	ATF2	chr2:37850974-37852084	GM12878	blood:	n/a	n/a
32	ATF2	chr2:37852754-37853735	GM12878	blood:	n/a	n/a
33	ATF2	chr2:37772609-37773228	GM12878	blood:	n/a	n/a
34	ATF2	chr2:37785747-37786347	GM12878	blood:	n/a	n/a
35	ATF2	chr2:37772606-37773191	GM12878	blood:	n/a	n/a
36	ATF2	chr2:37850936-37852115	GM12878	blood:	n/a	n/a
37	ATF2	chr2:37862323-37863607	GM12878	blood:	n/a	n/a
38	ATF3	chr2:37788654-37789254	K562	blood:	n/a	n/a
39	ATF3	chr2:37788706-37789086	GM12878	blood:	n/a	n/a
40	ATF3	chr2:37788765-37789063	K562	blood:	n/a	n/a
41	ATF3	chr2:37788816-37789002	GM12878	blood:	n/a	n/a
42	ATF3	chr2:37843784-37844144	K562	blood:	n/a	n/a
43	ATF3	chr2:37862785-37862993	GM12878	blood:	n/a	n/a
44	ATF3	chr2:37789375-37789814	K562	blood:	n/a	n/a
45	BACH1	chr2:37788843-37789230	K562	blood:	n/a	n/a
46	BATF	chr2:37827908-37828305	GM12878	blood:	n/a	chr2:37828080-37828091 chr2:37828085-37828095
47	BATF	chr2:37850556-37851920	GM12878	blood:	n/a	n/a
48	BATF	chr2:37856608-37857021	GM12878	blood:	n/a	n/a
49	BATF	chr2:37862299-37863295	GM12878	blood:	n/a	chr2:37862792-37862803
50	BATF	chr2:37829880-37830187	GM12878	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37734390-37734440	NT2-D1	testis:	n/a
2	chr2:37853482-37853532	SK-N-SH_RA	brain:	n/a
3	chr2:37787889-37787939	HCF	heart:	n/a
4	chr2:37816339-37816389	MCF10A-Er-Src	breast:	n/a
5	chr2:37699716-37699766	SK-N-SH_RA	brain:	n/a
6	chr2:37841934-37841984	HRE	kidney:	n/a
7	chr2:37684473-37684523	GM06990	blood:	n/a
8	chr2:37798344-37798394	ProgFib	skin:	n/a
9	chr2:37751449-37751499	ECC-1	luminal epithelium:	n/a
10	chr2:37816339-37816389	AoSMC	blood vessel:	n/a
11	chr2:37790618-37790668	HCPEpiC	choroid plexus:	n/a
12	chr2:37815128-37815178	H1-hESC	embryonic stem cell:	embryo
13	chr2:37787889-37787939	Hepatocyte	liver:	n/a
14	chr2:37790618-37790668	ProgFib	skin:	n/a
15	chr2:37815128-37815178	HepG2	liver:	n/a
16	chr2:37816339-37816389	HNPCEpiC	eye:	n/a
17	chr2:37798344-37798394	GM12878	blood:	n/a
18	chr2:37787889-37787939	AG09309	skin:	n/a
19	chr2:37699716-37699766	HMEC	breast:	n/a
20	chr2:37790618-37790668	MCF10A-Er-Src	breast:	n/a
21	chr2:37703400-37703450	HCT-116	colon:	n/a
22	chr2:37841934-37841984	SK-N-SH_RA	brain:	n/a
23	chr2:37813553-37813603	GM12878	blood:	n/a
24	chr2:37815128-37815178	HMEC	breast:	n/a
25	chr2:37790618-37790668	HRPEpiC	eye:	n/a
26	chr2:37862761-37862811	GM12892	blood:	n/a
27	chr2:37798344-37798394	BE2_C	brain:	n/a
28	chr2:37853482-37853532	Jurkat	blood:	n/a
29	chr2:37841934-37841984	HMEC	breast:	n/a
30	chr2:37751449-37751499	SK-N-SH	brain:	n/a
31	chr2:37841934-37841984	SK-N-SH	brain:	n/a
32	chr2:37815128-37815178	AG09309	skin:	n/a
33	chr2:37816339-37816389	AG10803	skin:	n/a
34	chr2:37734390-37734440	NHBE	bronchial:	n/a
35	chr2:37862761-37862811	RPTEC	kidney:	n/a
36	chr2:37684473-37684523	A549	lung:	n/a
37	chr2:37751449-37751499	H1-hESC	embryonic stem cell:	embryo
38	chr2:37862761-37862811	SK-N-SH_RA	brain:	n/a
39	chr2:37841934-37841984	ovcar-3	ovarian:	n/a
40	chr2:37813553-37813603	HRCEpiC	kidney:	n/a
41	chr2:37787889-37787939	CMK	blood:	n/a
42	chr2:37751449-37751499	HL-60	blood:	n/a
43	chr2:37734390-37734440	IMR90	lung:	fetal
44	chr2:37684473-37684523	H1-hESC	embryonic stem cell:	embryo
45	chr2:37798344-37798394	SAEC	small airway:	n/a
46	chr2:37841934-37841984	HCM	heart:	n/a
47	chr2:37853482-37853532	Hepatocyte	liver:	n/a
48	chr2:37734390-37734440	HCF	heart:	n/a
49	chr2:37699716-37699766	HCT-116	colon:	n/a
50	chr2:37734390-37734440	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:37700411..37701975-chr2:37710008..37711802,2	MCF-7	breast:
2	chr2:37762322..37765229-chr2:37766980..37769803,2	MCF-7	breast:
3	chr2:37810708..37813206-chr2:37814020..37815979,2	K562	blood:
4	chr2:37839740..37841439-chr2:37842697..37845685,2	K562	blood:
5	chr2:37693807..37696751-chr2:37697172..37699448,2	MCF-7	breast:
6	chr2:37810267..37812004-chr2:37812621..37814787,2	MCF-7	breast:
7	chr2:37712267..37714639-chr2:37715187..37717308,2	MCF-7	breast:
8	chr2:37765925..37767453-chr2:37769359..37772141,2	K562	blood:
9	chr2:37858708..37861309-chr2:37897496..37899960,2	MCF-7	breast:
10	chr2:37816065..37817832-chr2:37818694..37820590,2	MCF-7	breast:
11	chr2:37860309..37862165-chr2:37866082..37868468,2	K562	blood:
12	chr2:37799670..37802467-chr2:37802654..37804539,2	MCF-7	breast:
13	chr2:37816065..37817832-chr2:37818694..37820590,2	MCF-7	breast:
14	chr2:37859378..37862018-chr2:37863759..37867582,3	K562	blood:
15	chr2:37795029..37797811-chr2:37802354..37805859,3	K562	blood:
16	chr2:37710296..37713273-chr2:37733233..37735732,2	MCF-7	breast:
17	chr2:37865948..37868247-chr2:37870789..37872523,2	K562	blood:
18	chr2:37678097..37679683-chr2:37681687..37683352,2	K562	blood:
19	chr2:37781860..37785625-chr2:37786304..37788972,4	K562	blood:
20	chr2:37678097..37679683-chr2:37681687..37683352,2	K562	blood:
21	chr2:37748769..37750538-chr2:37760905..37763616,2	K562	blood:
22	chr2:37789512..37791972-chr2:37800860..37802829,2	K562	blood:
23	chr2:37782232..37784356-chr2:37804122..37805641,2	MCF-7	breast:
24	chr2:37748014..37749874-chr2:37757456..37760173,2	MCF-7	breast:
25	chr2:37860354..37862423-chr2:37867033..37868574,2	MCF-7	breast:
26	chr2:37853940..37855732-chr2:37858093..37860839,2	K562	blood:
27	chr2:37776380..37779203-chr2:37779985..37783372,3	K562	blood:
28	chr2:37682465..37684139-chr2:37686739..37688333,2	K562	blood:
29	chr2:37859378..37862018-chr2:37863759..37867582,3	K562	blood:
30	chr2:37786608..37790547-chr2:37791244..37795872,7	K562	blood:
31	chr2:37789729..37791788-chr2:37804945..37807693,2	K562	blood:
32	chr2:37847422..37850063-chr2:37852020..37854962,2	K562	blood:
33	chr2:37795029..37797811-chr2:37802354..37805859,3	K562	blood:
34	chr2:37839740..37841439-chr2:37842697..37845685,2	K562	blood:
35	chr2:37789512..37791972-chr2:37800860..37802829,2	K562	blood:
36	chr2:37748014..37749874-chr2:37757456..37760173,2	MCF-7	breast:
37	chr2:37700411..37701975-chr2:37710008..37711802,2	MCF-7	breast:
38	chr2:37728444..37730701-chr2:37746195..37748553,2	MCF-7	breast:
39	chr2:37813986..37816982-chr2:37818783..37822459,3	K562	blood:
40	chr2:37860354..37862423-chr2:37867033..37868574,2	MCF-7	breast:
41	chr2:37853880..37855440-chr2:37859339..37862241,2	K562	blood:
42	chr2:37853940..37855732-chr2:37858093..37860839,2	K562	blood:
43	chr2:37712267..37714639-chr2:37715187..37717308,2	MCF-7	breast:
44	chr2:37791325..37795155-chr2:37795900..37799036,5	K562	blood:
45	chr2:37828090..37830166-chr2:37831217..37833289,2	K562	blood:
46	chr2:37866118..37867665-chr2:37869743..37872565,2	MCF-7	breast:
47	chr2:37847066..37848663-chr2:37853249..37855313,2	MCF-7	breast:
48	chr2:37785013..37788185-chr2:37797266..37800761,3	K562	blood:
49	chr2:37813986..37816982-chr2:37818783..37822459,3	K562	blood:
50	chr2:37796095..37797959-chr2:37798225..37800388,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC42EP3-4	chr2:37789433-37789882	NONHSAT070125
2	lnc-QPCT-3	chr2:37839316-37839401	ENSG00000236213.1
3	lnc-QPCT-3	chr2:37831452-37831572	NONHSAT070127
4	lnc-QPCT-3	chr2:37827065-37827505	XLOC_001430
5	lnc-QPCT-3	chr2:37826300-37827505	NONHSAT070127
6	lnc-QPCT-3	chr2:37831452-37831877	XLOC_001430
7	lnc-QPCT-4	chr2:37827621-37827693	NONHSAT070126
8	lnc-QPCT-2	chr2:37716639-37716724	XLOC_001429
9	lnc-QPCT-4	chr2:37824980-37825290	NONHSAT070126
10	lnc-QPCT-3	chr2:37864557-37865599	NONHSAT070132
11	lnc-QPCT-2	chr2:37764138-37764397	XLOC_001429
12	lnc-QPCT-3	chr2:37827279-37827505	ENSG00000236213.1
13	lnc-QPCT-3	chr2:37839316-37839573	XLOC_001430
14	lnc-QPCT-3	chr2:37832379-37870742	NONHSAT070127
15	lnc-QPCT-3	chr2:37827040-37827505	XLOC_001430

No data

Variant related genes	Relation type
ENSG00000236213	TF binding region
ENSG00000236213	CpG island
ENSG00000206737	chromatin interactions
ENSG00000163171	chromatin interactions
LIMCH1	miRNA target sites

Extended variants
information (count: 8813 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:8813 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4670719	chr2:37669487-37669488	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181716564	chr2:37669489-37669490	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535480613	chr2:37669521-37669522	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185590089	chr2:37669547-37669548	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565804816	chr2:37669581-37669582	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113921127	chr2:37669659-37669660	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539520781	chr2:37669712-37669713	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557861073	chr2:37669730-37669731	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576723313	chr2:37669732-37669733	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115368150	chr2:37669741-37669742	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556025651	chr2:37669746-37669747	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146906628	chr2:37669768-37669769	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147944329	chr2:37669784-37669785	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559585439	chr2:37669788-37669789	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541455865	chr2:37669800-37669801	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559472270	chr2:37669917-37669918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190045262	chr2:37669939-37669940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545119711	chr2:37669972-37669973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563402070	chr2:37669998-37669999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531406475	chr2:37670067-37670068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150446958	chr2:37670072-37670073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568384386	chr2:37670092-37670093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34286933	chr2:37670093-37670094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529162702	chr2:37670097-37670098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74433712	chr2:37670100-37670101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565562992	chr2:37670102-37670103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180906131	chr2:37670132-37670133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138263430	chr2:37670150-37670151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569718783	chr2:37670152-37670153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537686347	chr2:37670181-37670182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541909126	chr2:37670266-37670267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76361394	chr2:37670295-37670296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9917152	chr2:37670320-37670321	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556000654	chr2:37670393-37670394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184890474	chr2:37670430-37670431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553601145	chr2:37670451-37670452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577626459	chr2:37670453-37670454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549450691	chr2:37670458-37670459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191993305	chr2:37670477-37670478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184204862	chr2:37670530-37670531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575326587	chr2:37670569-37670570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72881567	chr2:37670587-37670588	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs73924662	chr2:37670592-37670593	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs75184695	chr2:37670594-37670595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115572808	chr2:37670602-37670603	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76031952	chr2:37670608-37670609	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551390051	chr2:37670641-37670642	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569804960	chr2:37670656-37670657	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537126611	chr2:37670701-37670702	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564663634	chr2:37670720-37670721	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3476 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37668200-37669800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:37669200-37675200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:37669600-37670000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:37669800-37670000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:37670000-37670600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:37670000-37678400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:37670400-37670800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:37670400-37671000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:37670600-37671000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:37671000-37671200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:37672800-37676600	Weak transcription	Aorta	Aorta
12	chr2:37674200-37674600	Active TSS	HSMM	muscle
13	chr2:37674600-37674800	Enhancers	Fetal Muscle Leg	muscle
14	chr2:37674600-37674800	Enhancers	Psoas Muscle	Psoas
15	chr2:37674600-37676600	Weak transcription	HSMM	muscle
16	chr2:37674800-37683600	Weak transcription	Psoas Muscle	Psoas
17	chr2:37675200-37675400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:37675200-37675400	Enhancers	Fetal Kidney	kidney
19	chr2:37675400-37676000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:37675400-37676400	Weak transcription	Fetal Kidney	kidney
21	chr2:37675400-37678000	Enhancers	Osteobl	bone
22	chr2:37675800-37676800	Enhancers	Fetal Heart	heart
23	chr2:37675800-37678600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr2:37676000-37676200	Enhancers	Ovary	ovary
25	chr2:37676000-37677000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:37676000-37678400	Enhancers	Primary hematopoietic stem cells	blood
27	chr2:37676000-37678600	Enhancers	Fetal Thymus	thymus
28	chr2:37676200-37676400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:37676200-37677400	Weak transcription	Ovary	ovary
30	chr2:37676200-37678600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:37676400-37677200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr2:37676400-37678200	Enhancers	Fetal Kidney	kidney
33	chr2:37676600-37676800	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr2:37676600-37676800	Enhancers	HSMM	muscle
35	chr2:37676600-37677000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr2:37676600-37677000	Enhancers	Fetal Lung	lung
37	chr2:37676600-37677000	Enhancers	HSMMtube	muscle
38	chr2:37676600-37677400	Enhancers	Rectal Smooth Muscle	rectum
39	chr2:37676600-37677600	Enhancers	NH-A	brain
40	chr2:37676600-37677800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:37676600-37677800	Enhancers	Aorta	Aorta
42	chr2:37676600-37677800	Enhancers	HUVEC	blood vessel
43	chr2:37676800-37677000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr2:37676800-37677200	Enhancers	Fetal Muscle Leg	muscle
45	chr2:37676800-37677400	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr2:37676800-37677600	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr2:37676800-37677600	Enhancers	Fetal Stomach	stomach
48	chr2:37676800-37677800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr2:37676800-37679400	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr2:37676800-37682000	Weak transcription	Fetal Heart	heart

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