Variant report

Variant	nsv831150
Chromosome Location	chr7:137500559-137652808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3546)
CpG islands
(count:2198)
Chromatin interactive
region (count:209)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:3546 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:137633213-137634734	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:137619752-137620719	K562	blood:	n/a	n/a
3	ARID3A	chr7:137647650-137648391	K562	blood:	n/a	n/a
4	ARID3A	chr7:137616697-137616940	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:137645946-137646209	K562	blood:	n/a	n/a
6	ARID3A	chr7:137634349-137635034	K562	blood:	n/a	n/a
7	ARID3A	chr7:137578126-137578317	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:137567069-137567448	K562	blood:	n/a	n/a
9	ARID3A	chr7:137651784-137652482	K562	blood:	n/a	n/a
10	ARID3A	chr7:137649277-137650079	K562	blood:	n/a	n/a
11	ARID3A	chr7:137525095-137525187	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:137598976-137599000	K562	blood:	n/a	n/a
13	ARID3A	chr7:137575853-137576316	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:137617717-137617986	K562	blood:	n/a	n/a
15	ARID3A	chr7:137588431-137588809	K562	blood:	n/a	n/a
16	ARID3A	chr7:137628041-137628653	K562	blood:	n/a	n/a
17	ARID3A	chr7:137650554-137651433	K562	blood:	n/a	n/a
18	ARID3A	chr7:137588392-137588635	HepG2	liver:	n/a	n/a
19	ATF1	chr7:137575296-137575643	K562	blood:	n/a	n/a
20	ATF1	chr7:137647566-137648114	K562	blood:	n/a	n/a
21	ATF1	chr7:137651522-137652615	K562	blood:	n/a	n/a
22	ATF1	chr7:137620618-137620937	K562	blood:	n/a	n/a
23	ATF1	chr7:137627794-137628419	K562	blood:	n/a	n/a
24	ATF1	chr7:137650807-137651098	K562	blood:	n/a	n/a
25	ATF1	chr7:137643287-137643956	K562	blood:	n/a	n/a
26	ATF1	chr7:137566974-137567347	K562	blood:	n/a	n/a
27	ATF1	chr7:137649636-137650007	K562	blood:	n/a	n/a
28	ATF1	chr7:137501641-137501750	K562	blood:	n/a	n/a
29	ATF2	chr7:137619868-137620526	GM12878	blood:	n/a	n/a
30	ATF2	chr7:137588224-137588840	GM12878	blood:	n/a	n/a
31	ATF2	chr7:137583873-137584257	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr7:137558188-137558569	GM12878	blood:	n/a	n/a
33	ATF2	chr7:137637797-137638500	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr7:137579854-137580825	GM12878	blood:	n/a	n/a
35	ATF2	chr7:137573042-137573420	GM12878	blood:	n/a	n/a
36	ATF2	chr7:137563936-137564415	GM12878	blood:	n/a	n/a
37	ATF2	chr7:137575057-137575606	GM12878	blood:	n/a	n/a
38	ATF2	chr7:137566876-137567351	GM12878	blood:	n/a	n/a
39	ATF2	chr7:137645865-137646344	GM12878	blood:	n/a	n/a
40	ATF2	chr7:137588348-137588903	GM12878	blood:	n/a	n/a
41	ATF2	chr7:137601995-137602665	GM12878	blood:	n/a	n/a
42	ATF2	chr7:137601266-137602854	GM12878	blood:	n/a	n/a
43	ATF2	chr7:137558163-137558586	GM12878	blood:	n/a	n/a
44	ATF2	chr7:137564091-137564576	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr7:137579712-137581069	GM12878	blood:	n/a	n/a
46	ATF3	chr7:137647666-137648091	K562	blood:	n/a	n/a
47	ATF3	chr7:137627528-137627871	K562	blood:	n/a	n/a
48	ATF3	chr7:137627916-137628383	K562	blood:	n/a	n/a
49	ATF3	chr7:137566917-137567372	K562	blood:	n/a	n/a
50	ATF3	chr7:137566917-137567417	K562	blood:	n/a	n/a

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137557164-137557214	SK-N-SH	brain:	n/a
2	chr7:137624019-137624069	HepG2	liver:	n/a
3	chr7:137557164-137557214	SK-N-SH	brain:	n/a
4	chr7:137624019-137624069	HepG2	liver:	n/a
5	chr7:137637323-137637373	PrEC	prostate:	n/a
6	chr7:137618712-137618762	T-47D	breast:	n/a
7	chr7:137638053-137638103	BJ	skin:	n/a
8	chr7:137531612-137531662	BE2_C	brain:	n/a
9	chr7:137557164-137557214	HRPEpiC	eye:	n/a
10	chr7:137534357-137534407	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:137531612-137531662	AoSMC	blood vessel:	n/a
12	chr7:137605253-137605303	RPTEC	kidney:	n/a
13	chr7:137620868-137620918	NHBE	bronchial:	n/a
14	chr7:137562440-137562490	BJ	skin:	n/a
15	chr7:137564212-137564262	CMK	blood:	n/a
16	chr7:137638053-137638103	HRCEpiC	kidney:	n/a
17	chr7:137559892-137559942	SK-N-SH_RA	brain:	n/a
18	chr7:137620868-137620918	MCF-7	breast:	n/a
19	chr7:137531612-137531662	NHDF-neo	bronchial:	n/a
20	chr7:137559892-137559942	HRPEpiC	eye:	n/a
21	chr7:137531697-137531747	HEK293	kidney:	embryo
22	chr7:137534570-137534620	GM12891	blood:	n/a
23	chr7:137637323-137637373	AG04449	skin:	fetal
24	chr7:137534357-137534407	U87	brain:	n/a
25	chr7:137531258-137531308	HUVEC	blood vessel:	n/a
26	chr7:137605253-137605303	K562	blood:	n/a
27	chr7:137609343-137609393	BJ	skin:	n/a
28	chr7:137638053-137638103	HEEpiC	esophagus:	n/a
29	chr7:137531173-137531223	H1-hESC	embryonic stem cell:	embryo
30	chr7:137531173-137531223	Hepatocyte	liver:	n/a
31	chr7:137651542-137651592	HEEpiC	esophagus:	n/a
32	chr7:137529886-137529936	ECC-1	luminal epithelium:	n/a
33	chr7:137562440-137562490	BE2_C	brain:	n/a
34	chr7:137534357-137534407	NHBE	bronchial:	n/a
35	chr7:137505606-137505656	LNCaP	prostate:	n/a
36	chr7:137529886-137529936	HUVEC	blood vessel:	n/a
37	chr7:137620397-137620447	NHDF-neo	bronchial:	n/a
38	chr7:137531173-137531223	PFSK-1	brain:	n/a
39	chr7:137620868-137620918	HRPEpiC	eye:	n/a
40	chr7:137620868-137620918	HIPEpiC	eye:	n/a
41	chr7:137531697-137531747	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:137532374-137532424	GM12878	blood:	n/a
43	chr7:137532857-137532907	NHDF-neo	bronchial:	n/a
44	chr7:137545862-137545912	SK-N-SH	brain:	n/a
45	chr7:137531952-137532002	A549	lung:	n/a
46	chr7:137531952-137532002	MCF10A-Er-Src	breast:	n/a
47	chr7:137620397-137620447	Jurkat	blood:	n/a
48	chr7:137646869-137646919	AG04450	lung:	fetal
49	chr7:137605253-137605303	PANC-1	pancreas:	n/a
50	chr7:137570950-137571000	HIPEpiC	eye:	n/a

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:137590712..137592548-chr7:137594449..137596877,2	K562	blood:
2	chr7:137569917..137572586-chr7:137572838..137575553,3	K562	blood:
3	chr7:137648208..137650009-chr7:137671387..137674273,2	MCF-7	breast:
4	chr7:137650568..137655149-chr7:137681332..137686254,5	K562	blood:
5	chr7:137525647..137527240-chr7:137529782..137531932,2	K562	blood:
6	chr7:137588115..137589486-chr7:137686760..137687662,5	K562	blood:
7	chr7:137340756..137341673-chr7:137583558..137584733,6	MCF-7	breast:
8	chr7:137619156..137621856-chr7:137650615..137653310,2	MCF-7	breast:
9	chr7:137588092..137589015-chr7:137746698..137747545,2	K562	blood:
10	chr7:137340758..137342211-chr7:137583440..137584629,9	MCF-7	breast:
11	chr7:137646546..137650586-chr7:137681825..137685474,4	MCF-7	breast:
12	chr7:137620168..137621846-chr7:137623700..137626526,2	K562	blood:
13	chr7:137611909..137614588-chr7:137616790..137618864,2	K562	blood:
14	chr7:137633876..137635550-chr7:137637244..137638780,2	MCF-7	breast:
15	chr7:137588477..137590642-chr7:137638045..137640393,3	MCF-7	breast:
16	chr7:137584438..137586090-chr7:137588352..137591212,2	MCF-7	breast:
17	chr7:137646686..137649675-chr7:137664959..137667243,4	MCF-7	breast:
18	chr7:137642477..137645042-chr7:137646430..137648183,3	MCF-7	breast:
19	chr7:137619037..137621217-chr7:137637185..137638746,2	MCF-7	breast:
20	chr7:137643171..137645975-chr7:137687593..137689334,2	K562	blood:
21	chr7:137619156..137621856-chr7:137650615..137653310,2	MCF-7	breast:
22	chr7:137594343..137597312-chr7:137601337..137603443,2	K562	blood:
23	chr3:156876358..156877967-chr7:137583930..137585430,2	MCF-7	breast:
24	chr7:137593114..137594861-chr7:137623750..137626523,2	MCF-7	breast:
25	chr7:137641810..137644314-chr7:137677657..137679366,2	K562	blood:
26	chr7:137505132..137508023-chr7:137518850..137521605,2	K562	blood:
27	chr7:137521731..137523551-chr7:137529090..137530870,2	K562	blood:
28	chr7:137575157..137577662-chr7:137579588..137582009,3	K562	blood:
29	chr7:137600305..137602461-chr7:137615591..137618449,2	MCF-7	breast:
30	chr7:137620870..137622447-chr7:137627955..137630199,2	K562	blood:
31	chr7:137647183..137649152-chr7:137686231..137688574,2	MCF-7	breast:
32	chr7:137506372..137508298-chr7:137508661..137511355,2	K562	blood:
33	chr7:137554665..137556527-chr7:137556593..137558804,2	K562	blood:
34	chr7:137290258..137291771-chr7:137583549..137584521,7	MCF-7	breast:
35	chr7:137583612..137584186-chr7:137693303..137693962,2	MCF-7	breast:
36	chr7:137611909..137614588-chr7:137616790..137618864,2	K562	blood:
37	chr7:137652427..137654026-chr7:137674735..137676938,2	K562	blood:
38	chr7:137550548..137553249-chr7:137557181..137559857,2	MCF-7	breast:
39	chr7:137587845..137589721-chr7:137692660..137694705,36	K562	blood:
40	chr7:137527969..137530649-chr7:137533553..137535061,2	MCF-7	breast:
41	chr7:137636438..137645214-chr7:137681826..137688964,19	MCF-7	breast:
42	chr7:137587289..137589921-chr7:137595716..137597965,2	MCF-7	breast:
43	chr7:137620870..137622447-chr7:137627955..137630199,2	K562	blood:
44	chr7:137527969..137530649-chr7:137533553..137535061,2	MCF-7	breast:
45	chr7:137641810..137650191-chr7:137677657..137683130,9	K562	blood:
46	chr7:137504613..137507167-chr7:137508809..137511405,2	K562	blood:
47	chr7:137650743..137652751-chr7:137656187..137658700,3	K562	blood:
48	chr7:137587289..137589921-chr7:137595716..137597965,2	MCF-7	breast:
49	chr7:137652166..137654948-chr7:137667610..137670033,2	K562	blood:
50	chr7:137617208..137619584-chr7:137640334..137642148,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1D1-5	chr7:137531776-137533814	NONHSAT123588
2	lnc-AKR1D1-2	chr7:137638094-137638270	ENSG00000237243.1
3	lnc-AKR1D1-2	chr7:137639994-137640082	ENSG00000237243.1
4	lnc-AKR1D1-2	chr7:137641330-137641391	ENSG00000237243.1
5	lnc-AKR1D1-2	chr7:137642464-137642712	ENSG00000237243.1

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CREB3L2	hsa-miR-92a-3p	chr7:137564628-137564622
2	CREB3L2	hsa-miR-19b-3p	chr7:137562062-137562086
3	CREB3L2	hsa-miR-124-3p	chr7:137561047-137561040
4	CREB3L2	hsa-miR-19b-3p	chr7:137560878-137560900
5	CREB3L2	hsa-miR-124-3p	chr7:137561036-137561029
6	CREB3L2	hsa-miR-124-3p	chr7:137561041-137561061
7	CREB3L2	hsa-miR-92a-3p	chr7:137560823-137560817
8	CREB3L2	hsa-miR-124-3p	chr7:137561030-137561049

Variant related genes	Relation type
CREB3L2	TF binding region
DGKI	TF binding region
ENSG00000237243	TF binding region
CREB3L2	CpG island
DGKI	CpG island
ENSG00000237243	CpG island
ENSG00000199004	chromatin interactions
ENSG00000122787	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000237243	chromatin interactions
ENSG00000157680	chromatin interactions
ENSG00000182158	chromatin interactions

Extended variants
information (count: 5677 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5677 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145646703	chr7:137500582-137500583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534980469	chr7:137500601-137500602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546379462	chr7:137500609-137500610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554685675	chr7:137500611-137500612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145153272	chr7:137500624-137500625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543495472	chr7:137500741-137500742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563481020	chr7:137500839-137500840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376793903	chr7:137500857-137500858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115319997	chr7:137500897-137500898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572277426	chr7:137500981-137500982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149112473	chr7:137501043-137501044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143184337	chr7:137501046-137501047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559564629	chr7:137501067-137501068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528397657	chr7:137501110-137501111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548492983	chr7:137501152-137501153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561514719	chr7:137501191-137501192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530571334	chr7:137501256-137501257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112678968	chr7:137501354-137501355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148257746	chr7:137501385-137501386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532710708	chr7:137501386-137501387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552817786	chr7:137501431-137501432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566332492	chr7:137501450-137501451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6950955	chr7:137501468-137501469	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs561373928	chr7:137501511-137501512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371373962	chr7:137501518-137501519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537094202	chr7:137501532-137501533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577904459	chr7:137501559-137501560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556988743	chr7:137501577-137501578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543544236	chr7:137501604-137501605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78486021	chr7:137501780-137501781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs80180262	chr7:137501781-137501782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545565938	chr7:137501782-137501783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528856227	chr7:137501784-137501785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80010612	chr7:137501801-137501802	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192953072	chr7:137501840-137501841	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550302805	chr7:137501841-137501842	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368955435	chr7:137501854-137501855	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368372580	chr7:137501867-137501868	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563331322	chr7:137501897-137501898	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530472828	chr7:137501908-137501909	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544234179	chr7:137501921-137501922	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564133599	chr7:137501925-137501926	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528912425	chr7:137501931-137501932	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34899996	chr7:137501962-137501963	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548965593	chr7:137501984-137501985	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548934634	chr7:137501993-137501994	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112256828	chr7:137502055-137502056	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528723772	chr7:137502077-137502078	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562840447	chr7:137502084-137502085	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559060776	chr7:137502117-137502118	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:6192 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137486000-137501800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:137486600-137501800	Weak transcription	HSMMtube	muscle
3	chr7:137490200-137501600	Weak transcription	Osteobl	bone
4	chr7:137490200-137504600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr7:137490200-137505200	Weak transcription	NH-A	brain
6	chr7:137490400-137501000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr7:137490400-137505200	Weak transcription	HSMM	muscle
8	chr7:137494000-137505600	Weak transcription	Aorta	Aorta
9	chr7:137494400-137504400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:137498200-137504400	Weak transcription	Fetal Brain Female	brain
11	chr7:137498800-137500800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:137499000-137501000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:137499200-137501000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:137499200-137501200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:137499400-137504400	Weak transcription	Fetal Brain Male	brain
16	chr7:137499800-137501800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr7:137500800-137503200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:137501000-137501800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:137501000-137503400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:137501000-137503800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr7:137501200-137503400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:137501400-137501800	Enhancers	Brain Angular Gyrus	brain
23	chr7:137501400-137502000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:137501400-137502000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:137501600-137501800	Enhancers	Brain Anterior Caudate	brain
26	chr7:137501600-137502000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:137501600-137502000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:137501600-137502000	Enhancers	HepG2	liver
29	chr7:137501600-137502200	Enhancers	NHLF	lung
30	chr7:137501600-137503200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:137501600-137504200	Enhancers	Osteobl	bone
32	chr7:137501800-137502000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:137501800-137502000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:137501800-137502000	Enhancers	Brain Cingulate Gyrus	brain
35	chr7:137501800-137502600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:137501800-137502800	Weak transcription	Brain Anterior Caudate	brain
37	chr7:137501800-137503400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr7:137501800-137503400	Enhancers	HSMMtube	muscle
39	chr7:137501800-137503400	Enhancers	NHDF-Ad	bronchial
40	chr7:137501800-137505000	Weak transcription	Brain Angular Gyrus	brain
41	chr7:137502000-137503800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:137502000-137503800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr7:137502000-137504400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr7:137502000-137504600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:137502000-137504600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:137502000-137504800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr7:137502000-137505000	Weak transcription	Brain Cingulate Gyrus	brain
48	chr7:137502200-137502600	Weak transcription	NHLF	lung
49	chr7:137502400-137503200	Enhancers	Adipose Nuclei	Adipose
50	chr7:137502600-137502800	Enhancers	GM12878-XiMat	blood

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