Variant report

Variant	esv2753059
Chromosome Location	chr7:136633745-136893745
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:927)
CpG islands
(count:1404)
Chromatin interactive
region (count:33)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:927 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:136853987-136854164	HepG2	liver:	n/a	n/a
2	ATF1	chr7:136641171-136641199	K562	blood:	n/a	n/a
3	ATF2	chr7:136853857-136854307	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:136853848-136854381	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:136805457-136805800	GM12878	blood:	n/a	n/a
6	ATF2	chr7:136805453-136805858	GM12878	blood:	n/a	n/a
7	BACH1	chr7:136880793-136881122	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:136853886-136854162	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:136880818-136881042	K562	blood:	n/a	n/a
10	BATF	chr7:136805497-136805854	GM12878	blood:	n/a	n/a
11	BATF	chr7:136805425-136805782	GM12878	blood:	n/a	n/a
12	BATF	chr7:136657706-136658090	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:136805462-136805767	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:136657748-136657993	GM12878	blood:	n/a	n/a
15	BCL3	chr7:136805413-136805833	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:136856791-136856855	GM12878	blood:	n/a	n/a
17	CCNT2	chr7:136730546-136730666	K562	blood:	n/a	n/a
18	CCNT2	chr7:136675411-136675474	K562	blood:	n/a	n/a
19	CCNT2	chr7:136801095-136801248	K562	blood:	n/a	n/a
20	CEBPB	chr7:136698816-136699059	HepG2	liver:	n/a	chr7:136698927-136698938 chr7:136698926-136698937
21	CEBPB	chr7:136682481-136682821	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:136710206-136710571	IMR90	lung:	n/a	chr7:136710510-136710521
23	CEBPB	chr7:136766179-136766912	IMR90	lung:	n/a	chr7:136766397-136766409
24	CEBPB	chr7:136677486-136677982	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:136835316-136835641	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:136756407-136756758	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:136815566-136815985	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:136795324-136795741	IMR90	lung:	n/a	chr7:136795557-136795568 chr7:136795505-136795518 chr7:136795506-136795517 chr7:136795682-136795693
29	CEBPB	chr7:136755399-136756035	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:136677453-136677945	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:136700215-136700661	HepG2	liver:	n/a	chr7:136700504-136700515
32	CEBPB	chr7:136795393-136795679	Hela-S3	cervix:	n/a	chr7:136795557-136795568 chr7:136795505-136795518 chr7:136795506-136795517
33	CEBPB	chr7:136754070-136754357	HepG2	liver:	n/a	chr7:136754184-136754195 chr7:136754211-136754222 chr7:136754209-136754222
34	CEBPB	chr7:136700107-136700662	IMR90	lung:	n/a	chr7:136700504-136700515
35	CEBPB	chr7:136798395-136798648	HepG2	liver:	n/a	chr7:136798521-136798532
36	CEBPB	chr7:136830658-136831982	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:136677595-136677628	K562	blood:	n/a	n/a
38	CEBPB	chr7:136640841-136641791	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:136691088-136691476	IMR90	lung:	n/a	chr7:136691278-136691289
40	CEBPB	chr7:136856746-136856949	IMR90	lung:	n/a	chr7:136856865-136856876
41	CEBPB	chr7:136851292-136851308	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:136757782-136759597	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:136793847-136793985	A549	lung:	n/a	chr7:136793938-136793949
44	CEBPB	chr7:136795406-136795705	A549	lung:	n/a	chr7:136795557-136795568 chr7:136795505-136795518 chr7:136795506-136795517 chr7:136795682-136795693
45	CEBPB	chr7:136798486-136798602	K562	blood:	n/a	chr7:136798521-136798532
46	CEBPB	chr7:136812624-136812919	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:136853989-136854249	H1-hESC	embryonic stem cell:	n/a	chr7:136854153-136854165
48	CEBPB	chr7:136642576-136642955	IMR90	lung:	n/a	chr7:136642764-136642781 chr7:136642765-136642778
49	CEBPB	chr7:136731406-136731664	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:136642644-136642887	Hela-S3	cervix:	n/a	chr7:136642764-136642781 chr7:136642765-136642778

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:136849187-136849237	PrEC	prostate:	n/a
2	chr7:136849187-136849237	PrEC	prostate:	n/a
3	chr7:136671798-136671848	CMK	blood:	n/a
4	chr7:136849018-136849068	HCT-116	colon:	n/a
5	chr7:136648231-136648281	HCF	heart:	n/a
6	chr7:136700699-136700749	PANC-1	pancreas:	n/a
7	chr7:136683107-136683157	IMR90	lung:	fetal
8	chr7:136683107-136683157	HRCEpiC	kidney:	n/a
9	chr7:136700699-136700749	AG04449	skin:	fetal
10	chr7:136683107-136683157	AG04449	skin:	fetal
11	chr7:136768089-136768139	Caco-2	colon:	n/a
12	chr7:136671798-136671848	A549	lung:	n/a
13	chr7:136700699-136700749	NB4	blood:	n/a
14	chr7:136832262-136832312	K562	blood:	n/a
15	chr7:136849143-136849193	HCT-116	colon:	n/a
16	chr7:136686832-136686882	HCM	heart:	n/a
17	chr7:136845265-136845315	RPTEC	kidney:	n/a
18	chr7:136700699-136700749	HCT-116	colon:	n/a
19	chr7:136648231-136648281	HEEpiC	esophagus:	n/a
20	chr7:136879401-136879451	HNPCEpiC	eye:	n/a
21	chr7:136671798-136671848	HNPCEpiC	eye:	n/a
22	chr7:136691229-136691279	SAEC	small airway:	n/a
23	chr7:136685094-136685144	NT2-D1	testis:	n/a
24	chr7:136701166-136701216	T-47D	breast:	n/a
25	chr7:136849262-136849312	Jurkat	blood:	n/a
26	chr7:136849143-136849193	GM12892	blood:	n/a
27	chr7:136698566-136698616	HEK293	kidney:	embryo
28	chr7:136768089-136768139	SK-N-SH_RA	brain:	n/a
29	chr7:136794953-136795003	A549	lung:	n/a
30	chr7:136849187-136849237	Hela-S3	cervix:	n/a
31	chr7:136766058-136766108	Hepatocyte	liver:	n/a
32	chr7:136849018-136849068	HCF	heart:	n/a
33	chr7:136691229-136691279	HRE	kidney:	n/a
34	chr7:136766058-136766108	T-47D	breast:	n/a
35	chr7:136794953-136795003	PFSK-1	brain:	n/a
36	chr7:136794953-136795003	Hela-S3	cervix:	n/a
37	chr7:136845265-136845315	AG09309	skin:	n/a
38	chr7:136879401-136879451	MCF-7	breast:	n/a
39	chr7:136698566-136698616	Caco-2	colon:	n/a
40	chr7:136685094-136685144	HRE	kidney:	n/a
41	chr7:136768089-136768139	AG09309	skin:	n/a
42	chr7:136849262-136849312	HCPEpiC	choroid plexus:	n/a
43	chr7:136691229-136691279	T-47D	breast:	n/a
44	chr7:136849143-136849193	GM06990	blood:	n/a
45	chr7:136794953-136795003	Caco-2	colon:	n/a
46	chr7:136832262-136832312	HNPCEpiC	eye:	n/a
47	chr7:136849262-136849312	BE2_C	brain:	n/a
48	chr7:136849018-136849068	Hela-S3	cervix:	n/a
49	chr7:136849262-136849312	NHDF-neo	bronchial:	n/a
50	chr7:136701166-136701216	K562	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:136690250..136691872-chr7:136692985..136695263,2	K562	blood:
2	chr7:136853684..136854424-chr7:137022605..137023178,2	MCF-7	breast:
3	chr7:136638125..136641155-chr7:136643037..136646443,3	K562	blood:
4	chr7:136690250..136691872-chr7:136692985..136695263,2	K562	blood:
5	chr7:136854007..136854801-chr7:137137517..137138269,2	MCF-7	breast:
6	chr7:136853636..136854568-chr7:137022322..137023760,5	MCF-7	breast:
7	chr7:136692793..136695681-chr7:136698031..136700404,3	K562	blood:
8	chr7:136701167..136703847-chr7:136709955..136712489,2	K562	blood:
9	chr7:136853367..136854657-chr7:137138615..137139665,11	MCF-7	breast:
10	chr7:136853692..136854573-chr7:137276894..137277671,4	MCF-7	breast:
11	chr7:136692793..136695681-chr7:136698031..136699650,2	K562	blood:
12	chr7:136858672..136861163-chr7:136864097..136866322,2	K562	blood:
13	chr7:136872945..136874531-chr7:136887427..136890361,2	MCF-7	breast:
14	chr7:136733893..136735505-chr7:136735883..136738187,2	K562	blood:
15	chr7:136858672..136861163-chr7:136864097..136866322,2	K562	blood:
16	chr7:136872945..136874531-chr7:136887427..136890361,2	MCF-7	breast:
17	chr7:136889214..136890885-chr7:136891240..136892885,2	K562	blood:
18	chr7:136853835..136854630-chr7:137138677..137139572,6	MCF-7	breast:
19	chr7:136853682..136854530-chr7:137276883..137277639,5	MCF-7	breast:
20	chr7:136768600..136771525-chr7:136904072..136906566,2	K562	blood:
21	chr2:196521592..196522296-chr7:136849044..136849880,2	HCT-116	colon:
22	chr7:136758590..136760294-chr7:136763517..136766034,2	K562	blood:
23	chr7:136845496..136847194-chr7:136910849..136912754,2	MCF-7	breast:
24	chr7:136798840..136800832-chr7:136803946..136805637,2	K562	blood:
25	chr7:136889214..136890885-chr7:136891240..136892885,2	K562	blood:
26	chr7:136692793..136695681-chr7:136698031..136699650,2	K562	blood:
27	chr7:136798840..136800832-chr7:136803946..136805637,2	K562	blood:
28	chr7:136758590..136760294-chr7:136763517..136766034,2	K562	blood:
29	chr4:150815194..150816071-chr7:136849876..136850472,2	MCF-7	breast:
30	chr7:136733893..136735505-chr7:136735883..136738187,2	K562	blood:
31	chr7:136692793..136695681-chr7:136698031..136700404,3	K562	blood:
32	chr7:136638125..136641155-chr7:136643037..136646443,3	K562	blood:
33	chr7:136701167..136703847-chr7:136709955..136712489,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTN-2	chr7:136848868-136849020	ENSG00000234352.5
2	lnc-PTN-2	chr7:136717541-136717660	ENSG00000234352
3	lnc-AC015987.1-7	chr7:136699568-136699701	NONHSAT123566
4	lnc-PTN-2	chr7:136804504-136805046	ENSG00000234352.5
5	lnc-PTN-2	chr7:136717541-136717660	ENSG00000234352.5
6	lnc-PTN-2	chr7:136848868-136849017	NONHSAT123574
7	lnc-AC015987.1-7	chr7:136699568-136699651	NONHSAT123564
8	lnc-AKR1D1-7	chr7:136660672-136662240	ucscGeneNc_uc003vts_1
9	lnc-PTN-2	chr7:136866355-136866518	ENSG00000234352
10	lnc-AKR1D1-7	chr7:136653879-136654144	ucscGeneNc_uc003vts_1
11	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
12	lnc-PTN-2	chr7:136717541-136717660	ENSG00000234352.5
13	lnc-PTN-2	chr7:136716652-136716710	ENSG00000234352.5
14	lnc-PTN-4	chr7:136888720-136888959	NONHSAT123576
15	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
16	lnc-PTN-2	chr7:136717541-136717660	ENSG00000234352.2
17	lnc-PTN-7	chr7:136763157-136763358	NONHSAT123572
18	lnc-PTN-2	chr7:136848868-136849022	ENSG00000234352.5
19	lnc-AC015987.1-7	chr7:136699568-136699651	NONHSAT123565
20	lnc-PTN-2	chr7:136804506-136805046	NONHSAT123574
21	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352.2
22	lnc-PTN-2	chr7:136717541-136717660	ENSG00000234352.5
23	lnc-PTN-2	chr7:136716652-136716710	ENSG00000234352
24	lnc-PTN-2	chr7:136848868-136849088	ENSG00000234352
25	lnc-PTN-8	chr7:136762787-136763014	NONHSAT123571
26	lnc-PTN-2	chr7:136848868-136849017	ENSG00000234352.5
27	lnc-PTN-4	chr7:136889380-136889587	NONHSAT123576
28	lnc-PTN-2	chr7:136717541-136717660	ENSG00000234352
29	lnc-PTN-6	chr7:136765503-136765733	NONHSAT123573

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CHRM2	hsa-miR-335-5p	chr7:136701273-136701293

Variant related genes	Relation type
ENSG00000224469	TF binding region
ENSG00000234352	TF binding region
ENSG00000224469	CpG island
ENSG00000234352	CpG island
ENSG00000157680	chromatin interactions
ENSG00000196950	chromatin interactions
FBN1	miRNA target sites
SLC35B4	miRNA target sites
MUC17	miRNA target sites
RFC3	miRNA target sites

Extended variants
information (count: 7838 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:7838 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180944533	chr7:136633748-136633749	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557029852	chr7:136633752-136633753	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185114677	chr7:136633859-136633860	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200806866	chr7:136633900-136633901	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192320456	chr7:136633907-136633908	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75072377	chr7:136633928-136633929	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138998683	chr7:136633930-136633931	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184093224	chr7:136633970-136633971	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562442285	chr7:136633997-136633998	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370123005	chr7:136634009-136634010	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142982381	chr7:136634028-136634029	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187289437	chr7:136634072-136634073	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533061011	chr7:136634136-136634137	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191731454	chr7:136634140-136634141	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373010041	chr7:136634206-136634207	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs386411435	chr7:136634207-136634208	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386411436	chr7:136634223-136634224	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373501837	chr7:136634225-136634226	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs71533720	chr7:136634237-136634238	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566488178	chr7:136634327-136634328	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535464247	chr7:136634405-136634406	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548984178	chr7:136634473-136634474	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35575870	chr7:136634490-136634491	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78781054	chr7:136634491-136634492	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74764364	chr7:136634502-136634503	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201935314	chr7:136634503-136634504	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74934612	chr7:136634504-136634505	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569178477	chr7:136634513-136634514	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112144176	chr7:136634539-136634540	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147438276	chr7:136634549-136634550	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148479562	chr7:136634551-136634552	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539567563	chr7:136634556-136634557	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17168824	chr7:136634627-136634628	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs547261624	chr7:136634628-136634629	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75517010	chr7:136634701-136634702	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539467709	chr7:136634754-136634755	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142622553	chr7:136634761-136634762	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555784463	chr7:136634762-136634763	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575936151	chr7:136634777-136634778	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114710856	chr7:136634797-136634798	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575969360	chr7:136634870-136634871	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201469534	chr7:136634879-136634880	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564689284	chr7:136634938-136634939	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1378646	chr7:136635001-136635002	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs187094379	chr7:136635002-136635003	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150549905	chr7:136635012-136635013	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73727442	chr7:136635013-136635014	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs569015719	chr7:136635021-136635022	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373015789	chr7:136635060-136635061	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1378645	chr7:136635091-136635092	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

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
Adenocarcinoma	21044232	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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	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
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136607800-136638000	Weak transcription	NHLF	lung
2	chr7:136623400-136641600	Weak transcription	Right Ventricle	heart
3	chr7:136623600-136641600	Weak transcription	Left Ventricle	heart
4	chr7:136631600-136636400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:136631800-136635800	Weak transcription	Colon Smooth Muscle	Colon
6	chr7:136632600-136633800	Enhancers	Right Atrium	heart
7	chr7:136633400-136635000	Weak transcription	Fetal Heart	heart
8	chr7:136633600-136633800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:136633600-136633800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:136633800-136635800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:136633800-136641400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr7:136634000-136638400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:136635000-136637200	Enhancers	Fetal Heart	heart
14	chr7:136635600-136641400	Weak transcription	Stomach Smooth Muscle	stomach
15	chr7:136635800-136636200	Enhancers	Rectal Smooth Muscle	rectum
16	chr7:136635800-136637200	Enhancers	Colon Smooth Muscle	Colon
17	chr7:136636200-136638200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr7:136636400-136637000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:136637000-136638400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:136637200-136638200	Weak transcription	Colon Smooth Muscle	Colon
21	chr7:136637200-136639800	Weak transcription	Fetal Heart	heart
22	chr7:136638000-136638800	Enhancers	NH-A	brain
23	chr7:136638000-136638800	Enhancers	Osteobl	bone
24	chr7:136638000-136639000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr7:136638000-136639000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:136638000-136639000	Enhancers	NHLF	lung
27	chr7:136638000-136641200	Enhancers	HUVEC	blood vessel
28	chr7:136638200-136638800	Enhancers	Rectal Smooth Muscle	rectum
29	chr7:136638200-136639000	Enhancers	Colon Smooth Muscle	Colon
30	chr7:136638400-136638600	Weak transcription	Gastric	stomach
31	chr7:136638400-136638800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:136638400-136638800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:136638400-136638800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr7:136638400-136640400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:136638400-136640600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:136638400-136642200	Enhancers	Placenta Amnion	Placenta Amnion
37	chr7:136638600-136638800	Enhancers	Gastric	stomach
38	chr7:136638600-136638800	Enhancers	Lung	lung
39	chr7:136638800-136640200	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr7:136638800-136640200	Weak transcription	NH-A	brain
41	chr7:136638800-136640200	Weak transcription	Osteobl	bone
42	chr7:136638800-136641600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:136638800-136641600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:136638800-136641600	Weak transcription	Gastric	stomach
45	chr7:136638800-136641600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr7:136639000-136640000	Weak transcription	NHLF	lung
47	chr7:136639000-136640200	Weak transcription	Colon Smooth Muscle	Colon
48	chr7:136639000-136640400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:136639000-136641400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:136639400-136641600	Weak transcription	Pancreas	Pancrea

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