Variant report

Variant	nsv831066
Chromosome Location	chr7:97726879-97890550
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4024)
CpG islands
(count:6595)
Chromatin interactive
region (count:178)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4024 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97746162-97746900	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:97855510-97855782	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:97797949-97798179	K562	blood:	n/a	n/a
4	ARID3A	chr7:97884715-97884806	K562	blood:	n/a	n/a
5	ARID3A	chr7:97761182-97761188	K562	blood:	n/a	n/a
6	ARID3A	chr7:97762101-97763279	K562	blood:	n/a	n/a
7	ARID3A	chr7:97841106-97841413	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:97847663-97847944	K562	blood:	n/a	n/a
9	ARID3A	chr7:97739788-97740472	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:97760693-97761553	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:97881427-97882096	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:97748571-97748761	HepG2	liver:	n/a	chr7:97748648-97748664
13	ARID3A	chr7:97762912-97763551	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:97735778-97736205	K562	blood:	n/a	n/a
15	ARID3A	chr7:97735655-97736271	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:97776066-97776266	K562	blood:	n/a	n/a
17	ARID3A	chr7:97755970-97756278	HepG2	liver:	n/a	n/a
18	ARID3A	chr7:97762179-97762699	HepG2	liver:	n/a	n/a
19	ARID3A	chr7:97737548-97738113	HepG2	liver:	n/a	n/a
20	ATF1	chr7:97813478-97813676	K562	blood:	n/a	n/a
21	ATF1	chr7:97739909-97740207	K562	blood:	n/a	n/a
22	ATF1	chr7:97761152-97761556	K562	blood:	n/a	n/a
23	ATF1	chr7:97881467-97881729	K562	blood:	n/a	n/a
24	ATF1	chr7:97762395-97762803	K562	blood:	n/a	n/a
25	ATF1	chr7:97884669-97884833	K562	blood:	n/a	n/a
26	ATF1	chr7:97804622-97804945	K562	blood:	n/a	n/a
27	ATF1	chr7:97735552-97736368	K562	blood:	n/a	n/a
28	ATF2	chr7:97766964-97767432	GM12878	blood:	n/a	n/a
29	ATF2	chr7:97766781-97767513	GM12878	blood:	n/a	n/a
30	ATF2	chr7:97848596-97849007	GM12878	blood:	n/a	n/a
31	ATF2	chr7:97735798-97736331	GM12878	blood:	n/a	n/a
32	ATF2	chr7:97849099-97849509	GM12878	blood:	n/a	n/a
33	ATF2	chr7:97831540-97832306	GM12878	blood:	n/a	n/a
34	ATF2	chr7:97829493-97830274	GM12878	blood:	n/a	n/a
35	ATF2	chr7:97832597-97832988	GM12878	blood:	n/a	n/a
36	ATF2	chr7:97831639-97832231	GM12878	blood:	n/a	n/a
37	ATF2	chr7:97762407-97762925	GM12878	blood:	n/a	n/a
38	ATF2	chr7:97735853-97736328	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr7:97735863-97736282	GM12878	blood:	n/a	n/a
40	ATF2	chr7:97762353-97762978	GM12878	blood:	n/a	n/a
41	ATF2	chr7:97832563-97833050	GM12878	blood:	n/a	n/a
42	ATF3	chr7:97735969-97736249	H1-hESC	embryonic stem cell:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
43	ATF3	chr7:97797843-97798226	K562	blood:	n/a	n/a
44	ATF3	chr7:97735906-97736370	GM12878	blood:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
45	ATF3	chr7:97735997-97736461	A549	lung:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
46	ATF3	chr7:97735965-97736320	K562	blood:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
47	ATF3	chr7:97735985-97736348	HepG2	liver:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
48	ATF3	chr7:97736082-97736271	GM12878	blood:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
49	ATF3	chr7:97841200-97841340	K562	blood:	n/a	n/a
50	ATF3	chr7:97735940-97736387	H1-hESC	embryonic stem cell:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193

(count:6595 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97833388-97833438	PFSK-1	brain:	n/a
2	chr7:97882260-97882310	HEK293	kidney:	embryo
3	chr7:97838659-97838709	NHDF-neo	bronchial:	n/a
4	chr7:97842268-97842318	HIPEpiC	eye:	n/a
5	chr7:97823438-97823488	AG04449	skin:	fetal
6	chr7:97836563-97836613	HCF	heart:	n/a
7	chr7:97736378-97736428	PrEC	prostate:	n/a
8	chr7:97833388-97833438	PFSK-1	brain:	n/a
9	chr7:97882260-97882310	HEK293	kidney:	embryo
10	chr7:97838659-97838709	NHDF-neo	bronchial:	n/a
11	chr7:97842268-97842318	HIPEpiC	eye:	n/a
12	chr7:97823438-97823488	AG04449	skin:	fetal
13	chr7:97836563-97836613	HCF	heart:	n/a
14	chr7:97736378-97736428	PrEC	prostate:	n/a
15	chr7:97821646-97821696	HRPEpiC	eye:	n/a
16	chr7:97821546-97821596	HUVEC	blood vessel:	n/a
17	chr7:97804838-97804888	PrEC	prostate:	n/a
18	chr7:97823410-97823460	PFSK-1	brain:	n/a
19	chr7:97857989-97858039	HCM	heart:	n/a
20	chr7:97834623-97834673	HMEC	breast:	n/a
21	chr7:97846988-97847038	HCM	heart:	n/a
22	chr7:97868109-97868159	AoSMC	blood vessel:	n/a
23	chr7:97800895-97800945	GM12891	blood:	n/a
24	chr7:97821037-97821087	AG04450	lung:	fetal
25	chr7:97884367-97884417	A549	lung:	n/a
26	chr7:97880848-97880898	PFSK-1	brain:	n/a
27	chr7:97739696-97739746	RPTEC	kidney:	n/a
28	chr7:97841502-97841552	HAEpiC	amniotic membrane:	n/a
29	chr7:97821499-97821549	NB4	blood:	n/a
30	chr7:97851854-97851904	BE2_C	brain:	n/a
31	chr7:97882137-97882187	ProgFib	skin:	n/a
32	chr7:97807699-97807749	HUVEC	blood vessel:	n/a
33	chr7:97857647-97857697	GM12892	blood:	n/a
34	chr7:97841334-97841384	K562	blood:	n/a
35	chr7:97881573-97881623	HRCEpiC	kidney:	n/a
36	chr7:97833154-97833204	HRPEpiC	eye:	n/a
37	chr7:97822857-97822907	AoSMC	blood vessel:	n/a
38	chr7:97852022-97852072	SAEC	small airway:	n/a
39	chr7:97841513-97841563	Hepatocyte	liver:	n/a
40	chr7:97841998-97842048	NHDF-neo	bronchial:	n/a
41	chr7:97881723-97881773	NT2-D1	testis:	n/a
42	chr7:97841864-97841914	MCF10A-Er-Src	breast:	n/a
43	chr7:97835192-97835242	AG04449	skin:	fetal
44	chr7:97801494-97801544	GM12892	blood:	n/a
45	chr7:97841998-97842048	NB4	blood:	n/a
46	chr7:97807643-97807693	GM12878	blood:	n/a
47	chr7:97800932-97800982	HIPEpiC	eye:	n/a
48	chr7:97882137-97882187	NH-A	brain:	n/a
49	chr7:97807699-97807749	NHBE	bronchial:	n/a
50	chr7:97736138-97736188	AG04450	lung:	fetal

(count:178 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:97781216..97783623-chr7:97806937..97808476,2	K562	blood:
2	chr7:97806745..97809009-chr7:97810753..97812521,2	K562	blood:
3	chr7:97737313..97739536-chr7:97747241..97749393,2	K562	blood:
4	chr7:97765887..97768071-chr7:97777443..97779384,2	MCF-7	breast:
5	chr7:97848875..97850795-chr7:97850910..97852902,2	K562	blood:
6	chr7:97738785..97741480-chr7:97751864..97754009,2	MCF-7	breast:
7	chr7:97751191..97752797-chr7:97754258..97756378,2	MCF-7	breast:
8	chr7:97881770..97884305-chr7:97885648..97888001,2	K562	blood:
9	chr7:97840601..97843525-chr7:97854047..97856792,2	MCF-7	breast:
10	chr7:97840856..97842377-chr7:97845637..97848224,2	MCF-7	breast:
11	chr7:97753385..97755585-chr7:97757757..97760678,3	K562	blood:
12	chr7:97801945..97806257-chr7:97807779..97810012,4	K562	blood:
13	chr7:97787814..97789772-chr7:97791387..97793183,2	MCF-7	breast:
14	chr7:97735258..97737646-chr7:97747785..97750539,2	MCF-7	breast:
15	chr7:97847018..97848537-chr7:97878984..97881844,2	K562	blood:
16	chr7:97840173..97842487-chr7:97845725..97848039,2	MCF-7	breast:
17	chr7:97785345..97788078-chr7:97789745..97792184,3	K562	blood:
18	chr7:97844457..97846470-chr7:97865336..97867376,2	MCF-7	breast:
19	chr7:97839660..97842920-chr7:97872632..97874833,3	K562	blood:
20	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
21	chr7:97756277..97758214-chr7:97760043..97763827,4	MCF-7	breast:
22	chr7:97737661..97739310-chr7:97740344..97742596,2	MCF-7	breast:
23	chr7:97782886..97785109-chr7:97786892..97788844,2	K562	blood:
24	chr7:97781216..97783623-chr7:97806937..97808476,2	K562	blood:
25	chr7:97797557..97798288-chr7:97870683..97871212,2	MCF-7	breast:
26	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
27	chr7:97789932..97791977-chr7:97793764..97795356,2	K562	blood:
28	chr7:97768037..97770544-chr7:97772869..97774678,2	K562	blood:
29	chr7:97735682..97736214-chr7:97870411..97871232,2	K562	blood:
30	chr7:97803390..97805709-chr7:97805950..97808226,2	MCF-7	breast:
31	chr20:48807269..48810011-chr7:97735604..97737144,2	MCF-7	breast:
32	chr10:8099641..8101523-chr7:97840811..97843007,2	MCF-7	breast:
33	chr7:97859627..97861679-chr7:97864267..97867211,3	K562	blood:
34	chr7:97729021..97732644-chr7:97733894..97737983,4	MCF-7	breast:
35	chr7:97829526..97831904-chr7:97833458..97836322,3	K562	blood:
36	chr7:97843013..97845825-chr7:97853837..97855430,2	MCF-7	breast:
37	chr7:97753385..97755585-chr7:97757757..97760678,3	K562	blood:
38	chr7:97762740..97765611-chr7:97766215..97769576,3	K562	blood:
39	chr7:97789932..97791977-chr7:97793764..97795356,2	K562	blood:
40	chr7:97739559..97743131-chr7:97746340..97751154,6	MCF-7	breast:
41	chr7:97846624..97850033-chr7:97850682..97852457,3	MCF-7	breast:
42	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
43	chr7:97725965..97727717-chr7:97803967..97806554,2	K562	blood:
44	chr7:97850503..97852580-chr7:97856044..97857561,2	MCF-7	breast:
45	chr7:97806745..97809702-chr7:97810753..97813154,2	K562	blood:
46	chr7:97829526..97831904-chr7:97833458..97836322,3	K562	blood:
47	chr7:97735652..97737286-chr7:97753750..97756683,2	MCF-7	breast:
48	chr7:97734947..97737685-chr7:97796527..97798334,3	K562	blood:
49	chr7:97859339..97861738-chr7:97869663..97872291,2	MCF-7	breast:
50	chr7:97735853..97738085-chr7:97746121..97749731,3	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAIAP2L1.1-1	chr7:97881438-97881487	NONHSAT122185
2	lnc-BHLHA15-1	chr7:97841568-97841603	NONHSAT122177
3	lnc-TECPR1-2	chr7:97752600-97755814	NONHSAT122171
4	lnc-BRI3-2	chr7:97882196-97882353	NONHSAT122187
5	lnc-BAIAP2L1.1-1	chr7:97880226-97880860	NONHSAT122185
6	lnc-BRI3-2	chr7:97881470-97887682	NONHSAT122186
7	lnc-BHLHA15-1	chr7:97840778-97840810	NONHSAT122177
8	lnc-BAIAP2L1.1-1	chr7:97881438-97881468	NONHSAT122183
9	lnc-BRI3-2	chr7:97881586-97882094	NONHSAT122187
10	lnc-BAIAP2L1.1-1	chr7:97880731-97880860	NONHSAT122183
11	lnc-BHLHA15-1	chr7:97842411-97844754	NONHSAT122177
12	lnc-BAIAP2L1.1-1	chr7:97855904-97856081	NONHSAT122183

No data

Variant related genes	Relation type
BHLHA15	TF binding region
LMTK2	TF binding region
TECPR1	TF binding region
BRI3	TF binding region
BHLHA15	CpG island
LMTK2	CpG island
TECPR1	CpG island
BRI3	CpG island
ENSG00000243554	chromatin interactions
ENSG00000164713	chromatin interactions
ENSG00000006453	chromatin interactions
ENSG00000164715	chromatin interactions
ENSG00000107485	chromatin interactions
ENSG00000179218	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000180535	chromatin interactions
ENSG00000172216	chromatin interactions
ENSG00000099622	chromatin interactions

Extended variants
information (count: 6967 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6967 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115919732	chr7:97726885-97726886	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs528143039	chr7:97726886-97726887	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147417497	chr7:97726917-97726918	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546293100	chr7:97726996-97726997	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543413135	chr7:97727039-97727040	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568082090	chr7:97727106-97727107	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139643547	chr7:97727116-97727117	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555691088	chr7:97727123-97727124	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs77407257	chr7:97727208-97727209	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562818157	chr7:97727364-97727365	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544765735	chr7:97727396-97727397	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs181422279	chr7:97727407-97727408	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184489487	chr7:97727426-97727427	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2172883	chr7:97727429-97727430	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529921143	chr7:97727465-97727466	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs6980318	chr7:97727480-97727481	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566367624	chr7:97727540-97727541	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561084462	chr7:97727597-97727598	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115115822	chr7:97727630-97727631	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543744843	chr7:97727784-97727785	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527477985	chr7:97727788-97727789	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189202210	chr7:97727816-97727817	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551106892	chr7:97727833-97727834	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs35476396	chr7:97727843-97727844	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532580013	chr7:97727910-97727911	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547558323	chr7:97727938-97727939	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566137684	chr7:97727944-97727945	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs117755755	chr7:97728015-97728016	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375435750	chr7:97728044-97728045	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548333634	chr7:97728045-97728046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs117070905	chr7:97728087-97728088	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs141807038	chr7:97728094-97728095	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs559241698	chr7:97728121-97728122	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571138463	chr7:97728174-97728175	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376218765	chr7:97728176-97728177	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553512696	chr7:97728190-97728191	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370262002	chr7:97728221-97728222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77243012	chr7:97728260-97728261	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs555857351	chr7:97728288-97728289	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568025895	chr7:97728358-97728359	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554759952	chr7:97728392-97728393	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576352937	chr7:97728415-97728416	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181845663	chr7:97728420-97728421	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs79354079	chr7:97728441-97728442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs34307903	chr7:97728449-97728450	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs541382332	chr7:97728520-97728521	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559044040	chr7:97728537-97728538	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs200007454	chr7:97728612-97728613	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs201224434	chr7:97728613-97728614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567417494	chr7:97728615-97728616	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:6273 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97726600-97727200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:97733200-97734600	Enhancers	HepG2	liver
3	chr7:97733600-97736000	Weak transcription	Right Atrium	heart
4	chr7:97734000-97736000	Enhancers	Fetal Intestine Small	intestine
5	chr7:97734600-97736000	Flanking Active TSS	HepG2	liver
6	chr7:97735200-97735400	Enhancers	Duodenum Mucosa	Duodenum
7	chr7:97735200-97735400	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr7:97735200-97735400	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr7:97735200-97735400	Enhancers	Hela-S3	cervix
10	chr7:97735200-97735600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:97735200-97735600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:97735200-97735800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr7:97735200-97736000	Enhancers	Primary T cells from cord blood	blood
14	chr7:97735200-97736000	Enhancers	Fetal Intestine Large	intestine
15	chr7:97735400-97735600	Enhancers	Brain Angular Gyrus	brain
16	chr7:97735400-97735600	Enhancers	Brain Anterior Caudate	brain
17	chr7:97735400-97735600	Enhancers	Brain Cingulate Gyrus	brain
18	chr7:97735400-97735600	Enhancers	Brain Hippocampus Middle	brain
19	chr7:97735400-97735600	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr7:97735400-97735600	Flanking Active TSS	Esophagus	oesophagus
21	chr7:97735400-97735600	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr7:97735400-97735600	Enhancers	Dnd41	blood
23	chr7:97735400-97735600	Active TSS	NHEK	skin
24	chr7:97735400-97735800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:97735400-97735800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
26	chr7:97735400-97735800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr7:97735400-97735800	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr7:97735400-97735800	Enhancers	Right Ventricle	heart
29	chr7:97735400-97735800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr7:97735400-97735800	Enhancers	HMEC	breast
31	chr7:97735400-97736000	Enhancers	Primary B cells from peripheral blood	blood
32	chr7:97735400-97736000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr7:97735400-97736000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr7:97735400-97736000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr7:97735400-97736000	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr7:97735400-97736000	Enhancers	Pancreas	Pancrea
37	chr7:97735400-97736000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
38	chr7:97735400-97736000	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr7:97735400-97736000	Flanking Active TSS	Hela-S3	cervix
40	chr7:97735400-97736200	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr7:97735400-97737400	Active TSS	Stomach Smooth Muscle	stomach
42	chr7:97735600-97735800	Flanking Active TSS	Brain Angular Gyrus	brain
43	chr7:97735600-97735800	Flanking Active TSS	Brain Hippocampus Middle	brain
44	chr7:97735600-97735800	Enhancers	Esophagus	oesophagus
45	chr7:97735600-97735800	Enhancers	Fetal Heart	heart
46	chr7:97735600-97735800	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr7:97735600-97735800	Enhancers	Placenta	Placenta
48	chr7:97735600-97735800	Enhancers	Fetal Thymus	thymus
49	chr7:97735600-97735800	Enhancers	K562	blood
50	chr7:97735600-97736000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast

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