Variant report

Variant	esv2756451
Chromosome Location	chr7:110981267-111199127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1841)
CpG islands
(count:244)
Chromatin interactive
region (count:191)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1841 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
3	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
4	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
5	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
6	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
8	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
9	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
12	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
13	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
14	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
15	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
17	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
18	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
19	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
20	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
21	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
22	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
23	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
24	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
25	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
26	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
27	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
28	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
29	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
31	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
32	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
33	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
34	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a
35	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
36	ATF3	chr7:111156586-111157138	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
37	ATF3	chr7:111156585-111157142	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
38	BACH1	chr7:111172186-111172416	K562	blood:	n/a	n/a
39	BACH1	chr7:111188905-111189076	K562	blood:	n/a	n/a
40	BACH1	chr7:111169257-111169277	K562	blood:	n/a	n/a
41	BACH1	chr7:111160755-111160869	K562	blood:	n/a	n/a
42	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
43	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:111168484-111168730	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
46	BCL3	chr7:111138913-111139703	A549	lung:	n/a	chr7:111138981-111138990
47	BCL3	chr7:111156319-111157358	A549	lung:	n/a	n/a
48	BCL3	chr7:111156597-111157052	A549	lung:	n/a	n/a
49	BCL3	chr7:111139024-111139659	A549	lung:	n/a	n/a
50	BCLAF1	chr7:111168247-111168782	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111033064-111033114	HCF	heart:	n/a
2	chr7:111198163-111198213	AG09309	skin:	n/a
3	chr7:111079100-111079150	SK-N-SH	brain:	n/a
4	chr7:111198163-111198213	ProgFib	skin:	n/a
5	chr7:111086055-111086105	GM12892	blood:	n/a
6	chr7:111033064-111033114	GM19239	blood:	n/a
7	chr7:111086055-111086105	AG09309	skin:	n/a
8	chr7:111079100-111079150	AG09319	gingival:	n/a
9	chr7:111198163-111198213	SK-N-SH	brain:	n/a
10	chr7:111033064-111033114	IMR90	lung:	fetal
11	chr7:111198163-111198213	AG04449	skin:	fetal
12	chr7:111086055-111086105	SKMC	muscle:	n/a
13	chr7:111086055-111086105	HAEpiC	amniotic membrane:	n/a
14	chr7:111086055-111086105	A549	lung:	n/a
15	chr7:111198163-111198213	U87	brain:	n/a
16	chr7:111198163-111198213	Caco-2	colon:	n/a
17	chr7:111033064-111033114	NT2-D1	testis:	n/a
18	chr7:111198163-111198213	HMEC	breast:	n/a
19	chr7:111198163-111198213	HNPCEpiC	eye:	n/a
20	chr7:111079100-111079150	NH-A	brain:	n/a
21	chr7:111079100-111079150	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:111033064-111033114	NH-A	brain:	n/a
23	chr7:111079100-111079150	AG04450	lung:	fetal
24	chr7:111079100-111079150	PFSK-1	brain:	n/a
25	chr7:111079100-111079150	GM19239	blood:	n/a
26	chr7:111079100-111079150	HRPEpiC	eye:	n/a
27	chr7:111033064-111033114	PrEC	prostate:	n/a
28	chr7:111033064-111033114	GM12891	blood:	n/a
29	chr7:111198163-111198213	IMR90	lung:	fetal
30	chr7:111086055-111086105	ECC-1	luminal epithelium:	n/a
31	chr7:111079100-111079150	HEK293	kidney:	embryo
32	chr7:111033064-111033114	ECC-1	luminal epithelium:	n/a
33	chr7:111079100-111079150	Caco-2	colon:	n/a
34	chr7:111033064-111033114	NHDF-neo	bronchial:	n/a
35	chr7:111198163-111198213	ovcar-3	ovarian:	n/a
36	chr7:111198163-111198213	HIPEpiC	eye:	n/a
37	chr7:111086055-111086105	GM12891	blood:	n/a
38	chr7:111033064-111033114	LNCaP	prostate:	n/a
39	chr7:111086055-111086105	AG10803	skin:	n/a
40	chr7:111198163-111198213	GM12878	blood:	n/a
41	chr7:111079100-111079150	BJ	skin:	n/a
42	chr7:111086055-111086105	HIPEpiC	eye:	n/a
43	chr7:111198163-111198213	HEK293	kidney:	embryo
44	chr7:111079100-111079150	U87	brain:	n/a
45	chr7:111079100-111079150	LNCaP	prostate:	n/a
46	chr7:111086055-111086105	HUVEC	blood vessel:	n/a
47	chr7:111079100-111079150	HEEpiC	esophagus:	n/a
48	chr7:111079100-111079150	HCPEpiC	choroid plexus:	n/a
49	chr7:111033064-111033114	GM12892	blood:	n/a
50	chr7:111079100-111079150	AG04449	skin:	fetal

(count:191 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:111154283..111157202-chr7:111157997..111159947,2	MCF-7	breast:
2	chr7:111154605..111156613-chr7:111179034..111181673,2	K562	blood:
3	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
4	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
5	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
6	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
7	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
8	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
9	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
10	chr7:111165046..111169719-chr7:111171827..111173771,4	K562	blood:
11	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
12	chr7:111178053..111179952-chr7:111201249..111203327,2	MCF-7	breast:
13	chr7:111164432..111166766-chr7:111167043..111169484,2	MCF-7	breast:
14	chr7:111165046..111169719-chr7:111171827..111173771,4	K562	blood:
15	chr7:111162292..111164581-chr7:111182567..111185234,2	K562	blood:
16	chr12:108200986..108203742-chr7:111052172..111055145,3	MCF-7	breast:
17	chr7:111149350..111150943-chr7:111156315..111157965,2	K562	blood:
18	chr7:111067248..111069567-chr7:111070405..111074153,3	K562	blood:
19	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
20	chr7:111165046..111167501-chr7:111171827..111173680,2	K562	blood:
21	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
22	chr7:111198013..111199792-chr7:111239009..111241221,2	K562	blood:
23	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
24	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
25	chr7:111100148..111100705-chr7:111129526..111130134,2	K562	blood:
26	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
27	chr7:111164175..111171930-chr7:111196711..111203728,11	K562	blood:
28	chr7:111182436..111184713-chr7:111201121..111202847,2	MCF-7	breast:
29	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
30	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
31	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
32	chr7:111118102..111121485-chr7:111125299..111129711,6	K562	blood:
33	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
34	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
35	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
36	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
37	chr1:231114585..231115155-chr7:111179137..111179637,2	NB4	blood:
38	chr7:110975357..110976070-chr7:111125914..111126817,2	K562	blood:
39	chr7:111020866..111024340-chr7:111025481..111028509,4	MCF-7	breast:
40	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
41	chr7:110978869..110982048-chr7:110982767..110985792,3	K562	blood:
42	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
43	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:
44	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
45	chr7:111150770..111153588-chr7:111154725..111157322,3	K562	blood:
46	chr7:111126340..111126902-chr7:111381753..111382269,2	K562	blood:
47	chr7:111183053..111185306-chr7:111210487..111212870,2	K562	blood:
48	chr7:111050112..111052168-chr7:111053965..111056674,3	K562	blood:
49	chr7:111164979..111167158-chr7:111168899..111171034,2	MCF-7	breast:
50	chr7:111172393..111173981-chr7:111189118..111191154,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
IMMP2L	TF binding region
ENSG00000243621	TF binding region
ENSG00000227948	CpG island
IMMP2L	CpG island
ENSG00000243621	CpG island
ENSG00000143643	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000173409	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000204463	chromatin interactions

Extended variants
information (count: 7811 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7811 , 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	rs11978401	chr7:110981267-110981268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568932746	chr7:110981287-110981288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538954848	chr7:110981322-110981323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545990655	chr7:110981344-110981345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80003296	chr7:110981361-110981362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187886170	chr7:110981363-110981364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533882354	chr7:110981445-110981446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138722521	chr7:110981465-110981466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570520924	chr7:110981497-110981498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116214185	chr7:110981510-110981511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192407909	chr7:110981524-110981525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184534888	chr7:110981530-110981531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187718434	chr7:110981548-110981549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554097762	chr7:110981564-110981565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376943993	chr7:110981685-110981686	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs572770864	chr7:110981691-110981692	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs546558208	chr7:110981703-110981704	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs564825164	chr7:110981719-110981720	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs118030735	chr7:110981740-110981741	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs552298940	chr7:110981828-110981829	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs543939699	chr7:110981874-110981875	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs562590494	chr7:110981975-110981976	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs564649525	chr7:110982051-110982052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13227788	chr7:110982052-110982053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531293665	chr7:110982055-110982056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544280194	chr7:110982066-110982067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527542815	chr7:110982084-110982085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6956410	chr7:110982095-110982096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570484433	chr7:110982108-110982109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371441653	chr7:110982156-110982157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538253898	chr7:110982201-110982202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560977082	chr7:110982253-110982254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373840896	chr7:110982255-110982256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568517344	chr7:110982289-110982290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551951109	chr7:110982330-110982331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs37644	chr7:110982360-110982361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs569476954	chr7:110982387-110982388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6978694	chr7:110982401-110982402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572684671	chr7:110982404-110982405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546494981	chr7:110982416-110982417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113895131	chr7:110982443-110982444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112499454	chr7:110982446-110982447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs11983744	chr7:110982459-110982460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs377675998	chr7:110982473-110982474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536933956	chr7:110982474-110982475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544175196	chr7:110982508-110982509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562392436	chr7:110982509-110982510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528640822	chr7:110982519-110982520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs37645	chr7:110982545-110982546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs146254219	chr7:110982570-110982571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1439 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110960000-110983400	Weak transcription	Left Ventricle	heart
2	chr7:110973800-110983400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:110979400-110981600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:110980800-110983200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr7:110981600-110982000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:110983200-110983600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr7:110983400-110983600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:110983400-110983600	ZNF genes & repeats	Left Ventricle	heart
9	chr7:110983400-110983800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
10	chr7:110983600-110984200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:110984000-110985600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:110987000-110987800	Enhancers	Psoas Muscle	Psoas
13	chr7:110987400-111002800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:110987800-110989600	Weak transcription	Psoas Muscle	Psoas
15	chr7:110989600-110989800	Enhancers	Psoas Muscle	Psoas
16	chr7:110996800-110997400	Enhancers	K562	blood
17	chr7:110997000-110997200	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr7:110997000-110997200	Enhancers	HSMMtube	muscle
19	chr7:110997000-110997800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:110997000-110998200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr7:110997000-110998400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:110997000-110998600	Enhancers	A549	lung
23	chr7:110997000-110998800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:110997000-110999000	Enhancers	HMEC	breast
25	chr7:110997000-110999200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:110997000-110999200	Enhancers	Hela-S3	cervix
27	chr7:110997000-110999400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:110997000-110999800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr7:110997200-110997400	Enhancers	NH-A	brain
30	chr7:110997200-110998000	Weak transcription	HSMMtube	muscle
31	chr7:110997200-110998200	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr7:110997200-110998200	Enhancers	Osteobl	bone
33	chr7:110997200-110998400	Enhancers	HSMM	muscle
34	chr7:110997200-110998600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:110997200-110999200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:110997400-110998000	Enhancers	NHEK	skin
37	chr7:110997400-110998400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:110997400-110998400	Enhancers	NHDF-Ad	bronchial
39	chr7:110997400-111002800	Weak transcription	NH-A	brain
40	chr7:110997400-111008200	Weak transcription	K562	blood
41	chr7:110997600-110998400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:110997800-110998400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:110997800-111002600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr7:110998000-110998400	Enhancers	HSMMtube	muscle
45	chr7:110998000-110998400	Flanking Active TSS	NHEK	skin
46	chr7:110998000-110999200	Enhancers	Right Atrium	heart
47	chr7:110998000-110999400	Enhancers	Aorta	Aorta
48	chr7:110998200-110998600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:110998200-110998600	Enhancers	Stomach Mucosa	stomach
50	chr7:110998200-110999200	Enhancers	Skeletal Muscle Female	skeletal muscle

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