Variant report

Variant	esv2422497
Chromosome Location	chr7:110821726-111158074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2589)
CpG islands
(count:366)
Chromatin interactive
region (count:257)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2589 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
2	ARID3A	chr7:110830821-110831569	K562	blood:	n/a	n/a
3	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
4	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
5	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
8	ARID3A	chr7:110869353-110869485	K562	blood:	n/a	n/a
9	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
10	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
11	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
12	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
13	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
14	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
15	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
16	ARID3A	chr7:110832610-110833023	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
18	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
19	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
20	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
21	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
22	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
23	ARID3A	chr7:110863537-110864343	K562	blood:	n/a	chr7:110863547-110863563 chr7:110863548-110863564
24	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
25	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
26	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
27	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
28	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
29	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
30	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
31	ATF1	chr7:110889894-110890092	K562	blood:	n/a	n/a
32	ATF1	chr7:110863987-110864363	K562	blood:	n/a	n/a
33	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
34	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
35	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
36	ATF1	chr7:110830910-110831249	K562	blood:	n/a	n/a
37	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
38	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
39	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
40	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
41	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
42	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
43	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
44	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
45	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a
46	ATF3	chr7:110872430-110873085	A549	lung:	n/a	n/a
47	ATF3	chr7:110838322-110838906	HCT-116	colon:	n/a	n/a
48	BACH1	chr7:110935269-110935465	K562	blood:	n/a	n/a
49	BACH1	chr7:110864793-110865013	K562	blood:	n/a	n/a
50	BATF	chr7:110872545-110872818	GM12878	blood:	n/a	chr7:110872713-110872724 chr7:110872714-110872724

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111086055-111086105	PFSK-1	brain:	n/a
2	chr7:110906785-110906835	HNPCEpiC	eye:	n/a
3	chr7:111079100-111079150	BJ	skin:	n/a
4	chr7:111079100-111079150	T-47D	breast:	n/a
5	chr7:110879415-110879465	RPTEC	kidney:	n/a
6	chr7:110879415-110879465	SKMC	muscle:	n/a
7	chr7:110838461-110838511	AoSMC	blood vessel:	n/a
8	chr7:111033064-111033114	GM12891	blood:	n/a
9	chr7:111033064-111033114	GM19239	blood:	n/a
10	chr7:110879415-110879465	HRCEpiC	kidney:	n/a
11	chr7:111033064-111033114	K562	blood:	n/a
12	chr7:110838461-110838511	HMEC	breast:	n/a
13	chr7:110879415-110879465	HAEpiC	amniotic membrane:	n/a
14	chr7:111033064-111033114	LNCaP	prostate:	n/a
15	chr7:110906785-110906835	HAEpiC	amniotic membrane:	n/a
16	chr7:111086055-111086105	HCM	heart:	n/a
17	chr7:111033064-111033114	HEK293	kidney:	embryo
18	chr7:110879415-110879465	ProgFib	skin:	n/a
19	chr7:110879415-110879465	HCF	heart:	n/a
20	chr7:110838461-110838511	AG09319	gingival:	n/a
21	chr7:110838461-110838511	NHBE	bronchial:	n/a
22	chr7:111079100-111079150	NHBE	bronchial:	n/a
23	chr7:111079100-111079150	AG04449	skin:	fetal
24	chr7:111033064-111033114	HMEC	breast:	n/a
25	chr7:110838461-110838511	Caco-2	colon:	n/a
26	chr7:110879415-110879465	HMEC	breast:	n/a
27	chr7:111079100-111079150	AG04450	lung:	fetal
28	chr7:110906785-110906835	NHBE	bronchial:	n/a
29	chr7:110838461-110838511	HCF	heart:	n/a
30	chr7:111079100-111079150	HCPEpiC	choroid plexus:	n/a
31	chr7:111079100-111079150	HNPCEpiC	eye:	n/a
32	chr7:111033064-111033114	SKMC	muscle:	n/a
33	chr7:110879415-110879465	MCF10A-Er-Src	breast:	n/a
34	chr7:110879415-110879465	LNCaP	prostate:	n/a
35	chr7:111033064-111033114	T-47D	breast:	n/a
36	chr7:110879415-110879465	HL-60	blood:	n/a
37	chr7:110906785-110906835	T-47D	breast:	n/a
38	chr7:110838461-110838511	GM19239	blood:	n/a
39	chr7:110879415-110879465	NB4	blood:	n/a
40	chr7:110879415-110879465	GM12892	blood:	n/a
41	chr7:110906785-110906835	GM12878	blood:	n/a
42	chr7:110838461-110838511	SKMC	muscle:	n/a
43	chr7:111033064-111033114	CMK	blood:	n/a
44	chr7:111079100-111079150	PFSK-1	brain:	n/a
45	chr7:110838461-110838511	NH-A	brain:	n/a
46	chr7:110879415-110879465	BJ	skin:	n/a
47	chr7:111033064-111033114	AG09309	skin:	n/a
48	chr7:110906785-110906835	AG10803	skin:	n/a
49	chr7:110838461-110838511	HRE	kidney:	n/a
50	chr7:111086055-111086105	SK-N-MC	brain:	n/a

(count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:110901427..110902958-chr7:110904579..110907166,2	MCF-7	breast:
2	chr7:110867615..110869914-chr7:110870998..110874841,5	K562	blood:
3	chr7:110890356..110892390-chr7:110893967..110896589,2	K562	blood:
4	chr7:110822071..110825302-chr7:110827142..110830150,3	K562	blood:
5	chr7:111043409..111046006-chr7:111053282..111056029,3	K562	blood:
6	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
7	chr7:110836787..110838968-chr7:110842164..110843669,2	K562	blood:
8	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
9	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
10	chr7:111098758..111101723-chr7:111103712..111106818,3	K562	blood:
11	chr7:110890356..110892390-chr7:110893967..110896589,2	K562	blood:
12	chr7:111132967..111134732-chr7:111137505..111139653,3	MCF-7	breast:
13	chr7:111033479..111035253-chr7:111039939..111041629,3	K562	blood:
14	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
15	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
16	chr7:111075731..111078683-chr7:111110429..111113130,2	K562	blood:
17	chr7:110829508..110831617-chr7:110846112..110848748,2	K562	blood:
18	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
19	chr7:110838767..110841477-chr7:110867993..110870087,3	K562	blood:
20	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
21	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
22	chr12:108200986..108203742-chr7:111052172..111055145,3	MCF-7	breast:
23	chr7:110962126..110964268-chr7:110964422..110967257,2	K562	blood:
24	chr7:111070056..111074231-chr7:111075733..111078781,4	K562	blood:
25	chr7:110946494..110948605-chr7:110949688..110952299,2	K562	blood:
26	chr7:110845330..110847607-chr7:110862386..110864699,2	K562	blood:
27	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
28	chr7:111138086..111139591-chr7:111219192..111221961,2	MCF-7	breast:
29	chr7:111150770..111153588-chr7:111154725..111157322,3	K562	blood:
30	chr7:110838168..110840806-chr7:110845021..110846527,2	K562	blood:
31	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
32	chr7:110827684..110829363-chr7:110849997..110851639,2	K562	blood:
33	chr7:110843078..110844596-chr7:110851457..110854141,2	K562	blood:
34	chr7:110864193..110867019-chr7:110872692..110875184,2	K562	blood:
35	chr7:110948192..110950310-chr7:110952497..110954721,2	K562	blood:
36	chr7:111158021..111159788-chr7:111160191..111162474,2	K562	blood:
37	chr7:111033619..111035253-chr7:111039961..111041629,2	K562	blood:
38	chr7:110846458..110850024-chr7:110851219..110853852,3	MCF-7	breast:
39	chr7:110946449..110947994-chr7:110949688..110952187,2	K562	blood:
40	chr7:110901387..110901887-chr9:130159518..130160059,2	Hela-S3	cervix:
41	chr7:111030301..111032703-chr7:111035909..111038064,2	K562	blood:
42	chr7:110876830..110878652-chr7:110880390..110881983,2	K562	blood:
43	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
44	chr7:111103589..111105456-chr7:111112763..111114661,2	K562	blood:
45	chr7:110969600..110972534-chr7:111078171..111081389,3	K562	blood:
46	chr7:111012849..111014530-chr7:111019458..111021313,2	K562	blood:
47	chr7:110876830..110878652-chr7:110880390..110881983,2	K562	blood:
48	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
49	chr7:111099286..111101229-chr7:111113848..111115387,2	K562	blood:
50	chr7:111049337..111051671-chr7:111077981..111080558,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-7	chr7:110902289-110902553	expReg_chr7_8342_-

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
ENSG00000227948	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000136856	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 11689 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:11689 , 50 per page) page: 1 2 3 4 5 6 7 ... 234

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180759472	chr7:110821727-110821728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4730483	chr7:110821730-110821731	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs148758247	chr7:110821746-110821747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552399124	chr7:110821809-110821810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142409654	chr7:110821883-110821884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10262121	chr7:110821906-110821907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs554669930	chr7:110821924-110821925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs60913915	chr7:110821990-110821991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs537029055	chr7:110822055-110822056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139974776	chr7:110822094-110822095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576662394	chr7:110822099-110822100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10232632	chr7:110822114-110822115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs147663237	chr7:110822154-110822155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572273850	chr7:110822200-110822201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186566783	chr7:110822226-110822227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541151074	chr7:110822233-110822234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551416811	chr7:110822239-110822240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561027898	chr7:110822286-110822287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530075795	chr7:110822290-110822291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549468252	chr7:110822329-110822330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569932023	chr7:110822343-110822344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563482487	chr7:110822347-110822348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532440213	chr7:110822352-110822353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17441046	chr7:110822375-110822376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs565896378	chr7:110822399-110822400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57817514	chr7:110822400-110822401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs567387856	chr7:110822453-110822454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191013241	chr7:110822484-110822485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568131391	chr7:110822490-110822491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371291858	chr7:110822493-110822494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536685101	chr7:110822494-110822495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556378582	chr7:110822502-110822503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556909920	chr7:110822581-110822582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534667666	chr7:110822614-110822615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114893211	chr7:110822631-110822632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538954197	chr7:110822661-110822662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62466686	chr7:110822663-110822664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181267284	chr7:110822695-110822696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186279546	chr7:110822730-110822731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541213911	chr7:110822738-110822739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10281562	chr7:110822746-110822747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375153001	chr7:110822804-110822805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561087945	chr7:110822827-110822828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs58799975	chr7:110822836-110822837	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs58278550	chr7:110822850-110822851	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs373675228	chr7:110822909-110822910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563712006	chr7:110822913-110822914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370690600	chr7:110822939-110822940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532368285	chr7:110822976-110822977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190552503	chr7:110823001-110823002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110814000-110830600	Weak transcription	K562	blood
2	chr7:110816400-110830600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr7:110817800-110825200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr7:110820600-110824600	Weak transcription	Primary T cells from cord blood	blood
5	chr7:110822400-110822600	Enhancers	Duodenum Smooth Muscle	Duodenum
6	chr7:110822400-110823600	Enhancers	Fetal Lung	lung
7	chr7:110823000-110823800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr7:110823400-110824000	Enhancers	Fetal Heart	heart
9	chr7:110823400-110824000	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr7:110823600-110823800	Flanking Active TSS	Fetal Lung	lung
11	chr7:110823600-110824000	Enhancers	Fetal Brain Male	brain
12	chr7:110823800-110824000	Enhancers	Fetal Lung	lung
13	chr7:110824000-110824400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr7:110824000-110824800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr7:110824000-110825000	Weak transcription	Fetal Brain Male	brain
16	chr7:110824000-110825000	Weak transcription	Fetal Heart	heart
17	chr7:110824400-110825400	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr7:110824600-110825400	Enhancers	Primary T cells from cord blood	blood
19	chr7:110825000-110825200	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr7:110825000-110825400	Enhancers	Fetal Heart	heart
21	chr7:110825000-110825400	Enhancers	Psoas Muscle	Psoas
22	chr7:110825200-110825400	Enhancers	Fetal Brain Male	brain
23	chr7:110825200-110825400	Enhancers	NH-A	brain
24	chr7:110825400-110825600	Weak transcription	NH-A	brain
25	chr7:110825400-110833000	Weak transcription	Psoas Muscle	Psoas
26	chr7:110828000-110828400	Enhancers	Gastric	stomach
27	chr7:110830600-110830800	Enhancers	K562	blood
28	chr7:110830800-110831200	Flanking Active TSS	K562	blood
29	chr7:110830800-110831400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr7:110831200-110832000	Enhancers	K562	blood
31	chr7:110831400-110832800	Enhancers	A549	lung
32	chr7:110831600-110832000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:110831800-110833800	Enhancers	Liver	Liver
34	chr7:110832000-110832800	Weak transcription	K562	blood
35	chr7:110832400-110833400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:110832600-110833000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr7:110832600-110833200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:110832600-110833400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:110832600-110833600	Enhancers	HepG2	liver
40	chr7:110832800-110833000	Enhancers	K562	blood
41	chr7:110832800-110833200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr7:110832800-110833200	Flanking Active TSS	A549	lung
43	chr7:110832800-110833600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:110833000-110833200	Enhancers	Psoas Muscle	Psoas
45	chr7:110833000-110833400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:110833000-110833600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:110833000-110834200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr7:110833200-110833400	Active TSS	A549	lung
49	chr7:110833200-110833800	Weak transcription	Psoas Muscle	Psoas
50	chr7:110833400-110837800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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