Variant report

Variant	nsv1028670
Chromosome Location	chr7:110803740-111035102
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1451)
CpG islands
(count:244)
Chromatin interactive
region (count:177)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1451 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110869353-110869485	K562	blood:	n/a	n/a
2	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
3	ARID3A	chr7:110821607-110821614	K562	blood:	n/a	n/a
4	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
5	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
6	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
7	ARID3A	chr7:110863537-110864343	K562	blood:	n/a	chr7:110863547-110863563 chr7:110863548-110863564
8	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
9	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
10	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
11	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
12	ARID3A	chr7:110832610-110833023	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
14	ARID3A	chr7:110830821-110831569	K562	blood:	n/a	n/a
15	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
16	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
18	ATF1	chr7:110863987-110864363	K562	blood:	n/a	n/a
19	ATF1	chr7:110830910-110831249	K562	blood:	n/a	n/a
20	ATF1	chr7:110889894-110890092	K562	blood:	n/a	n/a
21	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
22	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
23	ATF3	chr7:110838322-110838906	HCT-116	colon:	n/a	n/a
24	ATF3	chr7:110872430-110873085	A549	lung:	n/a	n/a
25	BACH1	chr7:110935269-110935465	K562	blood:	n/a	n/a
26	BACH1	chr7:110864793-110865013	K562	blood:	n/a	n/a
27	BATF	chr7:110960156-110960503	GM12878	blood:	n/a	n/a
28	BATF	chr7:110872606-110872814	GM12878	blood:	n/a	chr7:110872713-110872724 chr7:110872714-110872724
29	BATF	chr7:110992517-110992735	GM12878	blood:	n/a	n/a
30	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a
31	BATF	chr7:110872545-110872818	GM12878	blood:	n/a	chr7:110872713-110872724 chr7:110872714-110872724
32	BCL11A	chr7:111029036-111029324	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:110830940-110831167	K562	blood:	n/a	n/a
34	BHLHE40	chr7:110964357-110964616	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:110913546-110913742	K562	blood:	n/a	n/a
36	BHLHE40	chr7:110863735-110864331	K562	blood:	n/a	n/a
37	BHLHE40	chr7:110858674-110858794	K562	blood:	n/a	n/a
38	BHLHE40	chr7:110814285-110814288	K562	blood:	n/a	n/a
39	BRCA1	chr7:110838357-110838733	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr7:110838093-110838977	HCT-116	colon:	n/a	n/a
41	CBX3	chr7:110838198-110838910	HCT-116	colon:	n/a	n/a
42	CBX3	chr7:110863686-110864413	K562	blood:	n/a	n/a
43	CBX3	chr7:110830803-110831285	K562	blood:	n/a	n/a
44	CBX3	chr7:110983007-110983449	K562	blood:	n/a	n/a
45	CBX3	chr7:110910820-110911290	K562	blood:	n/a	n/a
46	CBX3	chr7:110969313-110970175	K562	blood:	n/a	n/a
47	CBX3	chr7:110983037-110983415	K562	blood:	n/a	n/a
48	CCNT2	chr7:110941498-110941584	K562	blood:	n/a	n/a
49	CCNT2	chr7:110895712-110896018	K562	blood:	n/a	n/a
50	CCNT2	chr7:110863845-110864310	K562	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	chr7:110838461-110838511	SK-N-SH	brain:	n/a
2	chr7:110879415-110879465	NHDF-neo	bronchial:	n/a
3	chr7:110906785-110906835	NH-A	brain:	n/a
4	chr7:110838461-110838511	BE2_C	brain:	n/a
5	chr7:110906785-110906835	GM12878	blood:	n/a
6	chr7:111033064-111033114	HUVEC	blood vessel:	n/a
7	chr7:110906785-110906835	HL-60	blood:	n/a
8	chr7:110838461-110838511	SK-N-SH_RA	brain:	n/a
9	chr7:110838461-110838511	HepG2	liver:	n/a
10	chr7:111033064-111033114	SAEC	small airway:	n/a
11	chr7:110906785-110906835	SK-N-SH_RA	brain:	n/a
12	chr7:110879415-110879465	HepG2	liver:	n/a
13	chr7:110838461-110838511	RPTEC	kidney:	n/a
14	chr7:110879415-110879465	HNPCEpiC	eye:	n/a
15	chr7:110879415-110879465	Caco-2	colon:	n/a
16	chr7:111033064-111033114	CMK	blood:	n/a
17	chr7:110838461-110838511	NT2-D1	testis:	n/a
18	chr7:110906785-110906835	HepG2	liver:	n/a
19	chr7:110906785-110906835	HMEC	breast:	n/a
20	chr7:111033064-111033114	HCT-116	colon:	n/a
21	chr7:110879415-110879465	HCM	heart:	n/a
22	chr7:110838461-110838511	Jurkat	blood:	n/a
23	chr7:110906785-110906835	ProgFib	skin:	n/a
24	chr7:111033064-111033114	HRE	kidney:	n/a
25	chr7:110906785-110906835	HCM	heart:	n/a
26	chr7:111033064-111033114	Hela-S3	cervix:	n/a
27	chr7:110879415-110879465	HRPEpiC	eye:	n/a
28	chr7:110879415-110879465	SAEC	small airway:	n/a
29	chr7:110879415-110879465	GM06990	blood:	n/a
30	chr7:111033064-111033114	MCF10A-Er-Src	breast:	n/a
31	chr7:110906785-110906835	GM19239	blood:	n/a
32	chr7:110906785-110906835	HCT-116	colon:	n/a
33	chr7:110838461-110838511	BJ	skin:	n/a
34	chr7:110906785-110906835	PrEC	prostate:	n/a
35	chr7:110879415-110879465	ovcar-3	ovarian:	n/a
36	chr7:111033064-111033114	HCM	heart:	n/a
37	chr7:110879415-110879465	GM19239	blood:	n/a
38	chr7:110906785-110906835	AG09319	gingival:	n/a
39	chr7:110838461-110838511	PANC-1	pancreas:	n/a
40	chr7:110906785-110906835	NHDF-neo	bronchial:	n/a
41	chr7:110879415-110879465	AG04450	lung:	fetal
42	chr7:110879415-110879465	HAEpiC	amniotic membrane:	n/a
43	chr7:110838461-110838511	AG09309	skin:	n/a
44	chr7:110838461-110838511	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:110838461-110838511	CMK	blood:	n/a
46	chr7:110838461-110838511	AG04450	lung:	fetal
47	chr7:110879415-110879465	BJ	skin:	n/a
48	chr7:111033064-111033114	HCF	heart:	n/a
49	chr7:110838461-110838511	ovcar-3	ovarian:	n/a
50	chr7:110879415-110879465	GM12891	blood:	n/a

(count:177 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:110807402..110810065-chr7:110811637..110813724,2	K562	blood:
2	chr7:111013152..111016122-chr7:111032306..111034572,2	K562	blood:
3	chr7:110907955..110909675-chr7:110912861..110914751,2	K562	blood:
4	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
5	chr7:110831361..110833166-chr7:110833300..110836060,2	K562	blood:
6	chr7:110838168..110840806-chr7:110845021..110846527,2	K562	blood:
7	chr7:110970018..110971875-chr7:110977199..110979815,2	K562	blood:
8	chr7:110991909..110993941-chr7:110997470..110999246,2	K562	blood:
9	chr7:111018357..111021397-chr7:111023712..111026997,4	K562	blood:
10	chr7:110858379..110861216-chr7:110867269..110869936,2	MCF-7	breast:
11	chr7:111027546..111029195-chr7:111032815..111035330,2	K562	blood:
12	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
13	chr7:110973996..110977417-chr7:110978130..110980823,3	K562	blood:
14	chr7:110827684..110829363-chr7:110849997..110851639,2	K562	blood:
15	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
16	chr7:110910606..110912820-chr7:110916912..110919074,2	K562	blood:
17	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
18	chr7:110910606..110912820-chr7:110916912..110919074,2	K562	blood:
19	chr7:111014312..111015875-chr7:111016018..111018954,2	MCF-7	breast:
20	chr7:110827684..110829363-chr7:110849997..110851639,2	K562	blood:
21	chr7:111003207..111005251-chr7:111008050..111010228,2	K562	blood:
22	chr5:125812513..125813255-chr7:110998210..110998982,2	MCF-7	breast:
23	chr7:110890356..110892390-chr7:110893967..110896589,2	K562	blood:
24	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
25	chr7:110828459..110830042-chr7:110834757..110837365,2	K562	blood:
26	chr7:110968689..110972135-chr7:110972915..110976641,3	K562	blood:
27	chr7:110977304..110981066-chr7:110982767..110987604,6	K562	blood:
28	chr7:111001961..111006807-chr7:111013802..111016795,4	K562	blood:
29	chr7:110846499..110848352-chr7:110867218..110869031,2	MCF-7	breast:
30	chr7:110901427..110902958-chr7:110904579..110907166,2	MCF-7	breast:
31	chr7:110964713..110967341-chr7:110967524..110969143,2	K562	blood:
32	chr7:110822071..110825302-chr7:110827142..110830150,3	K562	blood:
33	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
34	chr7:110836787..110838968-chr7:110842164..110843669,2	K562	blood:
35	chr7:110985007..110987369-chr7:110994363..110996141,2	K562	blood:
36	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
37	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
38	chr7:110860948..110867491-chr7:110867576..110875570,9	K562	blood:
39	chr7:110901427..110902958-chr7:110904579..110907166,2	MCF-7	breast:
40	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
41	chr7:110838168..110840806-chr7:110845021..110846527,2	K562	blood:
42	chr7:110955341..110956918-chr7:110957234..110959729,2	K562	blood:
43	chr7:110934094..110935861-chr7:110939196..110941083,3	K562	blood:
44	chr7:110989989..110992007-chr7:110993979..110995982,2	K562	blood:
45	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
46	chr7:110983062..110985792-chr7:110987528..110989399,4	K562	blood:
47	chr7:110941905..110944454-chr7:110944620..110946786,2	K562	blood:
48	chr7:110953570..110955733-chr7:111376151..111377847,2	MCF-7	breast:
49	chr7:110867615..110869914-chr7:110870998..110874841,5	K562	blood:
50	chr7:110963413..110966213-chr7:110967085..110969024,2	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
ENSG00000243621	TF binding region
IMMP2L	TF binding region
ENSG00000243621	CpG island
IMMP2L	CpG island
ENSG00000136856	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000184903	chromatin interactions

Extended variants
information (count: 7903 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:7903 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149216075	chr7:110803761-110803762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564524951	chr7:110803788-110803789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs578086576	chr7:110803837-110803838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540588318	chr7:110803838-110803839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571597054	chr7:110803910-110803911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560221773	chr7:110803922-110803923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191655653	chr7:110803951-110803952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576289907	chr7:110803964-110803965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183469099	chr7:110804022-110804023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142476186	chr7:110804095-110804096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531364067	chr7:110804153-110804154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372968953	chr7:110804155-110804156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148915362	chr7:110804198-110804199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372566721	chr7:110804217-110804218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58271541	chr7:110804241-110804242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555085255	chr7:110804308-110804309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561857119	chr7:110804315-110804316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76910825	chr7:110804337-110804338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373049508	chr7:110804343-110804344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187922584	chr7:110804354-110804355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192635891	chr7:110804368-110804369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536136635	chr7:110804411-110804412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540629100	chr7:110804425-110804426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376021059	chr7:110804456-110804457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183346164	chr7:110804522-110804523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531394717	chr7:110804536-110804537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547496039	chr7:110804547-110804548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146840813	chr7:110804567-110804568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140676655	chr7:110804582-110804583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145674191	chr7:110804674-110804675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186902546	chr7:110804675-110804676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540296762	chr7:110804715-110804716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192663682	chr7:110804746-110804747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573896172	chr7:110804751-110804752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542920183	chr7:110804767-110804768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562398707	chr7:110804790-110804791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531426678	chr7:110804859-110804860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76391174	chr7:110804863-110804864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138331466	chr7:110804864-110804865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527374834	chr7:110804934-110804935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547115087	chr7:110804978-110804979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184834306	chr7:110805007-110805008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529610702	chr7:110805075-110805076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189727432	chr7:110805079-110805080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549750680	chr7:110805192-110805193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192912233	chr7:110805209-110805210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10227865	chr7:110805249-110805250	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs558361933	chr7:110805292-110805293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34508148	chr7:110805345-110805346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140912180	chr7:110805412-110805413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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

Chromatin state (count:1044 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110799600-110804400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:110803400-110808000	Weak transcription	Lung	lung
3	chr7:110804400-110804600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:110804400-110805200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:110804600-110805400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr7:110805000-110805400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:110805400-110807000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr7:110805400-110807400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:110805800-110806000	Enhancers	Psoas Muscle	Psoas
10	chr7:110806600-110806800	Enhancers	Psoas Muscle	Psoas
11	chr7:110807000-110809200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr7:110807400-110809000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:110807800-110808600	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr7:110808200-110808600	Enhancers	NHDF-Ad	bronchial
15	chr7:110808200-110809000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:110808400-110808600	Enhancers	Colon Smooth Muscle	Colon
17	chr7:110808400-110808600	Enhancers	Fetal Brain Male	brain
18	chr7:110808400-110808800	Enhancers	Rectal Smooth Muscle	rectum
19	chr7:110808600-110812600	Weak transcription	Colon Smooth Muscle	Colon
20	chr7:110808600-110814000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr7:110808800-110812800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr7:110812400-110813600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:110812600-110813000	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr7:110812600-110814800	Enhancers	Colon Smooth Muscle	Colon
25	chr7:110812800-110813200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:110812800-110813600	Enhancers	Rectal Smooth Muscle	rectum
27	chr7:110812800-110813600	Enhancers	K562	blood
28	chr7:110813600-110814000	Flanking Active TSS	K562	blood
29	chr7:110814000-110814600	Enhancers	Brain Germinal Matrix	brain
30	chr7:110814000-110815000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:110814000-110830600	Weak transcription	K562	blood
32	chr7:110814600-110815000	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr7:110815000-110815600	Enhancers	Brain Germinal Matrix	brain
34	chr7:110815800-110816600	Enhancers	Primary T cells from cord blood	blood
35	chr7:110815800-110816600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:110816200-110816400	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr7:110816200-110816600	Enhancers	Dnd41	blood
38	chr7:110816200-110816800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr7:110816400-110830600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr7:110816600-110819600	Weak transcription	Primary T cells from cord blood	blood
41	chr7:110817800-110825200	Weak transcription	Primary hematopoietic stem cells	blood
42	chr7:110819400-110820200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
43	chr7:110819400-110820200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:110819600-110820600	Strong transcription	Primary T cells from cord blood	blood
45	chr7:110820600-110824600	Weak transcription	Primary T cells from cord blood	blood
46	chr7:110822400-110822600	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr7:110822400-110823600	Enhancers	Fetal Lung	lung
48	chr7:110823000-110823800	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr7:110823400-110824000	Enhancers	Fetal Heart	heart
50	chr7:110823400-110824000	Enhancers	Skeletal Muscle Female	skeletal muscle

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