Variant report

Variant	esv16850
Chromosome Location	chr7:97502248-97578516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:97532399-97532863	GM12878	blood:	n/a	n/a
2	BATF	chr7:97517798-97518101	GM12878	blood:	n/a	n/a
3	BATF	chr7:97544706-97545031	GM12878	blood:	n/a	n/a
4	BATF	chr7:97508909-97509359	GM12878	blood:	n/a	n/a
5	BATF	chr7:97517863-97518077	GM12878	blood:	n/a	n/a
6	BATF	chr7:97545127-97545322	GM12878	blood:	n/a	n/a
7	BATF	chr7:97541709-97541900	GM12878	blood:	n/a	n/a
8	BATF	chr7:97544753-97545017	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:97509132-97509377	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:97538914-97539187	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:97503987-97504184	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:97508956-97509366	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:97544694-97544995	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:97537513-97537758	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:97544643-97545002	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:97545138-97545312	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:97502687-97502693	K562	blood:	n/a	n/a
18	BHLHE40	chr7:97501010-97502256	K562	blood:	n/a	chr7:97501392-97501408
19	CBX3	chr7:97508766-97509173	K562	blood:	n/a	n/a
20	CBX3	chr7:97508845-97509104	K562	blood:	n/a	n/a
21	CEBPB	chr7:97557830-97557832	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:97545613-97545876	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:97559008-97559085	HepG2	liver:	n/a	chr7:97559036-97559047 chr7:97559038-97559047 chr7:97559036-97559049
24	CHD1	chr7:97557647-97557768	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:97521100-97521250	HepG2	liver:	n/a	n/a
26	CTCF	chr7:97541634-97542016	A549	lung:	n/a	n/a
27	CTCF	chr7:97544568-97544590	Medullo	brain:	n/a	n/a
28	CTCF	chr7:97557700-97557850	AG04450	lung:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
29	CTCF	chr7:97557740-97557890	GM12868	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
30	CTCF	chr7:97557700-97557850	HBMEC	blood vessel:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
31	CTCF	chr7:97557720-97557870	HepG2	liver:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
32	CTCF	chr7:97557720-97557870	HAc	cerebellar:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
33	CTCF	chr7:97557720-97557870	WI-38	lung:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
34	CTCF	chr7:97557740-97557890	GM12870	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
35	CTCF	chr7:97557636-97557945	GM10248	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
36	CTCF	chr7:97557720-97557870	NHDF-neo	bronchial:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
37	CTCF	chr7:97521208-97521237	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:97557700-97557850	HRE	kidney:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
39	CTCF	chr7:97521080-97521230	GM12872	blood:	n/a	n/a
40	CTCF	chr7:97557980-97558130	HPF	lung:	n/a	n/a
41	CTCF	chr7:97557980-97558130	AG09319	gingival:	n/a	n/a
42	CTCF	chr7:97557680-97557830	AoAF	blood vessel:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
43	CTCF	chr7:97558220-97558370	HCM	heart:	n/a	n/a
44	CTCF	chr7:97557643-97557921	Lung_OC	lung:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
45	CTCF	chr7:97553720-97553746	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr7:97557700-97557850	NB4	blood:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
47	CTCF	chr7:97557644-97557955	LNCaP	prostate:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
48	CTCF	chr7:97557680-97557830	HRE	kidney:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
49	CTCF	chr7:97557720-97557870	HEEpiC	esophagus:	n/a	chr7:97557774-97557787 chr7:97557773-97557789 chr7:97557772-97557790 chr7:97557767-97557788 chr7:97557774-97557787
50	CTCF	chr7:97558020-97558170	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97557830-97557880	SAEC	small airway:	n/a
2	chr7:97557830-97557880	SAEC	small airway:	n/a
3	chr7:97565504-97565554	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:97558753-97558803	ECC-1	luminal epithelium:	n/a
5	chr7:97568024-97568074	SK-N-SH	brain:	n/a
6	chr7:97557827-97557877	HIPEpiC	eye:	n/a
7	chr7:97565354-97565404	ECC-1	luminal epithelium:	n/a
8	chr7:97553776-97553826	HEK293	kidney:	embryo
9	chr7:97502647-97502697	PFSK-1	brain:	n/a
10	chr7:97557830-97557880	HepG2	liver:	n/a
11	chr7:97557134-97557184	HUVEC	blood vessel:	n/a
12	chr7:97557830-97557880	Caco-2	colon:	n/a
13	chr7:97568664-97568714	GM12878	blood:	n/a
14	chr7:97557298-97557348	HEK293	kidney:	embryo
15	chr7:97568024-97568074	SAEC	small airway:	n/a
16	chr7:97557827-97557877	GM12878	blood:	n/a
17	chr7:97565354-97565404	GM12891	blood:	n/a
18	chr7:97557830-97557880	GM06990	blood:	n/a
19	chr7:97505608-97505658	SK-N-SH_RA	brain:	n/a
20	chr7:97557827-97557877	HRE	kidney:	n/a
21	chr7:97557134-97557184	SK-N-SH	brain:	n/a
22	chr7:97558075-97558125	ProgFib	skin:	n/a
23	chr7:97570449-97570499	GM12878	blood:	n/a
24	chr7:97567812-97567862	BJ	skin:	n/a
25	chr7:97505608-97505658	Hepatocyte	liver:	n/a
26	chr7:97570449-97570499	PrEC	prostate:	n/a
27	chr7:97565354-97565404	LNCaP	prostate:	n/a
28	chr7:97568664-97568714	HAEpiC	amniotic membrane:	n/a
29	chr7:97568664-97568714	AG04450	lung:	fetal
30	chr7:97557134-97557184	HRPEpiC	eye:	n/a
31	chr7:97565504-97565554	HL-60	blood:	n/a
32	chr7:97553776-97553826	HIPEpiC	eye:	n/a
33	chr7:97558075-97558125	LNCaP	prostate:	n/a
34	chr7:97557134-97557184	AG10803	skin:	n/a
35	chr7:97558075-97558125	Hela-S3	cervix:	n/a
36	chr7:97558075-97558125	AoSMC	blood vessel:	n/a
37	chr7:97502647-97502697	AG09319	gingival:	n/a
38	chr7:97557830-97557880	PFSK-1	brain:	n/a
39	chr7:97570449-97570499	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:97553776-97553826	GM12891	blood:	n/a
41	chr7:97558753-97558803	HAEpiC	amniotic membrane:	n/a
42	chr7:97557134-97557184	PFSK-1	brain:	n/a
43	chr7:97557134-97557184	H1-hESC	embryonic stem cell:	embryo
44	chr7:97505608-97505658	SAEC	small airway:	n/a
45	chr7:97565504-97565554	RPTEC	kidney:	n/a
46	chr7:97568024-97568074	AoSMC	blood vessel:	n/a
47	chr7:97557298-97557348	GM12891	blood:	n/a
48	chr7:97557298-97557348	LNCaP	prostate:	n/a
49	chr7:97502647-97502697	HIPEpiC	eye:	n/a
50	chr7:97502647-97502697	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:97464795..97465461-chr7:97557301..97558244,2	K562	blood:
2	chr7:97499263..97502446-chr7:97599755..97603082,5	K562	blood:
3	chr7:96733769..96734552-chr7:97557710..97558244,2	MCF-7	breast:
4	chr7:97501305..97502999-chr7:98028998..98030520,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAC1-3	chr7:97535741-97536134	NONHSAT122154
2	lnc-TAC1-1	chr7:97512594-97513107	NONHSAT122151
3	lnc-TAC1-2	chr7:97515180-97515386	NONHSAT122152

Variant related genes	Relation type
ENSG00000232097	TF binding region
RPS3AP29	TF binding region
ASNS	TF binding region
ENSG00000231812	TF binding region
ENSG00000221048	TF binding region
ENSG00000232032	TF binding region
ENSG00000235982	TF binding region
ENSG00000231859	TF binding region
OR7E7P	TF binding region
ENSG00000232097	CpG island
RPS3AP29	CpG island
ASNS	CpG island
ENSG00000231812	CpG island
ENSG00000221048	CpG island
ENSG00000232032	CpG island
ENSG00000235982	CpG island
ENSG00000231859	CpG island
OR7E7P	CpG island
ENSG00000006453	chromatin interactions
ENSG00000243554	chromatin interactions

Extended variants
information (count: 2485 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2485 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3757675	chr7:97502322-97502323	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543717087	chr7:97502372-97502373	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs145199879	chr7:97502427-97502428	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs577163349	chr7:97502458-97502459	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74468320	chr7:97502509-97502510	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs148705224	chr7:97502554-97502555	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs183371066	chr7:97502631-97502632	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370511109	chr7:97502724-97502725	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs1974562	chr7:97502737-97502738	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs186277496	chr7:97502788-97502789	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548673202	chr7:97502812-97502813	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs539139763	chr7:97502856-97502857	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566995767	chr7:97502880-97502881	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549758467	chr7:97503008-97503009	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs571557209	chr7:97503027-97503028	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs538970234	chr7:97503065-97503066	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs142271605	chr7:97503074-97503075	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs566101701	chr7:97503082-97503083	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs536314722	chr7:97503087-97503088	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs3757674	chr7:97503140-97503141	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs561419832	chr7:97503217-97503218	Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs147914420	chr7:97503433-97503434	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs2681164	chr7:97503471-97503472	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs558764710	chr7:97503492-97503493	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs34980123	chr7:97503494-97503495	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs77485454	chr7:97503517-97503518	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs75385699	chr7:97503518-97503519	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577104869	chr7:97503556-97503557	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs541351188	chr7:97503560-97503561	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs377447740	chr7:97503601-97503602	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs559689007	chr7:97503647-97503648	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs74874057	chr7:97503731-97503732	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs13311082	chr7:97503744-97503745	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs572019451	chr7:97503755-97503756	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs141625531	chr7:97503777-97503778	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561037064	chr7:97503801-97503802	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs13311018	chr7:97503804-97503805	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs10234646	chr7:97503807-97503808	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543588149	chr7:97503855-97503856	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs10234781	chr7:97503913-97503914	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532420063	chr7:97503929-97503930	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs547729762	chr7:97503936-97503937	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs566038217	chr7:97503947-97503948	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs530109274	chr7:97503958-97503959	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548338793	chr7:97503996-97503997	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs111517880	chr7:97504015-97504016	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs183701075	chr7:97504035-97504036	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs188417049	chr7:97504057-97504058	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs570124814	chr7:97504059-97504060	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs537180721	chr7:97504060-97504061	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97500000-97502400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:97500400-97502400	Active TSS	Breast Myoepithelial Primary Cells	Breast
3	chr7:97500400-97502400	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr7:97500400-97502400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr7:97500600-97502400	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr7:97500600-97502400	Active TSS	Colon Smooth Muscle	Colon
7	chr7:97500800-97502400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:97500800-97502400	Active TSS	Brain Anterior Caudate	brain
9	chr7:97501000-97502400	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr7:97501000-97502400	Active TSS	Fetal Brain Female	brain
11	chr7:97501000-97502400	Active TSS	Rectal Smooth Muscle	rectum
12	chr7:97501400-97502400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:97501400-97502400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:97501400-97502400	Active TSS	Fetal Intestine Large	intestine
15	chr7:97501800-97503000	Weak transcription	Esophagus	oesophagus
16	chr7:97501800-97503200	Enhancers	Spleen	Spleen
17	chr7:97502000-97502400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
18	chr7:97502000-97502400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:97502000-97502400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr7:97502000-97502400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:97502000-97502400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:97502000-97502400	Flanking Active TSS	Brain Angular Gyrus	brain
23	chr7:97502000-97502400	Flanking Active TSS	Brain Cingulate Gyrus	brain
24	chr7:97502000-97502400	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr7:97502000-97502400	Enhancers	Left Ventricle	heart
26	chr7:97502000-97502400	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr7:97502000-97502400	Flanking Active TSS	K562	blood
28	chr7:97502000-97503200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr7:97502200-97502400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr7:97502200-97502400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
31	chr7:97502200-97502400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr7:97502200-97502400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr7:97502200-97502400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr7:97502200-97502400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr7:97502200-97502400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:97502200-97502400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:97502200-97502400	Enhancers	Primary T cells fromperipheralblood	blood
38	chr7:97502200-97502400	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr7:97502200-97502400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr7:97502200-97502400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr7:97502200-97502400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:97502200-97502400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr7:97502200-97502400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr7:97502200-97502400	Enhancers	Aorta	Aorta
45	chr7:97502200-97502400	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr7:97502200-97502400	Enhancers	Fetal Intestine Small	intestine
47	chr7:97502200-97502400	Enhancers	Fetal Lung	lung
48	chr7:97502200-97502400	Enhancers	Fetal Muscle Trunk	muscle
49	chr7:97502200-97502400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr7:97502200-97502400	Enhancers	A549	lung

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