Variant report

Variant	esv32879
Chromosome Location	chr7:150553149-150573695
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:427)
Chromatin interactive
region (count:33)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:150571844-150572195	GM12878	blood:	n/a	n/a
2	BCL3	chr7:150571848-150572248	GM12878	blood:	n/a	n/a
3	CEBPB	chr7:150568779-150568972	K562	blood:	n/a	n/a
4	CEBPB	chr7:150563533-150563818	A549	lung:	n/a	chr7:150563663-150563674 chr7:150563633-150563644
5	CEBPB	chr7:150563618-150563803	HepG2	liver:	n/a	chr7:150563663-150563674 chr7:150563633-150563644
6	CEBPB	chr7:150568768-150568949	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:150568807-150568991	A549	lung:	n/a	n/a
8	CTCF	chr7:150573096-150573156	MCF-7	breast:	n/a	n/a
9	CTCF	chr7:150572980-150573130	GM12865	blood:	n/a	n/a
10	CTCF	chr7:150572960-150573110	AG04450	lung:	n/a	n/a
11	CTCF	chr7:150557880-150558030	Caco-2	colon:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
12	CTCF	chr7:150572820-150573050	NHEK	skin:	n/a	n/a
13	CTCF	chr7:150572900-150573050	RPTEC	kidney:	n/a	n/a
14	CTCF	chr7:150572960-150573110	GM12864	blood:	n/a	n/a
15	CTCF	chr7:150557941-150558069	H1-hESC	embryonic stem cell:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
16	CTCF	chr7:150572980-150573130	GM12873	blood:	n/a	n/a
17	CTCF	chr7:150572980-150573130	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr7:150572936-150573147	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr7:150557900-150558050	Caco-2	colon:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
20	CTCF	chr7:150572980-150573130	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr7:150572967-150573085	LNCaP	prostate:	n/a	n/a
22	CTCF	chr7:150573000-150573150	HMF	breast:	n/a	n/a
23	CTCF	chr7:150558460-150558541	GM19239	blood:	n/a	n/a
24	CTCF	chr7:150573625-150574813	A549	lung:	n/a	chr7:150574014-150574035 chr7:150574013-150574029 chr7:150574372-150574381 chr7:150574012-150574030
25	CTCF	chr7:150557924-150558056	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
26	CTCF	chr7:150573017-150573142	GM10248	blood:	n/a	n/a
27	CTCF	chr7:150572780-150572930	NHLF	lung:	n/a	n/a
28	CTCF	chr7:150557980-150558034	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:150573020-150573170	GM06990	blood:	n/a	n/a
30	CTCF	chr7:150557900-150558050	SK-N-SH_RA	brain:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
31	CTCF	chr7:150572049-150572100	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:150572940-150573090	GM12869	blood:	n/a	n/a
33	CTCF	chr7:150573096-150573100	GM13977	blood:	n/a	n/a
34	CTCF	chr7:150572881-150573232	K562	blood:	n/a	n/a
35	CTCF	chr7:150557900-150558050	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
36	CTCF	chr7:150573000-150573150	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr7:150572920-150573070	GM12867	blood:	n/a	n/a
38	CTCF	chr7:150572920-150573070	HCFaa	heart:	n/a	n/a
39	CTCF	chr7:150572621-150573283	HCT-116	colon:	n/a	n/a
40	CTCF	chr7:150573000-150573150	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr7:150558120-150558270	K562	blood:	n/a	n/a
42	CTCF	chr7:150573240-150573390	GM12874	blood:	n/a	n/a
43	CTCF	chr7:150572960-150573110	GM12870	blood:	n/a	n/a
44	CTCF	chr7:150572920-150573070	AG10803	skin:	n/a	n/a
45	CTCF	chr7:150572991-150573148	HepG2	liver:	n/a	n/a
46	CTCF	chr7:150572980-150573130	GM12871	blood:	n/a	n/a
47	CTCF	chr7:150573020-150573170	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:150572933-150573212	K562	blood:	n/a	n/a
49	CTCF	chr7:150572920-150573070	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr7:150572960-150573110	GM12878	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150554420-150554470	Jurkat	blood:	n/a
2	chr7:150554113-150554163	AG09319	gingival:	n/a
3	chr7:150554628-150554678	AG10803	skin:	n/a
4	chr7:150554915-150554965	NHDF-neo	bronchial:	n/a
5	chr7:150554674-150554724	T-47D	breast:	n/a
6	chr7:150554674-150554724	AG04449	skin:	fetal
7	chr7:150554420-150554470	IMR90	lung:	fetal
8	chr7:150554113-150554163	GM06990	blood:	n/a
9	chr7:150554915-150554965	Jurkat	blood:	n/a
10	chr7:150558377-150558427	HAEpiC	amniotic membrane:	n/a
11	chr7:150554113-150554163	NB4	blood:	n/a
12	chr7:150554915-150554965	AG04450	lung:	fetal
13	chr7:150554628-150554678	HEK293	kidney:	embryo
14	chr7:150554674-150554724	AG09309	skin:	n/a
15	chr7:150555302-150555352	HCF	heart:	n/a
16	chr7:150554420-150554470	GM12878	blood:	n/a
17	chr7:150555302-150555352	HAEpiC	amniotic membrane:	n/a
18	chr7:150554420-150554470	MCF10A-Er-Src	breast:	n/a
19	chr7:150558377-150558427	AG04450	lung:	fetal
20	chr7:150558377-150558427	AoSMC	blood vessel:	n/a
21	chr7:150554674-150554724	MCF10A-Er-Src	breast:	n/a
22	chr7:150558377-150558427	HCT-116	colon:	n/a
23	chr7:150554113-150554163	PANC-1	pancreas:	n/a
24	chr7:150554420-150554470	CMK	blood:	n/a
25	chr7:150554674-150554724	K562	blood:	n/a
26	chr7:150554113-150554163	NT2-D1	testis:	n/a
27	chr7:150554420-150554470	PrEC	prostate:	n/a
28	chr7:150554674-150554724	CMK	blood:	n/a
29	chr7:150554113-150554163	Caco-2	colon:	n/a
30	chr7:150554628-150554678	GM06990	blood:	n/a
31	chr7:150554113-150554163	PrEC	prostate:	n/a
32	chr7:150554915-150554965	HCF	heart:	n/a
33	chr7:150554113-150554163	GM12892	blood:	n/a
34	chr7:150555302-150555352	SAEC	small airway:	n/a
35	chr7:150554915-150554965	HRCEpiC	kidney:	n/a
36	chr7:150554674-150554724	HAEpiC	amniotic membrane:	n/a
37	chr7:150554628-150554678	SK-N-SH_RA	brain:	n/a
38	chr7:150554113-150554163	HL-60	blood:	n/a
39	chr7:150554420-150554470	HL-60	blood:	n/a
40	chr7:150554420-150554470	HRPEpiC	eye:	n/a
41	chr7:150558377-150558427	Hela-S3	cervix:	n/a
42	chr7:150554674-150554724	PFSK-1	brain:	n/a
43	chr7:150554113-150554163	NHBE	bronchial:	n/a
44	chr7:150558377-150558427	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:150555302-150555352	HCM	heart:	n/a
46	chr7:150554915-150554965	HEEpiC	esophagus:	n/a
47	chr7:150554628-150554678	Hela-S3	cervix:	n/a
48	chr7:150555302-150555352	IMR90	lung:	fetal
49	chr7:150554113-150554163	SK-N-SH	brain:	n/a
50	chr7:150555302-150555352	AG10803	skin:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150564458..150567179-chr7:150567861..150571641,4	K562	blood:
2	chr7:150573002..150574576-chr7:150869374..150870431,9	K562	blood:
3	chr7:150562856..150565769-chr7:150566346..150570295,3	K562	blood:
4	chr7:150475526..150476482-chr7:150573625..150574754,8	MCF-7	breast:
5	chr7:150573562..150577370-chr7:150577412..150580576,4	K562	blood:
6	chr7:150550808..150555015-chr7:150558384..150561943,5	K562	blood:
7	chr7:150567773..150569879-chr7:150653213..150655593,2	K562	blood:
8	chr7:150564868..150567649-chr7:150590717..150593691,2	K562	blood:
9	chr7:150521643..150523890-chr7:150556049..150558134,2	K562	blood:
10	chr7:150477211..150477855-chr7:150573375..150574392,3	K562	blood:
11	chr7:150556165..150558158-chr7:150561303..150563873,2	K562	blood:
12	chr7:150573077..150574072-chr7:150683253..150683875,2	K562	blood:
13	chr7:150570270..150572638-chr7:150573385..150575681,2	K562	blood:
14	chr7:150550808..150553153-chr7:150558456..150560989,3	K562	blood:
15	chr7:150570270..150572638-chr7:150573385..150575681,2	K562	blood:
16	chr7:150568033..150570583-chr7:150684396..150686354,2	MCF-7	breast:
17	chr7:150547227..150549974-chr7:150551519..150553271,2	K562	blood:
18	chr7:150541762..150544255-chr7:150551164..150553467,2	K562	blood:
19	chr20:46012793..46013386-chr7:150572985..150573564,2	MCF-7	breast:
20	chr7:150550808..150555015-chr7:150558384..150561943,5	K562	blood:
21	chr7:150564458..150567179-chr7:150567861..150571641,4	K562	blood:
22	chr7:150475264..150476504-chr7:150573512..150575222,24	MCF-7	breast:
23	chr12:58153738..58156431-chr7:150562978..150565095,2	MCF-7	breast:
24	chr7:150562856..150565769-chr7:150566346..150570295,3	K562	blood:
25	chr7:150572726..150575481-chr7:150755589..150757663,2	K562	blood:
26	chr7:150550808..150553153-chr7:150558456..150560989,3	K562	blood:
27	chr7:150572299..150575283-chr7:150617480..150621735,3	K562	blood:
28	chr7:150475409..150476275-chr7:150572596..150573318,2	MCF-7	breast:
29	chr7:150556165..150558158-chr7:150561303..150563873,2	K562	blood:
30	chr7:150484477..150485748-chr7:150573549..150574883,10	MCF-7	breast:
31	chr7:150570280..150573172-chr7:150702825..150704695,2	K562	blood:
32	chr7:150542584..150544794-chr7:150560485..150563293,2	MCF-7	breast:
33	chr7:150572964..150574021-chr7:150869365..150870354,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABP1-2	chr7:150568389-150569059	predAs_engstrom06_BM715580_1
2	lnc-ABP1-1	chr7:150568035-150568307	expRegAs_chr7_12357_+

No data

Variant related genes	Relation type
AOC1	TF binding region
AOC1	CpG island
ENSG00000164885	chromatin interactions
ENSG00000002726	chromatin interactions
ENSG00000164889	chromatin interactions

Extended variants
information (count: 935 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:935 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58962017	chr7:150553168-150553169	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs557230859	chr7:150553171-150553172	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs59636768	chr7:150553254-150553255	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573786554	chr7:150553349-150553350	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs146252614	chr7:150553375-150553376	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs2071513	chr7:150553378-150553379	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs374072077	chr7:150553389-150553390	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572435011	chr7:150553393-150553394	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541869477	chr7:150553398-150553399	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564139159	chr7:150553435-150553436	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs533487887	chr7:150553450-150553451	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs45515699	chr7:150553469-150553470	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs10156189	chr7:150553475-150553476	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs564387925	chr7:150553528-150553529	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs139281415	chr7:150553551-150553552	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs370750286	chr7:150553553-150553554	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs549275999	chr7:150553554-150553555	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs547057578	chr7:150553563-150553564	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs565800850	chr7:150553564-150553565	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs373457221	chr7:150553566-150553567	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs531182439	chr7:150553579-150553580	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs200422035	chr7:150553586-150553587	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs377703686	chr7:150553591-150553592	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs10156191	chr7:150553605-150553606	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs374700351	chr7:150553606-150553607	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs367665701	chr7:150553614-150553615	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs571251831	chr7:150553616-150553617	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201476675	chr7:150553626-150553627	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs186258416	chr7:150553627-150553628	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs373918366	chr7:150553628-150553629	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs368128052	chr7:150553675-150553676	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs369957891	chr7:150553690-150553691	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs368309367	chr7:150553702-150553703	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs117779040	chr7:150553717-150553718	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs563618391	chr7:150553727-150553728	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs190863344	chr7:150553735-150553736	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs202051008	chr7:150553744-150553745	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs552872356	chr7:150553762-150553763	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200206369	chr7:150553831-150553832	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs375216693	chr7:150553833-150553834	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs368493191	chr7:150553838-150553839	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs572549369	chr7:150553842-150553843	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs144106544	chr7:150553850-150553851	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs79934982	chr7:150553851-150553852	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs577618065	chr7:150553856-150553857	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs368923061	chr7:150553858-150553859	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs373164869	chr7:150553888-150553889	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375159199	chr7:150553894-150553895	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs181034632	chr7:150553934-150553935	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs369516482	chr7:150553960-150553961	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Wilms tumour	21544195	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150539600-150553800	Weak transcription	Liver	Liver
2	chr7:150543200-150557600	Weak transcription	Right Atrium	heart
3	chr7:150549600-150553600	Weak transcription	Spleen	Spleen
4	chr7:150549800-150557400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr7:150549800-150558400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:150550000-150557400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:150550400-150553800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr7:150550600-150553600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr7:150550600-150555000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr7:150551400-150554400	Weak transcription	Colonic Mucosa	Colon
11	chr7:150551600-150553600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr7:150551800-150553800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:150552000-150553400	Enhancers	Placenta	Placenta
14	chr7:150552200-150553800	Enhancers	HMEC	breast
15	chr7:150552400-150553600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr7:150552400-150553800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:150552600-150553600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr7:150552800-150553200	Weak transcription	Fetal Intestine Small	intestine
19	chr7:150552800-150553600	Enhancers	NHEK	skin
20	chr7:150552800-150553800	Weak transcription	Fetal Intestine Large	intestine
21	chr7:150553000-150553600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:150553000-150553600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:150553200-150553600	Enhancers	Placenta Amnion	Placenta Amnion
24	chr7:150553200-150558800	Strong transcription	Fetal Intestine Small	intestine
25	chr7:150553400-150554200	Bivalent Enhancer	Placenta	Placenta
26	chr7:150553600-150553800	Flanking Active TSS	Spleen	Spleen
27	chr7:150553600-150554000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:150553600-150558800	Strong transcription	Rectal Mucosa Donor 31	rectum
29	chr7:150553600-150559400	Strong transcription	Duodenum Mucosa	Duodenum
30	chr7:150553800-150555200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:150553800-150555400	Strong transcription	Liver	Liver
32	chr7:150553800-150556400	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:150553800-150557400	Weak transcription	Spleen	Spleen
34	chr7:150553800-150558600	Strong transcription	Fetal Intestine Large	intestine
35	chr7:150554000-150556200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:150554400-150554800	Strong transcription	Colonic Mucosa	Colon
37	chr7:150554800-150555800	Weak transcription	Colonic Mucosa	Colon
38	chr7:150555000-150561400	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr7:150555200-150556200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:150555400-150556000	Bivalent Enhancer	Placenta	Placenta
41	chr7:150555400-150564000	Weak transcription	Liver	Liver
42	chr7:150555800-150556200	Strong transcription	Colonic Mucosa	Colon
43	chr7:150556200-150557400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:150556200-150557600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:150556200-150557600	Weak transcription	Colonic Mucosa	Colon
46	chr7:150556400-150557800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr7:150557400-150557800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:150557400-150557800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr7:150557400-150558200	ZNF genes & repeats	Spleen	Spleen
50	chr7:150557400-150558400	Enhancers	H1 Cell Line	embryonic stem cell

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