Variant report

Variant	esv1849580
Chromosome Location	chr7:97846435-97860164
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:732)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 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	ARID3A	chr7:97847663-97847944	K562	blood:	n/a	n/a
2	ARID3A	chr7:97855510-97855782	HepG2	liver:	n/a	n/a
3	ATF2	chr7:97849099-97849509	GM12878	blood:	n/a	n/a
4	ATF2	chr7:97848596-97849007	GM12878	blood:	n/a	n/a
5	BATF	chr7:97848680-97848997	GM12878	blood:	n/a	n/a
6	BATF	chr7:97848653-97849003	GM12878	blood:	n/a	n/a
7	BCLAF1	chr7:97848668-97849063	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:97848682-97848872	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:97849181-97849480	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:97846978-97847938	K562	blood:	n/a	chr7:97847399-97847415
11	CBX3	chr7:97847579-97847944	K562	blood:	n/a	n/a
12	CCNT2	chr7:97857856-97857921	K562	blood:	n/a	n/a
13	CCNT2	chr7:97847291-97847938	K562	blood:	n/a	n/a
14	CEBPB	chr7:97857558-97857722	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
15	CEBPB	chr7:97857460-97857814	HepG2	liver:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
16	CEBPB	chr7:97857410-97857839	MCF-7	breast:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
17	CEBPB	chr7:97857541-97857759	H1-hESC	embryonic stem cell:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
18	CEBPB	chr7:97857556-97857798	Hela-S3	cervix:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
19	CEBPB	chr7:97857468-97857755	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
20	CEBPB	chr7:97857468-97857829	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
21	CEBPB	chr7:97849858-97849970	K562	blood:	n/a	n/a
22	CEBPB	chr7:97857481-97857783	IMR90	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
23	CEBPB	chr7:97847691-97847919	K562	blood:	n/a	n/a
24	CEBPB	chr7:97857458-97857785	A549	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
25	CTCF	chr7:97859593-97859672	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:97859560-97859710	GM12870	blood:	n/a	n/a
27	CTCF	chr7:97859540-97859690	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr7:97859540-97859690	GM12873	blood:	n/a	n/a
29	CTCF	chr7:97859554-97859689	GM12891	blood:	n/a	n/a
30	CTCF	chr7:97859560-97859710	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr7:97859559-97859657	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr7:97859540-97859690	GM12868	blood:	n/a	n/a
33	CTCF	chr7:97859500-97859650	GM12873	blood:	n/a	n/a
34	CTCF	chr7:97854030-97854041	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:97859611-97859660	K562	blood:	n/a	n/a
36	CTCF	chr7:97859595-97859662	HepG2	liver:	n/a	n/a
37	CTCF	chr7:97859564-97859690	GM19238	blood:	n/a	n/a
38	CTCF	chr7:97859586-97859663	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:97859505-97859705	GM12878	blood:	n/a	n/a
40	CTCF	chr7:97853955-97854015	H1-hESC	embryonic stem cell:	n/a	chr7:97853977-97853986
41	CTCF	chr7:97859520-97859670	GM12873	blood:	n/a	n/a
42	CTCF	chr7:97859600-97859750	GM12864	blood:	n/a	n/a
43	CTCF	chr7:97859560-97859710	A549	lung:	n/a	n/a
44	CTCF	chr7:97847719-97847901	K562	blood:	n/a	n/a
45	CTCF	chr7:97859547-97859690	GM12892	blood:	n/a	n/a
46	CTCF	chr7:97858895-97858946	GM20000	blood:	n/a	n/a
47	CTCF	chr7:97859560-97859710	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr7:97859588-97859689	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:97859562-97859687	K562	blood:	n/a	n/a
50	CTCF	chr7:97859483-97859700	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97847111-97847161	HEEpiC	esophagus:	n/a
2	chr7:97857492-97857542	GM12891	blood:	n/a
3	chr7:97857989-97858039	BJ	skin:	n/a
4	chr7:97847054-97847104	NHDF-neo	bronchial:	n/a
5	chr7:97857971-97858021	HNPCEpiC	eye:	n/a
6	chr7:97857971-97858021	SK-N-SH	brain:	n/a
7	chr7:97857989-97858039	HMEC	breast:	n/a
8	chr7:97857647-97857697	HRPEpiC	eye:	n/a
9	chr7:97857492-97857542	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:97857989-97858039	HAEpiC	amniotic membrane:	n/a
11	chr7:97857938-97857988	HIPEpiC	eye:	n/a
12	chr7:97857971-97858021	Jurkat	blood:	n/a
13	chr7:97846988-97847038	GM12891	blood:	n/a
14	chr7:97852022-97852072	HMEC	breast:	n/a
15	chr7:97847111-97847161	AG10803	skin:	n/a
16	chr7:97857647-97857697	AG09319	gingival:	n/a
17	chr7:97857971-97858021	IMR90	lung:	fetal
18	chr7:97857938-97857988	PrEC	prostate:	n/a
19	chr7:97847054-97847104	AG04450	lung:	fetal
20	chr7:97857938-97857988	HNPCEpiC	eye:	n/a
21	chr7:97857989-97858039	AG04450	lung:	fetal
22	chr7:97847054-97847104	HNPCEpiC	eye:	n/a
23	chr7:97847054-97847104	HRE	kidney:	n/a
24	chr7:97857647-97857697	LNCaP	prostate:	n/a
25	chr7:97847054-97847104	IMR90	lung:	fetal
26	chr7:97857647-97857697	NHBE	bronchial:	n/a
27	chr7:97851854-97851904	NT2-D1	testis:	n/a
28	chr7:97846790-97846840	Hela-S3	cervix:	n/a
29	chr7:97857492-97857542	HMEC	breast:	n/a
30	chr7:97847054-97847104	ECC-1	luminal epithelium:	n/a
31	chr7:97852022-97852072	AoSMC	blood vessel:	n/a
32	chr7:97846988-97847038	HRE	kidney:	n/a
33	chr7:97851854-97851904	NHDF-neo	bronchial:	n/a
34	chr7:97851854-97851904	A549	lung:	n/a
35	chr7:97857492-97857542	NHDF-neo	bronchial:	n/a
36	chr7:97857971-97858021	AG04450	lung:	fetal
37	chr7:97852022-97852072	GM06990	blood:	n/a
38	chr7:97857938-97857988	SK-N-SH_RA	brain:	n/a
39	chr7:97851854-97851904	ECC-1	luminal epithelium:	n/a
40	chr7:97852022-97852072	IMR90	lung:	fetal
41	chr7:97857938-97857988	GM19239	blood:	n/a
42	chr7:97857647-97857697	IMR90	lung:	fetal
43	chr7:97846988-97847038	ProgFib	skin:	n/a
44	chr7:97847111-97847161	HRPEpiC	eye:	n/a
45	chr7:97857989-97858039	NH-A	brain:	n/a
46	chr7:97857938-97857988	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:97846790-97846840	MCF-7	breast:	n/a
48	chr7:97846790-97846840	SK-N-SH_RA	brain:	n/a
49	chr7:97857356-97857406	AoSMC	blood vessel:	n/a
50	chr7:97846790-97846840	HCPEpiC	choroid plexus:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97845652..97847962-chr7:97851352..97854034,2	MCF-7	breast:
2	chr7:97840601..97843525-chr7:97854047..97856792,2	MCF-7	breast:
3	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
4	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
5	chr7:97840173..97842487-chr7:97845725..97848039,2	MCF-7	breast:
6	chr7:97845652..97847962-chr7:97851352..97854034,2	MCF-7	breast:
7	chr7:97736018..97736542-chr7:97859141..97859647,2	K562	blood:
8	chr7:97844651..97846802-chr7:97859229..97862130,2	MCF-7	breast:
9	chr7:97850503..97852580-chr7:97856044..97857561,2	MCF-7	breast:
10	chr7:97843013..97845825-chr7:97853837..97855430,2	MCF-7	breast:
11	chr7:97854372..97856436-chr7:97905266..97907266,2	MCF-7	breast:
12	chr7:97847018..97848537-chr7:97878984..97881844,2	K562	blood:
13	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
14	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
15	chr7:97844672..97846998-chr7:97849549..97852989,3	K562	blood:
16	chr7:97846624..97850033-chr7:97850682..97852457,3	MCF-7	breast:
17	chr7:97840856..97842377-chr7:97845637..97848224,2	MCF-7	breast:
18	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
19	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
20	chr7:97849669..97852515-chr7:97854128..97855997,2	MCF-7	breast:
21	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
22	chr7:97844457..97846470-chr7:97865336..97867376,2	MCF-7	breast:
23	chr7:97846624..97850033-chr7:97850682..97852457,3	MCF-7	breast:
24	chr7:97851992..97854043-chr7:98027877..98030619,2	K562	blood:
25	chr7:97848875..97850795-chr7:97850910..97852902,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAIAP2L1.1-1	chr7:97855904-97856081	NONHSAT122183

No data

Variant related genes	Relation type
TECPR1	TF binding region
TECPR1	CpG island
ENSG00000006453	chromatin interactions
ENSG00000180535	chromatin interactions
ENSG00000164713	chromatin interactions
ENSG00000164715	chromatin interactions
ENSG00000205356	chromatin interactions

Extended variants
information (count: 642 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74672857	chr7:97846435-97846436	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
2	rs551232399	chr7:97846441-97846442	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs180891863	chr7:97846471-97846472	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs184521770	chr7:97846475-97846476	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551878758	chr7:97846477-97846478	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs570389526	chr7:97846487-97846488	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188494392	chr7:97846501-97846502	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552996034	chr7:97846509-97846510	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs567846256	chr7:97846538-97846539	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs532884774	chr7:97846544-97846545	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs535248783	chr7:97846564-97846565	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs118149966	chr7:97846569-97846570	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs575178302	chr7:97846618-97846619	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546036719	chr7:97846656-97846657	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs557770686	chr7:97846660-97846661	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373837555	chr7:97846673-97846674	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs540284492	chr7:97846677-97846678	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs562148558	chr7:97846693-97846694	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs35234068	chr7:97846713-97846714	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs367911984	chr7:97846734-97846735	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200095183	chr7:97846742-97846743	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538822682	chr7:97846746-97846747	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs375114491	chr7:97846749-97846750	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs533374019	chr7:97846766-97846767	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201224382	chr7:97846804-97846805	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs536426310	chr7:97846814-97846815	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143399165	chr7:97846831-97846832	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs372785614	chr7:97846834-97846835	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs199716089	chr7:97846848-97846849	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546216330	chr7:97846857-97846858	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs35432830	chr7:97846859-97846860	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567809566	chr7:97846907-97846908	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs535213443	chr7:97846918-97846919	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375518406	chr7:97846930-97846931	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116762009	chr7:97846936-97846937	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs367726993	chr7:97846988-97846989	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs376322900	chr7:97846989-97846990	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs371210063	chr7:97846990-97846991	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374994151	chr7:97846991-97846992	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539277605	chr7:97846998-97846999	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs142244449	chr7:97847007-97847008	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs573089891	chr7:97847018-97847019	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs372020510	chr7:97847025-97847026	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs376435004	chr7:97847039-97847040	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs2279676	chr7:97847040-97847041	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs574174338	chr7:97847042-97847043	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs544679303	chr7:97847045-97847046	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs373953014	chr7:97847051-97847052	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs562976025	chr7:97847077-97847078	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs144621652	chr7:97847078-97847079	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97823000-97851000	Weak transcription	HSMMtube	muscle
2	chr7:97825200-97851000	Weak transcription	Fetal Lung	lung
3	chr7:97836000-97851000	Weak transcription	NHLF	lung
4	chr7:97836600-97847200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr7:97836800-97857200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:97837000-97846600	Weak transcription	Dnd41	blood
7	chr7:97839200-97851000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:97840200-97847000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr7:97840200-97847200	Weak transcription	Brain Anterior Caudate	brain
10	chr7:97840200-97847200	Weak transcription	Brain Substantia Nigra	brain
11	chr7:97840200-97851000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:97840400-97847000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr7:97840400-97852800	Weak transcription	Brain Angular Gyrus	brain
14	chr7:97841000-97847200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:97841000-97858600	Weak transcription	Psoas Muscle	Psoas
16	chr7:97841200-97850600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:97841200-97850800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:97841200-97850800	Weak transcription	Osteobl	bone
19	chr7:97841200-97852200	Weak transcription	A549	lung
20	chr7:97841200-97867800	Weak transcription	HUVEC	blood vessel
21	chr7:97841200-97880200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:97841400-97846600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:97841400-97847000	Weak transcription	Primary T cells from cord blood	blood
24	chr7:97841400-97847200	Weak transcription	Primary B cells from cord blood	blood
25	chr7:97841400-97850600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr7:97841400-97858600	Weak transcription	NH-A	brain
27	chr7:97841400-97866200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:97841400-97879400	Weak transcription	Fetal Brain Male	brain
29	chr7:97841400-97880200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr7:97841600-97847000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:97841600-97847000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:97841600-97847200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr7:97841600-97851000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr7:97841600-97853800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:97841800-97850600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr7:97841800-97867400	Weak transcription	Rectal Smooth Muscle	rectum
37	chr7:97842200-97868400	Weak transcription	Colon Smooth Muscle	Colon
38	chr7:97842600-97850600	Weak transcription	Stomach Smooth Muscle	stomach
39	chr7:97842800-97847200	Weak transcription	HepG2	liver
40	chr7:97843200-97847000	Weak transcription	GM12878-XiMat	blood
41	chr7:97843200-97847400	Weak transcription	Duodenum Mucosa	Duodenum
42	chr7:97843400-97847400	Strong transcription	Brain Germinal Matrix	brain
43	chr7:97843400-97850800	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:97843400-97855000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:97843800-97847200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr7:97843800-97847600	Strong transcription	Fetal Stomach	stomach
47	chr7:97843800-97857000	Weak transcription	Right Atrium	heart
48	chr7:97844000-97847200	Strong transcription	Fetal Brain Female	brain
49	chr7:97844200-97846600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr7:97844400-97847000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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