Variant report

Variant	nsv525934
Chromosome Location	chr7:97853184-97866291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:368)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97855510-97855782	HepG2	liver:	n/a	n/a
2	CCNT2	chr7:97857856-97857921	K562	blood:	n/a	n/a
3	CEBPB	chr7:97857410-97857839	MCF-7	breast:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
4	CEBPB	chr7:97857541-97857759	H1-hESC	embryonic stem cell:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
5	CEBPB	chr7:97857468-97857829	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
6	CEBPB	chr7:97857558-97857722	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
7	CEBPB	chr7:97857481-97857783	IMR90	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
8	CEBPB	chr7:97857458-97857785	A549	lung:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
9	CEBPB	chr7:97857468-97857755	K562	blood:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
10	CEBPB	chr7:97857460-97857814	HepG2	liver:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
11	CEBPB	chr7:97857556-97857798	Hela-S3	cervix:	n/a	chr7:97857633-97857644 chr7:97857634-97857645 chr7:97857635-97857644 chr7:97857633-97857646
12	CTCF	chr7:97863860-97864010	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr7:97859540-97859690	GM12873	blood:	n/a	n/a
14	CTCF	chr7:97859598-97859710	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr7:97863820-97863970	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr7:97863860-97864010	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr7:97853955-97854015	H1-hESC	embryonic stem cell:	n/a	chr7:97853977-97853986
18	CTCF	chr7:97859560-97859710	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr7:97859593-97859672	MCF-7	breast:	n/a	n/a
20	CTCF	chr7:97859600-97859750	GM12864	blood:	n/a	n/a
21	CTCF	chr7:97863740-97863890	NHLF	lung:	n/a	n/a
22	CTCF	chr7:97863800-97863950	HPF	lung:	n/a	n/a
23	CTCF	chr7:97863880-97864030	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr7:97863880-97864030	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:97859560-97859710	A549	lung:	n/a	n/a
26	CTCF	chr7:97859562-97859687	K562	blood:	n/a	n/a
27	CTCF	chr7:97863860-97864010	AG09319	gingival:	n/a	n/a
28	CTCF	chr7:97863840-97863990	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr7:97863800-97863950	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr7:97859633-97859670	GM19239	blood:	n/a	n/a
31	CTCF	chr7:97859560-97859710	GM12870	blood:	n/a	n/a
32	CTCF	chr7:97859476-97859741	K562	blood:	n/a	n/a
33	CTCF	chr7:97863840-97863990	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:97865703-97865756	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr7:97863840-97863990	AG10803	skin:	n/a	n/a
36	CTCF	chr7:97863880-97864030	HVMF	connective:	n/a	n/a
37	CTCF	chr7:97859540-97859690	GM12868	blood:	n/a	n/a
38	CTCF	chr7:97859559-97859657	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr7:97863840-97863990	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr7:97859505-97859705	GM12878	blood:	n/a	n/a
41	CTCF	chr7:97863885-97864116	IMR90	lung:	n/a	n/a
42	CTCF	chr7:97863860-97864010	WI-38	lung:	n/a	n/a
43	CTCF	chr7:97859566-97859694	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:97859611-97859660	K562	blood:	n/a	n/a
45	CTCF	chr7:97863840-97863990	BJ	skin:	n/a	n/a
46	CTCF	chr7:97863840-97863990	HCFaa	heart:	n/a	n/a
47	CTCF	chr7:97863860-97864010	HPF	lung:	n/a	n/a
48	CTCF	chr7:97859540-97859690	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr7:97859595-97859662	HepG2	liver:	n/a	n/a
50	CTCF	chr7:97863820-97863970	HCT-116	colon:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97857971-97858021	HCPEpiC	choroid plexus:	n/a
2	chr7:97857492-97857542	HEEpiC	esophagus:	n/a
3	chr7:97857971-97858021	HCPEpiC	choroid plexus:	n/a
4	chr7:97857492-97857542	HEEpiC	esophagus:	n/a
5	chr7:97857989-97858039	PrEC	prostate:	n/a
6	chr7:97857971-97858021	GM19239	blood:	n/a
7	chr7:97857971-97858021	GM12892	blood:	n/a
8	chr7:97857938-97857988	GM06990	blood:	n/a
9	chr7:97857971-97858021	GM06990	blood:	n/a
10	chr7:97857989-97858039	AG09319	gingival:	n/a
11	chr7:97857989-97858039	ProgFib	skin:	n/a
12	chr7:97857356-97857406	HNPCEpiC	eye:	n/a
13	chr7:97857989-97858039	SK-N-MC	brain:	n/a
14	chr7:97857989-97858039	SK-N-SH	brain:	n/a
15	chr7:97857938-97857988	CMK	blood:	n/a
16	chr7:97857356-97857406	PFSK-1	brain:	n/a
17	chr7:97857989-97858039	HEEpiC	esophagus:	n/a
18	chr7:97857971-97858021	A549	lung:	n/a
19	chr7:97857647-97857697	AG10803	skin:	n/a
20	chr7:97857647-97857697	NB4	blood:	n/a
21	chr7:97857989-97858039	K562	blood:	n/a
22	chr7:97857647-97857697	SAEC	small airway:	n/a
23	chr7:97857938-97857988	HMEC	breast:	n/a
24	chr7:97857647-97857697	HRPEpiC	eye:	n/a
25	chr7:97857989-97858039	SAEC	small airway:	n/a
26	chr7:97857971-97858021	K562	blood:	n/a
27	chr7:97857492-97857542	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:97857989-97858039	RPTEC	kidney:	n/a
29	chr7:97857356-97857406	A549	lung:	n/a
30	chr7:97857938-97857988	IMR90	lung:	fetal
31	chr7:97857356-97857406	GM06990	blood:	n/a
32	chr7:97857492-97857542	IMR90	lung:	fetal
33	chr7:97857356-97857406	LNCaP	prostate:	n/a
34	chr7:97857989-97858039	HNPCEpiC	eye:	n/a
35	chr7:97857647-97857697	ProgFib	skin:	n/a
36	chr7:97857356-97857406	Hepatocyte	liver:	n/a
37	chr7:97857938-97857988	HAEpiC	amniotic membrane:	n/a
38	chr7:97857989-97858039	HRPEpiC	eye:	n/a
39	chr7:97857989-97858039	Jurkat	blood:	n/a
40	chr7:97857492-97857542	AG04449	skin:	fetal
41	chr7:97857938-97857988	HCPEpiC	choroid plexus:	n/a
42	chr7:97857647-97857697	GM06990	blood:	n/a
43	chr7:97857356-97857406	HCPEpiC	choroid plexus:	n/a
44	chr7:97857971-97858021	ovcar-3	ovarian:	n/a
45	chr7:97857647-97857697	PANC-1	pancreas:	n/a
46	chr7:97857647-97857697	AG04450	lung:	fetal
47	chr7:97857938-97857988	AG04450	lung:	fetal
48	chr7:97857356-97857406	MCF10A-Er-Src	breast:	n/a
49	chr7:97857492-97857542	AG04450	lung:	fetal
50	chr7:97857647-97857697	SKMC	muscle:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
2	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
3	chr7:97855900..97859430-chr7:97859536..97863597,5	K562	blood:
4	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
5	chr7:97860162..97861679-chr7:97865709..97867211,2	K562	blood:
6	chr7:97859627..97861679-chr7:97864267..97867211,3	K562	blood:
7	chr7:97840601..97843525-chr7:97854047..97856792,2	MCF-7	breast:
8	chr7:97864661..97867509-chr7:97913185..97914838,2	K562	blood:
9	chr7:97850503..97852580-chr7:97856044..97857561,2	MCF-7	breast:
10	chr7:97852038..97854221-chr7:97858720..97861626,2	K562	blood:
11	chr7:97863932..97867672-chr7:97911936..97914933,4	K562	blood:
12	chr7:97849669..97852515-chr7:97854128..97855997,2	MCF-7	breast:
13	chr7:97851992..97854043-chr7:98027877..98030619,2	K562	blood:
14	chr7:97736018..97736542-chr7:97859141..97859647,2	K562	blood:
15	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
16	chr7:97844457..97846470-chr7:97865336..97867376,2	MCF-7	breast:
17	chr7:97845652..97847962-chr7:97851352..97854034,2	MCF-7	breast:
18	chr7:97856853..97859971-chr7:97865587..97869015,3	MCF-7	breast:
19	chr7:97854372..97856436-chr7:97905266..97907266,2	MCF-7	breast:
20	chr7:97852333..97858295-chr7:97859641..97865309,7	MCF-7	breast:
21	chr7:97842812..97845120-chr7:97865672..97868033,2	K562	blood:
22	chr7:97843013..97845825-chr7:97853837..97855430,2	MCF-7	breast:

(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
ENSG00000205356	chromatin interactions
ENSG00000180535	chromatin interactions
ENSG00000164715	chromatin interactions

Extended variants
information (count: 667 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3816943	chr7:97853184-97853185	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562624707	chr7:97853205-97853206	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs532960521	chr7:97853213-97853214	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs551634899	chr7:97853225-97853226	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs566760976	chr7:97853237-97853238	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs527630090	chr7:97853275-97853276	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs35446950	chr7:97853281-97853282	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs34377813	chr7:97853286-97853287	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs13231773	chr7:97853309-97853310	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs567505925	chr7:97853313-97853314	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs527962871	chr7:97853333-97853334	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs112359285	chr7:97853351-97853352	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs564655020	chr7:97853388-97853389	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs538840255	chr7:97853408-97853409	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs553991997	chr7:97853424-97853425	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs190538287	chr7:97853451-97853452	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs60997612	chr7:97853489-97853490	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs554858704	chr7:97853516-97853517	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs573527669	chr7:97853583-97853584	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs532659027	chr7:97853588-97853589	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs145645240	chr7:97853590-97853591	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs544222299	chr7:97853593-97853594	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs562426524	chr7:97853630-97853631	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs533088293	chr7:97853649-97853650	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs56884531	chr7:97853682-97853683	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs182198488	chr7:97853683-97853684	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs550238172	chr7:97853713-97853714	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs2291747	chr7:97853795-97853796	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs529225903	chr7:97853803-97853804	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs561266179	chr7:97853828-97853829	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs531596145	chr7:97853844-97853845	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs2291746	chr7:97853845-97853846	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs139883403	chr7:97853850-97853851	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs566443331	chr7:97853875-97853876	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs538700970	chr7:97853876-97853877	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs537774745	chr7:97853879-97853880	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs565901311	chr7:97853910-97853911	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs185946352	chr7:97853925-97853926	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs554941601	chr7:97853953-97853954	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs576707180	chr7:97853960-97853961	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs79279492	chr7:97854015-97854016	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs145388001	chr7:97854085-97854086	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs369237240	chr7:97854089-97854090	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs373744345	chr7:97854160-97854161	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189881169	chr7:97854233-97854234	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs144232728	chr7:97854269-97854270	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560302681	chr7:97854295-97854296	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs370602624	chr7:97854301-97854302	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373463840	chr7:97854308-97854309	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs376380225	chr7:97854343-97854344	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97836800-97857200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:97841000-97858600	Weak transcription	Psoas Muscle	Psoas
3	chr7:97841200-97867800	Weak transcription	HUVEC	blood vessel
4	chr7:97841200-97880200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:97841400-97858600	Weak transcription	NH-A	brain
6	chr7:97841400-97866200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr7:97841400-97879400	Weak transcription	Fetal Brain Male	brain
8	chr7:97841400-97880200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr7:97841600-97853800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:97841800-97867400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:97842200-97868400	Weak transcription	Colon Smooth Muscle	Colon
12	chr7:97843400-97855000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:97843800-97857000	Weak transcription	Right Atrium	heart
14	chr7:97845200-97877400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr7:97846800-97856400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:97848000-97857600	Weak transcription	Stomach Mucosa	stomach
17	chr7:97848000-97877600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr7:97848000-97880600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:97848600-97873200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr7:97848800-97855200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:97849000-97864600	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr7:97849200-97857800	Strong transcription	Fetal Muscle Leg	muscle
23	chr7:97849400-97863400	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr7:97849800-97858000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr7:97850000-97871800	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr7:97850000-97878000	Strong transcription	Fetal Stomach	stomach
27	chr7:97850200-97858200	Strong transcription	Liver	Liver
28	chr7:97850200-97874400	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr7:97850200-97875400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr7:97850400-97872800	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr7:97850400-97878600	Weak transcription	GM12878-XiMat	blood
32	chr7:97850600-97853200	Strong transcription	Stomach Smooth Muscle	stomach
33	chr7:97850600-97855400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:97850600-97855600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:97850600-97856200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr7:97850600-97856200	Strong transcription	Brain Germinal Matrix	brain
37	chr7:97850600-97864200	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr7:97850600-97872800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr7:97850600-97874400	Strong transcription	Adipose Nuclei	Adipose
40	chr7:97850600-97875600	Strong transcription	Fetal Brain Female	brain
41	chr7:97850800-97854000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:97850800-97855600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:97850800-97855800	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:97850800-97856000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:97850800-97856000	Strong transcription	Fetal Muscle Trunk	muscle
46	chr7:97850800-97858400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr7:97850800-97860600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:97850800-97863000	Strong transcription	Ovary	ovary
49	chr7:97850800-97863600	Strong transcription	Lung	lung
50	chr7:97850800-97864200	Strong transcription	Fetal Intestine Small	intestine

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