Variant report

Variant	nsv606044
Chromosome Location	chr7:7652372-7727101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1733)
CpG islands
(count:978)
Chromatin interactive
region (count:83)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1733 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7717765-7718021	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:7721171-7721501	K562	blood:	n/a	n/a
3	ARID3A	chr7:7682423-7682622	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:7679656-7680761	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:7656955-7657594	K562	blood:	n/a	n/a
6	ARID3A	chr7:7687281-7687550	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:7679666-7680704	K562	blood:	n/a	n/a
8	ARID3A	chr7:7702363-7702392	K562	blood:	n/a	n/a
9	ARID3A	chr7:7721181-7721479	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:7653637-7654388	K562	blood:	n/a	n/a
11	ARID3A	chr7:7690460-7690804	HepG2	liver:	n/a	n/a
12	ATF1	chr7:7704145-7704243	K562	blood:	n/a	n/a
13	ATF1	chr7:7679604-7680916	K562	blood:	n/a	n/a
14	ATF1	chr7:7693274-7693486	K562	blood:	n/a	n/a
15	ATF1	chr7:7657221-7657576	K562	blood:	n/a	n/a
16	ATF2	chr7:7679409-7680893	GM12878	blood:	n/a	chr7:7679688-7679695
17	ATF2	chr7:7679498-7680900	GM12878	blood:	n/a	chr7:7679688-7679695
18	ATF2	chr7:7679724-7680648	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr7:7679941-7680312	K562	blood:	n/a	n/a
20	ATF3	chr7:7679742-7680659	A549	lung:	n/a	n/a
21	BACH1	chr7:7680074-7680222	K562	blood:	n/a	n/a
22	BACH1	chr7:7679962-7681248	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:7703364-7703366	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:7684942-7684999	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr7:7680230-7680818	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:7680262-7680737	GM12878	blood:	n/a	n/a
27	BCL3	chr7:7680266-7680826	A549	lung:	n/a	n/a
28	BCL3	chr7:7679704-7680384	A549	lung:	n/a	chr7:7680243-7680252
29	BCL3	chr7:7659653-7659874	GM12878	blood:	n/a	n/a
30	BCLAF1	chr7:7679757-7680849	GM12878	blood:	n/a	chr7:7680243-7680252
31	BCLAF1	chr7:7679320-7681168	GM12878	blood:	n/a	chr7:7680243-7680252
32	BHLHE40	chr7:7679913-7680810	HepG2	liver:	n/a	n/a
33	BHLHE40	chr7:7687158-7687709	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:7693238-7693371	K562	blood:	n/a	n/a
35	BHLHE40	chr7:7687220-7687491	HepG2	liver:	n/a	n/a
36	BHLHE40	chr7:7687280-7687428	K562	blood:	n/a	n/a
37	BHLHE40	chr7:7679708-7681227	K562	blood:	n/a	n/a
38	BHLHE40	chr7:7721000-7721346	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:7679193-7679237	K562	blood:	n/a	n/a
40	BHLHE40	chr7:7679570-7681170	GM12878	blood:	n/a	n/a
41	BRCA1	chr7:7679880-7679988	HepG2	liver:	n/a	n/a
42	BRCA1	chr7:7720963-7720964	GM12878	blood:	n/a	n/a
43	BRCA1	chr7:7680053-7680750	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr7:7679946-7680833	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:7679883-7680984	GM12878	blood:	n/a	n/a
46	BRCA1	chr7:7680273-7680704	HepG2	liver:	n/a	n/a
47	CBX3	chr7:7681630-7682044	K562	blood:	n/a	n/a
48	CBX3	chr7:7679847-7680889	K562	blood:	n/a	n/a
49	CBX3	chr7:7679845-7680342	K562	blood:	n/a	n/a
50	CBX3	chr7:7717456-7717943	K562	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7726202-7726252	HCF	heart:	n/a
2	chr7:7680678-7680728	HL-60	blood:	n/a
3	chr7:7726202-7726252	HCF	heart:	n/a
4	chr7:7680678-7680728	HL-60	blood:	n/a
5	chr7:7676611-7676661	GM12891	blood:	n/a
6	chr7:7681162-7681212	K562	blood:	n/a
7	chr7:7681016-7681066	NHDF-neo	bronchial:	n/a
8	chr7:7680871-7680921	IMR90	lung:	fetal
9	chr7:7680678-7680728	RPTEC	kidney:	n/a
10	chr7:7678631-7678681	SK-N-SH	brain:	n/a
11	chr7:7680871-7680921	HMEC	breast:	n/a
12	chr7:7680361-7680411	MCF10A-Er-Src	breast:	n/a
13	chr7:7681162-7681212	Jurkat	blood:	n/a
14	chr7:7680075-7680125	GM12892	blood:	n/a
15	chr7:7680678-7680728	HEK293	kidney:	embryo
16	chr7:7680871-7680921	HUVEC	blood vessel:	n/a
17	chr7:7682912-7682962	AoSMC	blood vessel:	n/a
18	chr7:7680321-7680371	GM06990	blood:	n/a
19	chr7:7679762-7679812	IMR90	lung:	fetal
20	chr7:7680321-7680371	HRCEpiC	kidney:	n/a
21	chr7:7679762-7679812	HCF	heart:	n/a
22	chr7:7680871-7680921	HCT-116	colon:	n/a
23	chr7:7680871-7680921	NB4	blood:	n/a
24	chr7:7680321-7680371	SK-N-SH_RA	brain:	n/a
25	chr7:7676611-7676661	HEK293	kidney:	embryo
26	chr7:7680075-7680125	HEEpiC	esophagus:	n/a
27	chr7:7679762-7679812	HIPEpiC	eye:	n/a
28	chr7:7711168-7711218	K562	blood:	n/a
29	chr7:7680086-7680136	HCPEpiC	choroid plexus:	n/a
30	chr7:7679762-7679812	MCF10A-Er-Src	breast:	n/a
31	chr7:7680678-7680728	HepG2	liver:	n/a
32	chr7:7682912-7682962	GM06990	blood:	n/a
33	chr7:7680075-7680125	BJ	skin:	n/a
34	chr7:7680020-7680070	NT2-D1	testis:	n/a
35	chr7:7726202-7726252	SKMC	muscle:	n/a
36	chr7:7680020-7680070	HRPEpiC	eye:	n/a
37	chr7:7680020-7680070	LNCaP	prostate:	n/a
38	chr7:7711168-7711218	HepG2	liver:	n/a
39	chr7:7679762-7679812	K562	blood:	n/a
40	chr7:7679762-7679812	HEK293	kidney:	embryo
41	chr7:7680086-7680136	NT2-D1	testis:	n/a
42	chr7:7680678-7680728	MCF-7	breast:	n/a
43	chr7:7726202-7726252	GM06990	blood:	n/a
44	chr7:7726202-7726252	NHBE	bronchial:	n/a
45	chr7:7676611-7676661	PrEC	prostate:	n/a
46	chr7:7676611-7676661	HEEpiC	esophagus:	n/a
47	chr7:7678631-7678681	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:7680075-7680125	HL-60	blood:	n/a
49	chr7:7680871-7680921	T-47D	breast:	n/a
50	chr7:7680075-7680125	NHBE	bronchial:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:7726990..7730835-chr7:7733488..7736848,3	K562	blood:
2	chr7:7673907..7678610-chr7:7678691..7681851,6	MCF-7	breast:
3	chr7:7680700..7683473-chr7:7685626..7688056,2	MCF-7	breast:
4	chr7:7708519..7710790-chr7:7711847..7714046,2	K562	blood:
5	chr2:240322904..240323542-chr7:7680267..7680816,2	Hela-S3	cervix:
6	chr7:7704790..7707554-chr7:7715010..7717465,2	K562	blood:
7	chr11:64018519..64019489-chr7:7679437..7680045,2	Hela-S3	cervix:
8	chr7:7623467..7625147-chr7:7680756..7682414,2	K562	blood:
9	chr7:7645252..7648963-chr7:7651944..7654788,5	K562	blood:
10	chr15:41165970..41166558-chr7:7679740..7680262,2	Hela-S3	cervix:
11	chr7:7679025..7680643-chr7:7683865..7686484,2	MCF-7	breast:
12	chr7:7658111..7660487-chr7:7677718..7679427,3	K562	blood:
13	chr7:7683722..7685849-chr7:7692076..7694562,2	MCF-7	breast:
14	chr17:41466087..41467053-chr7:7679547..7680423,2	Hela-S3	cervix:
15	chr7:7654403..7655904-chr7:7677926..7679553,2	K562	blood:
16	chr7:7676999..7684981-chr7:7684990..7693882,16	K562	blood:
17	chr7:7679018..7681584-chr7:8008760..8011156,4	K562	blood:
18	chr7:7648154..7650779-chr7:7652193..7654912,3	K562	blood:
19	chr7:7605830..7608267-chr7:7679102..7681869,5	MCF-7	breast:
20	chr7:7663362..7666136-chr7:7675312..7676994,2	MCF-7	breast:
21	chr7:7678479..7681346-chr7:8300009..8302111,2	K562	blood:
22	chr7:7704790..7707554-chr7:7715010..7717465,2	K562	blood:
23	chr7:7720780..7722829-chr7:8008432..8010921,2	MCF-7	breast:
24	chr7:7679155..7682446-chr7:7688919..7692688,4	MCF-7	breast:
25	chr7:7674801..7676946-chr7:7679049..7682761,4	K562	blood:
26	chr7:7713254..7715065-chr7:7752185..7753849,2	K562	blood:
27	chr7:7685666..7688418-chr7:7688824..7691434,2	K562	blood:
28	chr7:7675114..7677111-chr7:8008859..8010414,2	K562	blood:
29	chr7:7710276..7712409-chr7:7714485..7717060,3	MCF-7	breast:
30	chr7:7672448..7678421-chr7:7678475..7681557,8	K562	blood:
31	chr17:74732854..74733643-chr7:7679556..7680144,2	NB4	blood:
32	chr7:7721232..7721744-chr7:8075592..8076157,2	MCF-7	breast:
33	chr7:7726921..7729917-chr7:7734737..7737606,4	K562	blood:
34	chr7:7678621..7681872-chr7:7690488..7692343,3	MCF-7	breast:
35	chr7:7603046..7608569-chr7:7677123..7682101,8	MCF-7	breast:
36	chr2:190649071..190649611-chr7:7679917..7680683,2	Hela-S3	cervix:
37	chr7:7675254..7676808-chr7:7682969..7685532,2	MCF-7	breast:
38	chr7:7663362..7666136-chr7:7675312..7676994,2	MCF-7	breast:
39	chr7:7680700..7683473-chr7:7685626..7688056,2	MCF-7	breast:
40	chr7:7673420..7676020-chr7:7676978..7678609,2	MCF-7	breast:
41	chr7:7650609..7654175-chr7:7655062..7657334,4	K562	blood:
42	chr7:7661481..7665380-chr7:7678984..7681458,3	K562	blood:
43	chr7:7658111..7660487-chr7:7677718..7679427,3	K562	blood:
44	chr7:7680697..7682834-chr7:8264362..8267648,3	K562	blood:
45	chr7:7673907..7678610-chr7:7678691..7681851,6	MCF-7	breast:
46	chr7:7606336..7608095-chr7:7669246..7672154,2	MCF-7	breast:
47	chr11:65190262..65191059-chr7:7679930..7680646,2	Hela-S3	cervix:
48	chr12:52447172..52448025-chr7:7679986..7680652,2	Hela-S3	cervix:
49	chr7:7655938..7658869-chr7:7680457..7682421,2	K562	blood:
50	chr7:7708519..7710790-chr7:7711847..7714046,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL28A1-3	chr7:7678210-7678775	NONHSAT119122
2	lnc-COL28A1-3	chr7:7680354-7680580	NONHSAT119122
3	lnc-MIOS-3	chr7:7659503-7660174	ENSG00000272745.1

No data

Variant related genes	Relation type
ENSG00000272745	TF binding region
RPA3-AS1	TF binding region
RPA3	TF binding region
ENSG00000272745	CpG island
RPA3-AS1	CpG island
RPA3	CpG island
ENSG00000112308	chromatin interactions
ENSG00000003147	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000164654	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000128699	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000229970	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000222020	chromatin interactions
ENSG00000104140	chromatin interactions
ENSG00000068024	chromatin interactions
ENSG00000219545	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000181938	chromatin interactions
ENSG00000106415	chromatin interactions
ENSG00000244239	chromatin interactions
ENSG00000149782	chromatin interactions
ENSG00000064933	chromatin interactions
ENSG00000233108	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000106399	chromatin interactions
ENSG00000272745	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000272894	chromatin interactions

Extended variants
information (count: 3460 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3460 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7787734	chr7:7652372-7652373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561678479	chr7:7652380-7652381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554044103	chr7:7652385-7652386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566379354	chr7:7652394-7652395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs180721241	chr7:7652562-7652563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558007531	chr7:7652568-7652569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185159179	chr7:7652569-7652570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189926080	chr7:7652581-7652582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555450951	chr7:7652597-7652598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs117514058	chr7:7652609-7652610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183047795	chr7:7652624-7652625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138564244	chr7:7652720-7652721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541245046	chr7:7652784-7652785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559252434	chr7:7652945-7652946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7801182	chr7:7652977-7652978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs186930421	chr7:7653040-7653041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563563022	chr7:7653065-7653066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7801325	chr7:7653076-7653077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560362908	chr7:7653180-7653181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552468815	chr7:7653187-7653188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549858625	chr7:7653233-7653234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568561969	chr7:7653246-7653247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146742486	chr7:7653271-7653272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547853795	chr7:7653282-7653283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191775322	chr7:7653301-7653302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561011800	chr7:7653333-7653334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571111758	chr7:7653382-7653383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537883632	chr7:7653435-7653436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183980377	chr7:7653465-7653466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147692760	chr7:7653475-7653476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55670462	chr7:7653479-7653480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367565663	chr7:7653486-7653487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569976359	chr7:7653496-7653497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188925829	chr7:7653512-7653513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192573107	chr7:7653572-7653573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574877813	chr7:7653582-7653583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182172491	chr7:7653590-7653591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10250880	chr7:7653628-7653629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553026775	chr7:7653644-7653645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554262731	chr7:7653740-7653741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577950997	chr7:7653770-7653771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10251012	chr7:7653776-7653777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs55769451	chr7:7653789-7653790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs186819778	chr7:7653888-7653889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372711323	chr7:7653971-7653972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72432716	chr7:7653972-7653973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs202138182	chr7:7653978-7653979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200171213	chr7:7653979-7653980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117433286	chr7:7653981-7653982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191741122	chr7:7654009-7654010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	17229543	CNVD
Ovarian cancer	21781307	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1599 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7609600-7652600	Weak transcription	Fetal Brain Male	brain
2	chr7:7610600-7654400	Weak transcription	Gastric	stomach
3	chr7:7611200-7652400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr7:7621600-7656400	Weak transcription	Aorta	Aorta
5	chr7:7637600-7658000	Weak transcription	Fetal Intestine Small	intestine
6	chr7:7639600-7653800	Weak transcription	Fetal Heart	heart
7	chr7:7639600-7657200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr7:7639800-7674600	Weak transcription	A549	lung
9	chr7:7647000-7654000	Weak transcription	Left Ventricle	heart
10	chr7:7647000-7656800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr7:7647200-7652400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr7:7647200-7656400	Weak transcription	Dnd41	blood
13	chr7:7647600-7653800	Weak transcription	K562	blood
14	chr7:7647800-7652600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr7:7647800-7655600	Weak transcription	GM12878-XiMat	blood
16	chr7:7647800-7657600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:7648000-7656600	Weak transcription	Primary T cells from cord blood	blood
18	chr7:7648600-7652400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:7648600-7660200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:7649000-7679000	Weak transcription	HSMM	muscle
21	chr7:7649200-7652600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr7:7649200-7653000	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr7:7649200-7653000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:7649200-7654200	Weak transcription	Adipose Nuclei	Adipose
25	chr7:7649200-7657600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr7:7649800-7657800	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr7:7650200-7657200	Weak transcription	Primary B cells from cord blood	blood
28	chr7:7650800-7652800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:7651200-7653000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr7:7653800-7654000	Enhancers	Fetal Heart	heart
31	chr7:7653800-7656000	Enhancers	K562	blood
32	chr7:7656000-7656400	Weak transcription	K562	blood
33	chr7:7656400-7656800	Enhancers	Dnd41	blood
34	chr7:7656400-7656800	Enhancers	K562	blood
35	chr7:7656600-7657800	Enhancers	Primary T cells from cord blood	blood
36	chr7:7656800-7657000	Flanking Active TSS	Dnd41	blood
37	chr7:7656800-7657400	Flanking Active TSS	K562	blood
38	chr7:7657000-7657200	Enhancers	Dnd41	blood
39	chr7:7657200-7657400	Flanking Active TSS	Dnd41	blood
40	chr7:7657200-7657800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr7:7657400-7658400	Enhancers	Dnd41	blood
42	chr7:7657400-7658400	Enhancers	K562	blood
43	chr7:7657800-7658000	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr7:7658000-7658400	Enhancers	Fetal Intestine Small	intestine
45	chr7:7659600-7659800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr7:7660200-7660800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:7662800-7663200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr7:7665400-7665600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr7:7669000-7679000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:7670800-7674800	Weak transcription	Primary T cells from cord blood	blood

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