Variant report

Variant	esv1834835
Chromosome Location	chr7:6681006-6695998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:915)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 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	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
2	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
3	BHLHE40	chr7:6685656-6685802	K562	blood:	n/a	n/a
4	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
5	CHD2	chr7:6688733-6688788	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr7:6687900-6688050	HMEC	breast:	n/a	n/a
7	CTCF	chr7:6688006-6688143	MCF-7	breast:	n/a	n/a
8	CTCF	chr7:6685100-6685250	MCF-7	breast:	n/a	n/a
9	CTCF	chr7:6688038-6688147	MCF-7	breast:	n/a	n/a
10	CTCF	chr7:6688074-6688083	MCF-7	breast:	n/a	n/a
11	CTCF	chr7:6687960-6688110	SK-N-SH_RA	brain:	n/a	n/a
12	EGR1	chr7:6682837-6682995	K562	blood:	n/a	chr7:6682938-6682949 chr7:6682936-6682951
13	EGR1	chr7:6682803-6683044	K562	blood:	n/a	chr7:6682938-6682949 chr7:6682936-6682951
14	ELF1	chr7:6693518-6693985	GM12878	blood:	n/a	n/a
15	ELF1	chr7:6694512-6694819	GM12878	blood:	n/a	n/a
16	GABPA	chr7:6693265-6693772	H1-hESC	embryonic stem cell:	n/a	n/a
17	GABPA	chr7:6693871-6694198	H1-hESC	embryonic stem cell:	n/a	n/a
18	HMGN3	chr7:6692437-6692466	K562	blood:	n/a	n/a
19	HNF4A	chr7:6680956-6681244	HepG2	liver:	n/a	chr7:6681157-6681179 chr7:6681112-6681134 chr7:6681065-6681087
20	MYC	chr7:6692304-6692375	MCF-7	breast:	n/a	n/a
21	MYC	chr7:6687405-6687481	MCF-7	breast:	n/a	n/a
22	MYC	chr7:6693497-6693638	MCF-7	breast:	n/a	n/a
23	PAX5	chr7:6692399-6692566	GM12878	blood:	n/a	n/a
24	PAX5	chr7:6693740-6694153	GM12878	blood:	n/a	chr7:6693933-6693952
25	PAX5	chr7:6692282-6692683	GM12891	blood:	n/a	n/a
26	PAX5	chr7:6692292-6692760	GM12878	blood:	n/a	n/a
27	PAX5	chr7:6692302-6692682	GM12878	blood:	n/a	n/a
28	PAX5	chr7:6693543-6694257	GM12878	blood:	n/a	chr7:6693933-6693952
29	PAX5	chr7:6693715-6694061	GM12878	blood:	n/a	chr7:6693933-6693952
30	PAX5	chr7:6693823-6694038	GM12892	blood:	n/a	chr7:6693933-6693952
31	PAX5	chr7:6693717-6694116	GM12891	blood:	n/a	chr7:6693933-6693952
32	PAX5	chr7:6693471-6694164	GM12892	blood:	n/a	chr7:6693933-6693952
33	PAX5	chr7:6692099-6692801	GM12892	blood:	n/a	n/a
34	PAX5	chr7:6692203-6692749	GM12878	blood:	n/a	n/a
35	PBX3	chr7:6693289-6693652	GM12878	blood:	n/a	n/a
36	PBX3	chr7:6693877-6694030	GM12878	blood:	n/a	n/a
37	POLR2A	chr7:6681957-6682757	K562	blood:	n/a	n/a
38	POLR2A	chr7:6686825-6687614	GM12878	blood:	n/a	n/a
39	POLR2A	chr7:6681077-6681504	K562	blood:	n/a	n/a
40	POLR2A	chr7:6686026-6686045	K562	blood:	n/a	n/a
41	POLR2A	chr7:6690660-6690860	K562	blood:	n/a	n/a
42	POLR2A	chr7:6694042-6694952	GM12878	blood:	n/a	n/a
43	POLR2A	chr7:6685736-6685763	K562	blood:	n/a	n/a
44	POLR2A	chr7:6690407-6690409	MCF-7	breast:	n/a	n/a
45	POLR2A	chr7:6690348-6690680	GM12878	blood:	n/a	n/a
46	POLR2A	chr7:6687446-6687508	MCF-7	breast:	n/a	n/a
47	POLR2A	chr7:6682749-6683216	GM12878	blood:	n/a	n/a
48	POLR2A	chr7:6688660-6688773	K562	blood:	n/a	n/a
49	POLR2A	chr7:6694059-6696588	K562	blood:	n/a	n/a
50	POLR2A	chr7:6693936-6693957	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6681379-6681429	BE2_C	brain:	n/a
2	chr7:6693334-6693384	NHDF-neo	bronchial:	n/a
3	chr7:6692445-6692495	HRCEpiC	kidney:	n/a
4	chr7:6690313-6690363	HepG2	liver:	n/a
5	chr7:6695121-6695171	H1-hESC	embryonic stem cell:	embryo
6	chr7:6691949-6691999	IMR90	lung:	fetal
7	chr7:6693838-6693888	PANC-1	pancreas:	n/a
8	chr7:6693334-6693384	SK-N-SH	brain:	n/a
9	chr7:6689218-6689268	HCPEpiC	choroid plexus:	n/a
10	chr7:6694373-6694423	AG09319	gingival:	n/a
11	chr7:6692873-6692923	HEK293	kidney:	embryo
12	chr7:6682784-6682834	ProgFib	skin:	n/a
13	chr7:6682784-6682834	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:6695121-6695171	AG04449	skin:	fetal
15	chr7:6694735-6694785	HMEC	breast:	n/a
16	chr7:6692873-6692923	K562	blood:	n/a
17	chr7:6694373-6694423	GM19239	blood:	n/a
18	chr7:6694735-6694785	HAEpiC	amniotic membrane:	n/a
19	chr7:6695121-6695171	HAEpiC	amniotic membrane:	n/a
20	chr7:6682784-6682834	NT2-D1	testis:	n/a
21	chr7:6694735-6694785	MCF-7	breast:	n/a
22	chr7:6692873-6692923	GM12892	blood:	n/a
23	chr7:6693030-6693080	HAEpiC	amniotic membrane:	n/a
24	chr7:6694373-6694423	GM12892	blood:	n/a
25	chr7:6689218-6689268	BE2_C	brain:	n/a
26	chr7:6681379-6681429	GM12891	blood:	n/a
27	chr7:6681379-6681429	Jurkat	blood:	n/a
28	chr7:6691949-6691999	BJ	skin:	n/a
29	chr7:6693334-6693384	AG04449	skin:	fetal
30	chr7:6689218-6689268	GM12878	blood:	n/a
31	chr7:6693838-6693888	HUVEC	blood vessel:	n/a
32	chr7:6691949-6691999	ECC-1	luminal epithelium:	n/a
33	chr7:6692873-6692923	ovcar-3	ovarian:	n/a
34	chr7:6692873-6692923	AoSMC	blood vessel:	n/a
35	chr7:6689218-6689268	U87	brain:	n/a
36	chr7:6693334-6693384	GM12891	blood:	n/a
37	chr7:6695092-6695142	ovcar-3	ovarian:	n/a
38	chr7:6695121-6695171	HCF	heart:	n/a
39	chr7:6694373-6694423	PFSK-1	brain:	n/a
40	chr7:6693838-6693888	T-47D	breast:	n/a
41	chr7:6694735-6694785	NH-A	brain:	n/a
42	chr7:6694978-6695028	HRE	kidney:	n/a
43	chr7:6692873-6692923	NH-A	brain:	n/a
44	chr7:6693030-6693080	PANC-1	pancreas:	n/a
45	chr7:6691949-6691999	NHBE	bronchial:	n/a
46	chr7:6693334-6693384	SKMC	muscle:	n/a
47	chr7:6695121-6695171	A549	lung:	n/a
48	chr7:6689218-6689268	BJ	skin:	n/a
49	chr7:6693030-6693080	AG04449	skin:	fetal
50	chr7:6689218-6689268	Jurkat	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
2	chr7:6683236..6686038-chr7:6768255..6771021,2	K562	blood:
3	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
4	chr7:6674209..6679608-chr7:6682918..6689628,9	K562	blood:
5	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
6	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
7	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
8	chr7:6669640..6671625-chr7:6687041..6689974,2	MCF-7	breast:
9	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
10	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
11	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
12	chr7:6675427..6681659-chr7:6684293..6688490,10	MCF-7	breast:
13	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
14	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
15	chr7:6681243..6682856-chr7:6746246..6748831,2	K562	blood:
16	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
17	chr7:6687023..6688997-chr7:6745010..6747605,2	K562	blood:
18	chr7:6682551..6684434-chr7:6694308..6696080,2	MCF-7	breast:
19	chr7:6679487..6682483-chr7:6695124..6696654,2	MCF-7	breast:
20	chr7:6672567..6674181-chr7:6688854..6690680,2	K562	blood:
21	chr7:6694849..6698438-chr7:6699530..6702045,3	K562	blood:
22	chr7:6614762..6617092-chr7:6682142..6684739,2	K562	blood:
23	chr7:6680149..6683134-chr7:6689202..6690780,2	K562	blood:
24	chr7:6668677..6671566-chr7:6683216..6685538,2	MCF-7	breast:
25	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
26	chr7:6660564..6662217-chr7:6683757..6686361,2	MCF-7	breast:
27	chr7:6660093..6661828-chr7:6695492..6697100,2	MCF-7	breast:
28	chr7:6627001..6634994-chr7:6673643..6681623,15	MCF-7	breast:
29	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
30	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1

No data

Variant related genes	Relation type
ZNF316	TF binding region
ENSG00000260054	TF binding region
ZNF316	CpG island
ENSG00000260054	CpG island
ENSG00000136247	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000260054	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000205903	chromatin interactions

Extended variants
information (count: 695 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:695 , 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	rs4720680	chr7:6681006-6681007	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553001712	chr7:6681009-6681010	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs377422525	chr7:6681047-6681048	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs192401039	chr7:6681058-6681059	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs539298606	chr7:6681061-6681062	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs142037295	chr7:6681065-6681066	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs576916123	chr7:6681109-6681110	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs575719267	chr7:6681121-6681122	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs182501752	chr7:6681189-6681190	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs12667876	chr7:6681210-6681211	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs572977551	chr7:6681253-6681254	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs117400829	chr7:6681285-6681286	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs564898561	chr7:6681295-6681296	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs532376552	chr7:6681299-6681300	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs544948427	chr7:6681351-6681352	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs576156778	chr7:6681355-6681356	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs563616714	chr7:6681379-6681380	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs146254987	chr7:6681398-6681399	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs77853908	chr7:6681410-6681411	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs563033691	chr7:6681427-6681428	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs567514925	chr7:6681507-6681508	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs376022636	chr7:6681525-6681526	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs73348733	chr7:6681547-6681548	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546727858	chr7:6681576-6681577	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs201073259	chr7:6681587-6681588	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs940870	chr7:6681619-6681620	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538649556	chr7:6681658-6681659	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs115798817	chr7:6681660-6681661	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs569516950	chr7:6681679-6681680	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs371142400	chr7:6681682-6681683	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs186157925	chr7:6681740-6681741	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs139138466	chr7:6681742-6681743	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs573139506	chr7:6681744-6681745	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs540285762	chr7:6681746-6681747	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs190009677	chr7:6681791-6681792	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs542486363	chr7:6681811-6681812	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs544580851	chr7:6681820-6681821	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs562771917	chr7:6681865-6681866	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs200980933	chr7:6681927-6681928	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs560656325	chr7:6681932-6681933	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs542595800	chr7:6681937-6681938	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs541340917	chr7:6681938-6681939	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs561024468	chr7:6681942-6681943	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs528297003	chr7:6681987-6681988	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs546689434	chr7:6681989-6681990	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs571379366	chr7:6681995-6681996	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs79944099	chr7:6682037-6682038	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs376552997	chr7:6682046-6682047	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568804170	chr7:6682057-6682058	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs536939901	chr7:6682064-6682065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6678000-6691600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:6678200-6681200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:6678200-6681600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:6678200-6681600	Weak transcription	Fetal Kidney	kidney
5	chr7:6678200-6682400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:6678200-6683200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr7:6678200-6683400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr7:6678200-6683800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr7:6678200-6684200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr7:6678200-6685000	Strong transcription	NHEK	skin
11	chr7:6678200-6698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr7:6678400-6681200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr7:6678400-6683000	Weak transcription	Small Intestine	intestine
14	chr7:6678400-6691600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:6678400-6691600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:6678600-6681200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:6678600-6681200	Weak transcription	Brain Angular Gyrus	brain
18	chr7:6678600-6681600	Weak transcription	HUVEC	blood vessel
19	chr7:6678600-6682800	Weak transcription	Stomach Mucosa	stomach
20	chr7:6678600-6687800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:6678600-6687800	Strong transcription	Fetal Intestine Large	intestine
22	chr7:6678600-6689600	Strong transcription	Fetal Intestine Small	intestine
23	chr7:6678800-6681400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:6678800-6681400	Strong transcription	HSMM	muscle
25	chr7:6678800-6681600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr7:6678800-6682000	Weak transcription	Psoas Muscle	Psoas
27	chr7:6678800-6685600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:6678800-6688600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:6678800-6689600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:6678800-6691200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:6678800-6691400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:6679000-6681200	Weak transcription	Fetal Lung	lung
33	chr7:6679000-6681400	Strong transcription	Primary B cells from cord blood	blood
34	chr7:6679000-6681800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr7:6679000-6682800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr7:6679000-6684600	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr7:6679000-6684800	Strong transcription	A549	lung
38	chr7:6679000-6687800	Strong transcription	Fetal Stomach	stomach
39	chr7:6679000-6689200	Strong transcription	Thymus	Thymus
40	chr7:6679000-6689400	Strong transcription	Fetal Thymus	thymus
41	chr7:6679000-6689600	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr7:6679000-6690000	Strong transcription	Fetal Brain Female	brain
43	chr7:6679000-6692200	Strong transcription	Primary T cells from cord blood	blood
44	chr7:6679000-6692600	Strong transcription	Primary B cells from peripheral blood	blood
45	chr7:6679000-6695200	Strong transcription	Stomach Smooth Muscle	stomach
46	chr7:6679000-6695400	Strong transcription	Brain Inferior Temporal Lobe	brain
47	chr7:6679200-6681400	Strong transcription	HMEC	breast
48	chr7:6679200-6681600	Genic enhancers	Spleen	Spleen
49	chr7:6679200-6690200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr7:6679200-6690200	Strong transcription	Lung	lung

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