Variant report

Variant	rs1293297
Chromosome Location	chr8:11711473-11711474
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EGR1	chr8:11711302-11711693	K562	blood:	n/a	n/a
2	FOSL2	chr8:11711164-11712058	A549	lung:	n/a	chr8:11711662-11711674 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711627-11711638 chr8:11711664-11711672
3	JUND	chr8:11711258-11711948	MCF-7	breast:	n/a	chr8:11711662-11711674 chr8:11711662-11711673 chr8:11711663-11711673 chr8:11711628-11711639 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711664-11711672
4	ZBTB7A	chr8:11711368-11711873	K562	blood:	n/a	n/a
5	MBD4	chr8:11710454-11711868	HepG2	liver:	n/a	n/a
6	FOSL2	chr8:11711342-11711909	MCF-7	breast:	n/a	chr8:11711662-11711674 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711627-11711638 chr8:11711664-11711672
7	RAD21	chr8:11711294-11711867	SK-N-SH_RA	brain:	n/a	chr8:11711376-11711386
8	MAZ	chr8:11711308-11711808	K562	blood:	n/a	chr8:11711629-11711638
9	POLR2A	chr8:11709880-11711785	HepG2	liver:	n/a	n/a
10	ELF1	chr8:11711325-11711688	K562	blood:	n/a	chr8:11711548-11711561 chr8:11711550-11711559
11	GATA3	chr8:11711334-11711903	MCF-7	breast:	n/a	n/a
12	EP300	chr8:11711391-11711695	K562	blood:	n/a	n/a
13	ELF1	chr8:11711275-11711852	MCF-7	breast:	n/a	chr8:11711548-11711561 chr8:11711550-11711559
14	BHLHE40	chr8:11711404-11711808	HepG2	liver:	n/a	chr8:11711744-11711760
15	JUND	chr8:11711186-11712131	HCT-116	colon:	n/a	chr8:11711662-11711674 chr8:11711662-11711673 chr8:11711663-11711673 chr8:11711628-11711639 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711664-11711672
16	EP300	chr8:11711273-11711914	A549	lung:	n/a	n/a
17	POLR2A	chr8:11710837-11711945	IMR90	lung:	n/a	n/a
18	EP300	chr8:11711341-11711839	HepG2	liver:	n/a	n/a
19	JUN	chr8:11711442-11711858	Hela-S3	cervix:	n/a	chr8:11711662-11711674 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711664-11711672
20	ELF1	chr8:11711265-11711777	MCF-7	breast:	n/a	chr8:11711548-11711561 chr8:11711550-11711559
21	NR2F2	chr8:11711210-11711959	MCF-7	breast:	n/a	n/a
22	MYC	chr8:11711448-11711797	K562	blood:	n/a	chr8:11711629-11711638
23	FOSL2	chr8:11711384-11711934	MCF-7	breast:	n/a	chr8:11711662-11711674 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711627-11711638 chr8:11711664-11711672
24	POLR2A	chr8:11709890-11711820	ECC-1	luminal epithelium:	n/a	n/a
25	JUN	chr8:11711192-11712054	K562	blood:	n/a	chr8:11711662-11711674 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711664-11711672
26	JUND	chr8:11711342-11711857	HepG2	liver:	n/a	chr8:11711662-11711674 chr8:11711662-11711673 chr8:11711663-11711673 chr8:11711628-11711639 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711664-11711672
27	RAD21	chr8:11711332-11711763	HepG2	liver:	n/a	chr8:11711376-11711386
28	HA-E2F1	chr8:11711464-11711907	MCF-7	breast:	n/a	n/a
29	ZMIZ1	chr8:11711455-11711871	K562	blood:	n/a	n/a
30	EP300	chr8:11711280-11711920	SK-N-SH_RA	brain:	n/a	n/a
31	MAX	chr8:11711440-11711889	SK-N-SH	brain:	n/a	chr8:11711629-11711638
32	POLR2A	chr8:11711270-11711898	HepG2	liver:	n/a	n/a
33	EP300	chr8:11711275-11711838	SK-N-SH_RA	brain:	n/a	n/a
34	MAZ	chr8:11711306-11711939	HepG2	liver:	n/a	chr8:11711629-11711638
35	MYBL2	chr8:11710206-11711935	HepG2	liver:	n/a	n/a
36	MXI1	chr8:11710999-11712083	IMR90	lung:	n/a	n/a
37	HDAC2	chr8:11711390-11711745	K562	blood:	n/a	n/a
38	MXI1	chr8:11710307-11711889	HepG2	liver:	n/a	n/a
39	TCF12	chr8:11711179-11711976	ECC-1	luminal epithelium:	n/a	n/a
40	EGR1	chr8:11711169-11711783	MCF-7	breast:	n/a	n/a
41	POLR2A	chr8:11709082-11711980	HepG2	liver:	n/a	n/a
42	POLR2A	chr8:11709121-11711899	K562	blood:	n/a	n/a
43	EGR1	chr8:11711268-11711750	ECC-1	luminal epithelium:	n/a	n/a
44	TAF1	chr8:11711416-11711795	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr8:11710114-11711913	HUVEC	blood vessel:	n/a	n/a
46	TAF1	chr8:11711274-11711821	K562	blood:	n/a	n/a
47	SIN3AK20	chr8:11711267-11711817	SK-N-SH	brain:	n/a	n/a
48	FOSL2	chr8:11711259-11711993	SK-N-SH	brain:	n/a	chr8:11711662-11711674 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711627-11711638 chr8:11711664-11711672
49	FOSL1	chr8:11711415-11711830	K562	blood:	n/a	chr8:11711628-11711639 chr8:11711662-11711674 chr8:11711663-11711673 chr8:11711662-11711673 chr8:11711663-11711673 chr8:11711663-11711673 chr8:11711630-11711639 chr8:11711660-11711671 chr8:11711663-11711673 chr8:11711664-11711672
50	TCF12	chr8:11711149-11712038	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:11710197..11714536-chr8:11724997..11727273,4	K562	blood:
2	chr8:11706164..11707709-chr8:11709253..11711783,2	K562	blood:
3	chr8:11708512..11715317-chr8:11723234..11727095,9	MCF-7	breast:
4	chr8:11710836..11712408-chr8:11724380..11726355,2	MCF-7	breast:
5	chr8:11709901..11713097-chr8:11718255..11721625,5	MCF-7	breast:
6	chr8:11665243..11667469-chr8:11710761..11712863,3	MCF-7	breast:
7	chr8:11708825..11713035-chr8:11718721..11724039,7	MCF-7	breast:
8	chr8:11701923..11705144-chr8:11709953..11712815,3	K562	blood:

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000079459	Chromatin interaction
ENSG00000269899	Chromatin interaction
ENSG00000164733	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1122182	1.00[CHB][hapmap]
rs1293292	1.00[CHB][hapmap]
rs1293294	1.00[CHB][hapmap]
rs1293298	1.00[CHB][hapmap]
rs1293300	1.00[CHB][hapmap]
rs1692811	1.00[CHB][hapmap]
rs1692821	1.00[CHB][hapmap]
rs1736081	1.00[CHB][hapmap]
rs1736086	1.00[CHB][hapmap]
rs2740592	1.00[CHB][hapmap]
rs3947	1.00[CHB][hapmap]
rs4839	1.00[CHB][hapmap]
rs4840581	1.00[CHB][hapmap]
rs6988241	1.00[CHB][hapmap]
rs709821	1.00[CHB][hapmap]
rs709822	1.00[CHB][hapmap]
rs7461560	1.00[CHB][hapmap]
rs7831946	1.00[CHB][hapmap]
rs7836601	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv1023803	chr8:11623570-11721655	Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv539476	chr8:11623570-11721655	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv890361	chr8:11625808-11755513	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	nsv890362	chr8:11625808-11771089	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1032739	chr8:11643803-11716473	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
15	nsv890365	chr8:11666451-11735641	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv1031158	chr8:11666558-11759064	Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv539477	chr8:11666558-11759064	Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv890367	chr8:11668153-11793529	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
21	nsv890368	chr8:11671041-11718528	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
22	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
23	nsv1016952	chr8:11679271-11849955	Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
24	nsv1029093	chr8:11679271-11858466	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
25	nsv539478	chr8:11679271-11858466	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv1017334	chr8:11688534-11732949	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
27	nsv539479	chr8:11688534-11732949	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
28	nsv1019738	chr8:11696393-11732949	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
29	nsv539480	chr8:11696393-11732949	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
30	nsv1031972	chr8:11696393-11805961	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
31	nsv539481	chr8:11696393-11805961	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
32	esv34042	chr8:11698337-11726817	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
33	nsv610293	chr8:11698747-11929734	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
34	nsv516685	chr8:11698747-12570199	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
35	nsv972525	chr8:11706325-11714357	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11675800-11712600	Strong transcription	Dnd41	blood
2	chr8:11677600-11711800	Strong transcription	Fetal Brain Female	brain
3	chr8:11679000-11715200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr8:11682200-11713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr8:11682400-11712600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:11683000-11713200	Strong transcription	Primary B cells from peripheral blood	blood
7	chr8:11683400-11711600	Strong transcription	Brain Germinal Matrix	brain
8	chr8:11683600-11712600	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr8:11698600-11716600	Strong transcription	Primary T cells from cord blood	blood
10	chr8:11700600-11721200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:11703000-11721200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr8:11703400-11718800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:11704400-11715600	Weak transcription	GM12878-XiMat	blood
14	chr8:11705200-11722400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:11705200-11723000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr8:11706600-11724400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr8:11706800-11723000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr8:11706800-11724400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr8:11707600-11713400	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr8:11708400-11713200	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr8:11708600-11716200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr8:11708600-11718200	Weak transcription	Aorta	Aorta
23	chr8:11708600-11724600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:11709400-11718200	Weak transcription	Fetal Kidney	kidney
25	chr8:11709800-11712000	Genic enhancers	Placenta	Placenta
26	chr8:11710000-11711800	Enhancers	Right Atrium	heart
27	chr8:11710000-11712000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr8:11710000-11712000	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr8:11710000-11712200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:11710000-11712200	Genic enhancers	Lung	lung
31	chr8:11710000-11713000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr8:11710000-11714000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr8:11710200-11712000	Enhancers	Ovary	ovary
34	chr8:11710200-11712400	Genic enhancers	Sigmoid Colon	Sigmoid Colon
35	chr8:11710200-11712600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:11710200-11712800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr8:11710200-11713000	Genic enhancers	Fetal Intestine Large	intestine
38	chr8:11710200-11713200	Genic enhancers	Fetal Intestine Small	intestine
39	chr8:11710400-11711800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:11710400-11711800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:11710400-11712000	Enhancers	Brain Anterior Caudate	brain
42	chr8:11710400-11712600	Enhancers	Fetal Heart	heart
43	chr8:11710400-11712600	Strong transcription	Thymus	Thymus
44	chr8:11710400-11712600	Genic enhancers	NHDF-Ad	bronchial
45	chr8:11710600-11711600	Genic enhancers	Brain Hippocampus Middle	brain
46	chr8:11710600-11711800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr8:11710600-11711800	Flanking Active TSS	Colonic Mucosa	Colon
48	chr8:11710600-11711800	Genic enhancers	Fetal Muscle Trunk	muscle
49	chr8:11710600-11712000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr8:11710600-11712000	Enhancers	HUES6 Cell Line	embryonic stem cell

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