Variant report

Variant	rs5759668
Chromosome Location	chr22:23606384-23606385
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:17)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:17 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr22:23605374-23608089	K562	blood:	n/a	n/a
2	POLR2A	chr22:23605743-23607124	K562	blood:	n/a	n/a
3	POLR2A	chr22:23606199-23606761	HL-60	blood:	n/a	n/a
4	POLR2A	chr22:23606113-23606701	GM12878	blood:	n/a	n/a
5	POLR2A	chr22:23606174-23606678	HL-60	blood:	n/a	n/a
6	POLR2A	chr22:23606072-23606838	GM12878	blood:	n/a	n/a
7	POLR2A	chr22:23604082-23607119	K562	blood:	n/a	n/a
8	POLR2A	chr22:23601916-23608354	K562	blood:	n/a	n/a
9	THAP1	chr22:23606269-23607103	K562	blood:	n/a	n/a
10	RUNX3	chr22:23606036-23606495	GM12878	blood:	n/a	n/a
11	POLR2A	chr22:23606151-23606409	H1-hESC	embryonic stem cell:	n/a	n/a
12	ETS1	chr22:23605969-23606769	K562	blood:	n/a	n/a
13	POLR2A	chr22:23606004-23606668	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr22:23603966-23607216	K562	blood:	n/a	n/a
15	GATA2	chr22:23605871-23607007	K562	blood:	n/a	n/a
16	ELF1	chr22:23606162-23607116	GM12878	blood:	n/a	chr22:23606927-23606940
17	EBF1	chr22:23606182-23606503	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:23606384-23606434	HAEpiC	amniotic membrane:	n/a
2	chr22:23606384-23606434	NHBE	bronchial:	n/a
3	chr22:23606384-23606434	HPAEpiC	pulmonary alveolar:	n/a
4	chr22:23606384-23606434	GM12878	blood:	n/a
5	chr22:23606384-23606434	A549	lung:	n/a
6	chr22:23606384-23606434	SK-N-MC	brain:	n/a
7	chr22:23606384-23606434	IMR90	lung:	fetal
8	chr22:23606384-23606434	Jurkat	blood:	n/a
9	chr22:23606384-23606434	K562	blood:	n/a
10	chr22:23606384-23606434	GM19239	blood:	n/a
11	chr22:23606384-23606434	AG04450	lung:	fetal
12	chr22:23606384-23606434	U87	brain:	n/a
13	chr22:23606384-23606434	HepG2	liver:	n/a
14	chr22:23606384-23606434	HCF	heart:	n/a
15	chr22:23606384-23606434	HCT-116	colon:	n/a
16	chr22:23606384-23606434	AG09309	skin:	n/a
17	chr22:23606384-23606434	SAEC	small airway:	n/a
18	chr22:23606384-23606434	GM06990	blood:	n/a
19	chr22:23606384-23606434	SK-N-SH_RA	brain:	n/a
20	chr22:23606384-23606434	HRE	kidney:	n/a
21	chr22:23606384-23606434	HRCEpiC	kidney:	n/a
22	chr22:23606384-23606434	SKMC	muscle:	n/a
23	chr22:23606384-23606434	GM12892	blood:	n/a
24	chr22:23606384-23606434	AG09319	gingival:	n/a
25	chr22:23606384-23606434	HCM	heart:	n/a
26	chr22:23606384-23606434	MCF10A-Er-Src	breast:	n/a
27	chr22:23606384-23606434	BE2_C	brain:	n/a
28	chr22:23606384-23606434	HNPCEpiC	eye:	n/a
29	chr22:23606384-23606434	BJ	skin:	n/a
30	chr22:23606384-23606434	HRPEpiC	eye:	n/a
31	chr22:23606384-23606434	HIPEpiC	eye:	n/a
32	chr22:23606384-23606434	AG04449	skin:	fetal
33	chr22:23606384-23606434	AoSMC	blood vessel:	n/a
34	chr22:23606384-23606434	RPTEC	kidney:	n/a
35	chr22:23606384-23606434	PANC-1	pancreas:	n/a
36	chr22:23606384-23606434	CMK	blood:	n/a
37	chr22:23606384-23606434	NHDF-neo	bronchial:	n/a
38	chr22:23606384-23606434	LNCaP	prostate:	n/a
39	chr22:23606384-23606434	HL-60	blood:	n/a
40	chr22:23606384-23606434	HMEC	breast:	n/a
41	chr22:23606384-23606434	GM12891	blood:	n/a
42	chr22:23606384-23606434	ECC-1	luminal epithelium:	n/a
43	chr22:23606384-23606434	AG10803	skin:	n/a
44	chr22:23606384-23606434	SK-N-SH	brain:	n/a
45	chr22:23606384-23606434	MCF-7	breast:	n/a
46	chr22:23606384-23606434	Hela-S3	cervix:	n/a
47	chr22:23606384-23606434	HCPEpiC	choroid plexus:	n/a
48	chr22:23606384-23606434	HEK293	kidney:	embryo
49	chr22:23606384-23606434	H1-hESC	embryonic stem cell:	embryo
50	chr22:23606384-23606434	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:23521575..23523250-chr22:23605169..23607302,2	MCF-7	breast:
2	chr22:23520987..23523573-chr22:23606117..23609416,6	MCF-7	breast:
3	chr22:23605943..23609700-chr22:23610054..23612311,4	MCF-7	breast:

No data

Variant related genes	Relation type
RN7SL263P	TF binding region
RN7SL263P	CpG island
ENSG00000186716	Chromatin interaction
ENSG00000236794	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11090227	0.96[ASN][1000 genomes]
rs11090228	0.85[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs12166802	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs12233352	1.00[CEU][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs16802	0.83[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1811017	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1811018	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2227939	0.91[ASN][1000 genomes]
rs2267022	1.00[JPT][hapmap]
rs2330369	0.90[YRI][hapmap];0.87[AFR][1000 genomes]
rs3788358	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.80[YRI][hapmap];0.96[ASN][1000 genomes]
rs3788360	1.00[JPT][hapmap]
rs4822379	0.85[CHB][hapmap]
rs5751619	0.91[ASN][1000 genomes]
rs5751620	0.82[CHB][hapmap];0.83[ASN][1000 genomes]
rs5759661	0.81[ASN][1000 genomes]
rs5759665	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs5759666	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs5759669	0.86[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs5759670	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs5759671	0.85[CHB][hapmap];0.85[TSI][hapmap];0.83[ASN][1000 genomes]
rs5759673	0.96[ASN][1000 genomes]
rs5759675	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs5759676	1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs5759679	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs5759680	0.83[ASN][1000 genomes]
rs5759681	0.85[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs5759682	0.85[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs5996508	0.96[ASN][1000 genomes]
rs5996509	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6003593	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6003598	0.96[ASN][1000 genomes]
rs6003600	0.96[ASN][1000 genomes]
rs62219796	0.89[ASN][1000 genomes]
rs7292656	0.91[ASN][1000 genomes]
rs9608093	0.87[ASN][1000 genomes]
rs9608100	0.91[ASN][1000 genomes]
rs9608102	0.85[CHB][hapmap]
rs9612269	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9624072	0.83[ASN][1000 genomes]
rs9624073	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915235	chr22:22971768-23650987	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
2	esv3388845	chr22:22973346-23652447	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	100 gene(s)	inside rSNPs	diseases
3	nsv531799	chr22:22993679-23642142	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
4	nsv1061433	chr22:22997799-23649107	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
5	nsv521695	chr22:22998337-23648009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
6	nsv915236	chr22:22998337-23650987	Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
7	nsv588512	chr22:22998337-23667731	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv531800	chr22:23002708-23648163	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
9	nsv916593	chr22:23002709-23648790	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
10	nsv993496	chr22:23002709-23654222	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh 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 miRNA	97 gene(s)	inside rSNPs	diseases
11	nsv1067002	chr22:23007167-23643363	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
12	nsv1067324	chr22:23007367-23654223	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
13	nsv533839	chr22:23012013-23643223	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
14	nsv916933	chr22:23012069-23654237	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
15	nsv531801	chr22:23028586-23657804	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	92 gene(s)	inside rSNPs	diseases
16	nsv531802	chr22:23046186-23627391	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	85 gene(s)	inside rSNPs	diseases
17	nsv1060509	chr22:23055148-23648719	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
18	nsv1056324	chr22:23055148-23750989	Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
19	nsv1062780	chr22:23060449-23648719	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
20	nsv948942	chr22:23063178-23645718	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv1063200	chr22:23097177-23643224	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	80 gene(s)	inside rSNPs	diseases
22	nsv949250	chr22:23157485-23645718	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
23	nsv1057659	chr22:23400739-24138788	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
24	nsv588598	chr22:23530168-23638025	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
25	nsv9876	chr22:23563331-23923059	Strong transcription Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
26	nsv482557	chr22:23584948-23741799	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
27	nsv531550	chr22:23589667-24012550	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
28	esv2762117	chr22:23592136-23996869	Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
29	nsv1063476	chr22:23596683-23989388	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
30	nsv544617	chr22:23596683-23989388	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
31	nsv1059951	chr22:23597270-23973060	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
32	nsv1060339	chr22:23603429-23984195	Bivalent/Poised TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
33	nsv544618	chr22:23603429-23984195	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23591000-23615800	Weak transcription	NH-A	brain
2	chr22:23593000-23618000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr22:23594400-23611800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr22:23594400-23614200	Weak transcription	A549	lung
5	chr22:23595000-23610800	Strong transcription	K562	blood
6	chr22:23595000-23612200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr22:23595000-23612200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr22:23595000-23647000	Strong transcription	Dnd41	blood
9	chr22:23595200-23623600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr22:23595400-23623800	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr22:23595600-23607200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr22:23595600-23609200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr22:23595600-23619200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr22:23595600-23623600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr22:23595800-23608200	Strong transcription	Thymus	Thymus
16	chr22:23595800-23609000	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr22:23595800-23611600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr22:23595800-23621000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr22:23595800-23623400	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr22:23595800-23649600	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr22:23596000-23608200	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr22:23597800-23606600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr22:23597800-23611400	Weak transcription	Fetal Kidney	kidney
24	chr22:23598400-23608400	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr22:23599400-23607800	Strong transcription	HepG2	liver
26	chr22:23599400-23609400	Strong transcription	Fetal Thymus	thymus
27	chr22:23599400-23635000	Weak transcription	Small Intestine	intestine
28	chr22:23599600-23623000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr22:23599800-23608000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr22:23600000-23608000	Strong transcription	NHEK	skin
31	chr22:23600200-23632000	Strong transcription	Fetal Intestine Small	intestine
32	chr22:23600400-23607400	Strong transcription	Right Atrium	heart
33	chr22:23600400-23608200	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr22:23600600-23606600	Weak transcription	Stomach Mucosa	stomach
35	chr22:23600800-23619200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr22:23600800-23619800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr22:23601200-23623800	Weak transcription	Fetal Brain Male	brain
38	chr22:23601600-23610800	Weak transcription	Colon Smooth Muscle	Colon
39	chr22:23601800-23606600	Strong transcription	Brain Cingulate Gyrus	brain
40	chr22:23601800-23607200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr22:23601800-23641000	Strong transcription	Primary T cells from cord blood	blood
42	chr22:23602200-23607400	Strong transcription	Right Ventricle	heart
43	chr22:23602200-23608200	Strong transcription	Fetal Brain Female	brain
44	chr22:23602400-23608000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr22:23602400-23612400	Strong transcription	Stomach Smooth Muscle	stomach
46	chr22:23602400-23620600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr22:23602600-23610800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr22:23602800-23606400	Strong transcription	Pancreas	Pancrea
49	chr22:23602800-23607200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr22:23602800-23607600	Strong transcription	Colonic Mucosa	Colon

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