Variant report

Variant	rs1168976
Chromosome Location	chr2:96813480-96813481
allele	C/T
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	GATA3	chr2:96811975-96813622	SK-N-SH	brain:	n/a	chr2:96812929-96812938 chr2:96812928-96812938 chr2:96812928-96812936 chr2:96812929-96812936
2	CTCF	chr2:96813380-96813530	HepG2	liver:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
3	CTCF	chr2:96813361-96813542	GM12891	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
4	WRNIP1	chr2:96813130-96813725	GM12878	blood:	n/a	n/a
5	USF2	chr2:96812627-96813562	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr2:96813380-96813530	GM12865	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
7	RUNX3	chr2:96813194-96813873	GM12878	blood:	n/a	n/a
8	ESRRA	chr2:96807401-96815327	GM12878	blood:	n/a	chr2:96814549-96814568 chr2:96812831-96812844 chr2:96814530-96814543 chr2:96808836-96808848 chr2:96812889-96812902
9	SMARCC1	chr2:96813402-96815037	Hela-S3	cervix:	n/a	chr2:96814390-96814399
10	CTCF	chr2:96813420-96813570	HEK293	kidney:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
11	POLR2A	chr2:96813306-96813894	GM12878	blood:	n/a	n/a
12	CTCF	chr2:96813420-96813570	WERI-Rb-1	eye:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
13	CHD1	chr2:96813304-96813499	GM12878	blood:	n/a	n/a
14	MAZ	chr2:96813396-96814820	IMR90	lung:	n/a	chr2:96814534-96814544
15	CTCF	chr2:96813400-96813550	GM12872	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
16	MAZ	chr2:96813353-96813615	GM12878	blood:	n/a	n/a
17	CTCF	chr2:96813369-96813510	HepG2	liver:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
18	POLR2A	chr2:96813354-96814609	GM12878	blood:	n/a	n/a
19	MYC	chr2:96809973-96813599	Hela-S3	cervix:	n/a	chr2:96811287-96811296 chr2:96812004-96812014
20	CTCF	chr2:96813340-96813490	Hela-S3	cervix:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
21	EP300	chr2:96811760-96815004	SK-N-SH	brain:	n/a	chr2:96813968-96813982 chr2:96812145-96812161 chr2:96812146-96812162
22	CTCF	chr2:96813340-96813490	GM12864	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
23	PML	chr2:96806496-96814786	GM12878	blood:	n/a	chr2:96814389-96814398
24	CTCF	chr2:96813440-96813590	GM12875	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
25	POLR2A	chr2:96802923-96814679	GM12891	blood:	n/a	n/a
26	TFAP2C	chr2:96811756-96813708	Hela-S3	cervix:	n/a	n/a
27	EP300	chr2:96813277-96815068	GM12878	blood:	n/a	chr2:96813968-96813982
28	CTCF	chr2:96813418-96813535	GM12878	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
29	CTCF	chr2:96813340-96813490	HPAF	blood vessel:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
30	CTCF	chr2:96813365-96813552	GM19239	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
31	CHD2	chr2:96813401-96814920	GM12878	blood:	n/a	chr2:96814302-96814312
32	CTCF	chr2:96813340-96813490	GM12869	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
33	POLR2A	chr2:96797189-96814534	GM12892	blood:	n/a	n/a
34	RUNX3	chr2:96813267-96813615	GM12878	blood:	n/a	n/a
35	CTCF	chr2:96813340-96813490	GM12868	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
36	MTA3	chr2:96806625-96815107	GM12878	blood:	n/a	n/a
37	CTCF	chr2:96813400-96813550	GM12874	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
38	TBP	chr2:96813201-96813553	GM12878	blood:	n/a	n/a
39	POLR2A	chr2:96806534-96814566	GM12891	blood:	n/a	n/a
40	POLR2A	chr2:96802751-96813556	GM12892	blood:	n/a	n/a
41	KAP1	chr2:96812525-96814932	HEK293	kidney:	n/a	chr2:96814389-96814398
42	BHLHE40	chr2:96813184-96814837	GM12878	blood:	n/a	n/a
43	POLR2A	chr2:96806172-96813481	GM12892	blood:	n/a	n/a
44	MAX	chr2:96812704-96813588	Hela-S3	cervix:	n/a	n/a
45	TCF12	chr2:96812603-96813483	MCF-7	breast:	n/a	chr2:96812968-96812976
46	POLR2A	chr2:96813013-96813980	GM12878	blood:	n/a	n/a
47	ZNF143	chr2:96813362-96813682	GM12878	blood:	n/a	n/a
48	CTCF	chr2:96813397-96813520	GM13976	blood:	n/a	chr2:96813447-96813468 chr2:96813452-96813470
49	POLR2A	chr2:96803003-96814644	GM12878	blood:	n/a	n/a
50	MAX	chr2:96813216-96813885	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96813186..96815760-chr2:96873244..96875582,3	MCF-7	breast:
2	chr2:96781942..96784647-chr2:96809826..96814461,4	MCF-7	breast:
3	chr2:96812496..96814407-chr2:96931175..96932948,2	MCF-7	breast:
4	chr2:96808076..96814305-chr2:96871431..96875215,8	MCF-7	breast:
5	chr2:96812916..96814521-chr2:96834826..96836596,2	K562	blood:

Variant related genes	Relation type
ENSG00000228873	TF binding region
DUSP2	TF binding region
ENSG00000135956	Chromatin interaction
ENSG00000222040	Chromatin interaction
ENSG00000144021	Chromatin interaction
ENSG00000084090	Chromatin interaction
ENSG00000204685	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10183151	0.95[CEU][hapmap];0.80[YRI][hapmap];0.91[EUR][1000 genomes]
rs1030864	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11680950	1.00[ASW][hapmap];0.95[CEU][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs11687113	0.92[GIH][hapmap]
rs1168965	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.81[MEX][hapmap];0.91[TSI][hapmap];0.80[YRI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1168966	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs1168967	0.83[EUR][1000 genomes]
rs1168968	1.00[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1168970	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1168972	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1168974	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1168975	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11693248	0.83[EUR][1000 genomes]
rs13019188	0.80[CEU][hapmap]
rs1657502	0.82[CEU][hapmap];0.84[GIH][hapmap];0.80[EUR][1000 genomes]
rs1724121	0.85[EUR][1000 genomes]
rs1724125	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2140938	0.84[EUR][1000 genomes]
rs2229169	0.95[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2301707	1.00[CEU][hapmap];0.81[MEX][hapmap];0.82[TSI][hapmap]
rs2312955	0.90[CEU][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.91[TSI][hapmap];0.80[YRI][hapmap];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2438978	0.80[YRI][hapmap]
rs2462774	0.87[YRI][hapmap]
rs2576437	0.84[EUR][1000 genomes]
rs2579519	0.81[GIH][hapmap]
rs2579549	0.85[EUR][1000 genomes]
rs2579550	0.86[EUR][1000 genomes]
rs2579552	0.87[EUR][1000 genomes]
rs2692893	0.84[ASW][hapmap];0.86[CEU][hapmap];0.82[CHB][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.88[TSI][hapmap];0.89[EUR][1000 genomes]
rs2692894	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.85[MEX][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2692934	0.86[EUR][1000 genomes]
rs2692936	0.86[EUR][1000 genomes]
rs2692937	0.87[EUR][1000 genomes]
rs2917662	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2969490	0.86[CEU][hapmap];0.86[GIH][hapmap];0.84[EUR][1000 genomes]
rs2969491	0.95[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3111873	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3821051	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.90[JPT][hapmap];0.85[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes]
rs4144055	0.91[GIH][hapmap];0.88[YRI][hapmap]
rs4426564	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.91[TSI][hapmap];0.80[YRI][hapmap]
rs4907288	0.89[YRI][hapmap]
rs4907299	0.90[CEU][hapmap];0.85[GIH][hapmap];0.90[EUR][1000 genomes]
rs58448550	0.83[EUR][1000 genomes]
rs6740563	0.89[YRI][hapmap]
rs749457	0.82[CEU][hapmap];0.84[GIH][hapmap];0.83[EUR][1000 genomes]
rs749459	0.82[CEU][hapmap];0.84[GIH][hapmap]
rs7561198	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7604842	0.95[CEU][hapmap];0.91[EUR][1000 genomes]
rs772175	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.98[CHD][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap];0.97[TSI][hapmap];0.88[YRI][hapmap]
rs772178	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.98[CHD][hapmap];0.95[JPT][hapmap];0.86[MEX][hapmap];0.85[MKK][hapmap];0.97[TSI][hapmap];0.88[YRI][hapmap]
rs893173	0.82[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1840487	chr2:96582807-96836512	Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv874673	chr2:96647856-96825363	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	esv1825266	chr2:96704118-96830753	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1004129	chr2:96738585-96825363	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv933671	chr2:96739308-97652262	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
6	nsv1000780	chr2:96740430-97671395	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
7	nsv535826	chr2:96740430-97671395	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
8	nsv874675	chr2:96741944-96825363	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
9	nsv874676	chr2:96753149-96825363	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
10	esv1819594	chr2:96755038-96833480	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	nsv1008495	chr2:96755070-96825363	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
12	nsv1002392	chr2:96756289-96815149	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
13	nsv874677	chr2:96756547-97717345	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
14	nsv1004977	chr2:96757107-96819188	Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
15	nsv1015000	chr2:96757107-96825363	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
16	nsv1001204	chr2:96766559-97728507	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
17	nsv535827	chr2:96766559-97728507	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS 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 miRNA target site	162 gene(s)	inside rSNPs	diseases
18	nsv1007132	chr2:96767204-96829489	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs1168976	FAHD2CP	cis	lung	GTEx
rs1168976	MGAT4A	cis	parietal	SCAN
rs1168976	MRPL30	cis	parietal	SCAN
rs1168976	GPAT2	cis	Muscle Skeletal	GTEx
rs1168976	AC008268.2	cis	Adipose Subcutaneous	GTEx
rs1168976	FAHD2CP	cis	Muscle Skeletal	GTEx
rs1168976	CIAO1	cis	Skin Sun Exposed Lower leg	GTEx
rs1168976	GPAT2	cis	Adipose Subcutaneous	GTEx
rs1168976	SNRNP200	cis	cerebellum	SCAN
rs1168976	ADRA2B	cis	Nerve Tibial	GTEx
rs1168976	ADRA2B	cis	Thyroid	GTEx

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96810000-96815000	Enhancers	Fetal Heart	heart
2	chr2:96810400-96815000	Enhancers	Fetal Lung	lung
3	chr2:96811200-96814000	Weak transcription	HUVEC	blood vessel
4	chr2:96811200-96814400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr2:96811200-96814400	Weak transcription	Gastric	stomach
6	chr2:96811200-96814600	Enhancers	Spleen	Spleen
7	chr2:96811200-96814800	Enhancers	Lung	lung
8	chr2:96811200-96815000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:96811200-96815000	Enhancers	NH-A	brain
10	chr2:96811200-96815200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:96811400-96814200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr2:96811400-96814200	Weak transcription	A549	lung
13	chr2:96811400-96814400	Enhancers	Right Atrium	heart
14	chr2:96811400-96814600	Enhancers	Osteobl	bone
15	chr2:96811400-96814800	Flanking Active TSS	Fetal Thymus	thymus
16	chr2:96811400-96815000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
17	chr2:96811400-96815200	Flanking Active TSS	Hela-S3	cervix
18	chr2:96811600-96813800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr2:96811600-96813800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr2:96811600-96813800	Enhancers	Brain Anterior Caudate	brain
21	chr2:96811600-96814000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:96811600-96814200	Weak transcription	Pancreas	Pancrea
23	chr2:96811600-96814400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr2:96811600-96814600	Enhancers	Left Ventricle	heart
25	chr2:96811600-96814600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr2:96811600-96815000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:96811600-96815000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr2:96811600-96815000	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr2:96811600-96815000	Enhancers	Right Ventricle	heart
30	chr2:96811600-96815000	Enhancers	HMEC	breast
31	chr2:96811600-96815200	Enhancers	Fetal Stomach	stomach
32	chr2:96811800-96814200	Enhancers	Colonic Mucosa	Colon
33	chr2:96811800-96814400	Enhancers	K562	blood
34	chr2:96811800-96814800	Enhancers	Adipose Nuclei	Adipose
35	chr2:96811800-96815000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr2:96811800-96815200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:96812000-96813600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr2:96812200-96813800	Enhancers	Fetal Intestine Small	intestine
39	chr2:96812200-96814000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr2:96812200-96815000	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr2:96812200-96815200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr2:96812400-96813800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:96812400-96814000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr2:96812400-96814200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr2:96812400-96814200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
46	chr2:96812400-96814400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr2:96812400-96815000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr2:96812400-96815000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr2:96812400-96815000	Flanking Active TSS	Thymus	Thymus
50	chr2:96812400-96815200	Enhancers	Primary monocytes fromperipheralblood	blood

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