Variant report

Variant	rs10792421
Chromosome Location	chr11:63605177-63605178
allele	A/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	STAT5A	chr11:63604571-63605363	GM12878	blood:	n/a	chr11:63604681-63604693 chr11:63604675-63604687
2	PML	chr11:63604454-63605223	GM12878	blood:	n/a	n/a
3	RAD21	chr11:63604592-63605244	ECC-1	luminal epithelium:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
4	CTCF	chr11:63604327-63605388	A549	lung:	n/a	chr11:63604874-63604884 chr11:63604872-63604885 chr11:63604870-63604886 chr11:63604871-63604892 chr11:63604869-63604887 chr11:63604872-63604881
5	RAD21	chr11:63604448-63605539	SK-N-SH	brain:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
6	MAX	chr11:63604708-63605374	NB4	blood:	n/a	n/a
7	RAD21	chr11:63604536-63605251	MCF-7	breast:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
8	WRNIP1	chr11:63604669-63605203	GM12878	blood:	n/a	n/a
9	RAD21	chr11:63604466-63605367	A549	lung:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
10	CTCF	chr11:63604636-63605195	K562	blood:	n/a	chr11:63604874-63604884 chr11:63604872-63604885 chr11:63604870-63604886 chr11:63604871-63604892 chr11:63604869-63604887 chr11:63604872-63604881
11	SMC3	chr11:63604295-63605561	SK-N-SH	brain:	n/a	chr11:63604871-63604885 chr11:63605297-63605307 chr11:63604871-63604878
12	CTCF	chr11:63604367-63605417	HCT-116	colon:	n/a	chr11:63604874-63604884 chr11:63604872-63604885 chr11:63604870-63604886 chr11:63604871-63604892 chr11:63604869-63604887 chr11:63604872-63604881
13	CTCF	chr11:63605120-63605270	WI-38	lung:	n/a	n/a
14	CTCF	chr11:63604650-63605225	HCT-116	colon:	n/a	chr11:63604874-63604884 chr11:63604872-63604885 chr11:63604870-63604886 chr11:63604871-63604892 chr11:63604869-63604887 chr11:63604872-63604881
15	SMC3	chr11:63604574-63605297	GM12878	blood:	n/a	chr11:63604871-63604885 chr11:63604871-63604878
16	CTCF	chr11:63605060-63605210	AG04450	lung:	n/a	n/a
17	ZNF263	chr11:63604686-63605335	HEK293-T-REx	kidney:	n/a	chr11:63604940-63604961
18	RAD21	chr11:63604653-63605229	SK-N-SH_RA	brain:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
19	SMC3	chr11:63604577-63605419	Hela-S3	cervix:	n/a	chr11:63604871-63604885 chr11:63605297-63605307 chr11:63604871-63604878
20	RAD21	chr11:63604608-63605216	HepG2	liver:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
21	RAD21	chr11:63604616-63605189	H1-hESC	embryonic stem cell:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
22	RAD21	chr11:63604401-63605398	HCT-116	colon:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
23	RAD21	chr11:63604593-63605231	A549	lung:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
24	RAD21	chr11:63604498-63605277	MCF-7	breast:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
25	SPI1	chr11:63605116-63605741	HL-60	blood:	n/a	chr11:63605427-63605436 chr11:63605464-63605473 chr11:63605295-63605308 chr11:63605425-63605438
26	RAD21	chr11:63604581-63605182	ECC-1	luminal epithelium:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
27	CTCF	chr11:63605140-63605290	AG10803	skin:	n/a	n/a
28	POLR2A	chr11:63604511-63606793	GM12891	blood:	n/a	n/a
29	RAD21	chr11:63604478-63605555	HCT-116	colon:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
30	RAD21	chr11:63604645-63605230	IMR90	lung:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
31	RAD21	chr11:63604610-63605181	SK-N-SH_RA	brain:	n/a	chr11:63604871-63604885 chr11:63604870-63604889 chr11:63604874-63604883 chr11:63604873-63604886 chr11:63604875-63604885
32	MAZ	chr11:63604444-63605193	IMR90	lung:	n/a	n/a
33	NRF1	chr11:63605152-63605251	K562	blood:	n/a	n/a
34	CTCF	chr11:63604383-63605339	SK-N-SH	brain:	n/a	chr11:63604874-63604884 chr11:63604872-63604885 chr11:63604870-63604886 chr11:63604871-63604892 chr11:63604869-63604887 chr11:63604872-63604881
35	CHD2	chr11:63605172-63605325	GM12878	blood:	n/a	n/a
36	MTA3	chr11:63604593-63605308	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63604396..63605449-chr11:63668816..63670209,9	MCF-7	breast:
2	chr11:63534532..63537273-chr11:63602993..63606665,6	K562	blood:
3	chr11:63595369..63597909-chr11:63603609..63605330,2	MCF-7	breast:
4	chr11:63535378..63537033-chr11:63604393..63605415,6	MCF-7	breast:
5	chr11:63604982..63606649-chr11:63633551..63637040,3	K562	blood:
6	chr11:63603650..63606270-chr11:63705616..63707256,2	MCF-7	breast:
7	chr11:63535469..63537285-chr11:63604590..63607809,3	MCF-7	breast:
8	chr11:63535254..63537273-chr11:63604196..63606665,2	K562	blood:
9	chr11:63598165..63599939-chr11:63604514..63606107,2	MCF-7	breast:
10	chr11:63597538..63602989-chr11:63603448..63608044,6	K562	blood:
11	chr11:63604037..63605385-chr11:63668805..63669828,8	MCF-7	breast:
12	chr11:63604465..63605390-chr11:63673837..63675145,8	MCF-7	breast:
13	chr11:63605131..63609420-chr11:63682910..63687369,4	MCF-7	breast:
14	chr11:63604963..63609785-chr11:63634052..63642181,26	MCF-7	breast:
15	chr11:63535587..63536320-chr11:63604648..63605301,2	MCF-7	breast:
16	chr11:63603311..63612666-chr11:63664740..63679491,25	MCF-7	breast:
17	chr11:63604824..63606885-chr11:63683071..63686195,3	K562	blood:
18	chr11:63604931..63605437-chr11:63712924..63713689,2	MCF-7	breast:
19	chr11:63579552..63584409-chr11:63604789..63609677,6	K562	blood:
20	chr11:63604628..63605373-chr11:63655293..63655881,2	K562	blood:
21	chr11:63604419..63605581-chr11:63639188..63640136,5	K562	blood:
22	chr11:63604047..63606273-chr11:63618299..63619902,2	K562	blood:
23	chr11:63604695..63605339-chr11:63920239..63921053,3	K562	blood:
24	chr11:63603344..63615182-chr11:63634321..63647771,46	MCF-7	breast:
25	chr11:63604405..63605358-chr11:63712971..63713992,6	K562	blood:
26	chr11:63604847..63605359-chr11:63915839..63916701,2	K562	blood:
27	chr11:63601754..63603503-chr11:63603668..63606270,2	K562	blood:
28	chr11:63604248..63606622-chr11:63634947..63637040,3	K562	blood:
29	chr11:63604437..63605387-chr11:63701185..63702224,4	MCF-7	breast:
30	chr11:63605094..63609854-chr11:63611414..63617957,11	K562	blood:
31	chr11:63579552..63583589-chr11:63604564..63608557,6	K562	blood:
32	chr11:63604403..63605521-chr11:63639170..63640537,5	MCF-7	breast:
33	chr11:63604392..63605337-chr11:63683573..63684540,2	K562	blood:
34	chr11:63536047..63538392-chr11:63603133..63607498,3	MCF-7	breast:

Variant related genes	Relation type
MARK2	TF binding region
ENSG00000256280	TF binding region
ENSG00000072518	Chromatin interaction
ENSG00000255651	Chromatin interaction
ENSG00000168005	Chromatin interaction
ENSG00000110583	Chromatin interaction
ENSG00000256280	Chromatin interaction
ENSG00000167771	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10736731	0.96[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10751001	0.83[ASN][1000 genomes]
rs10792422	0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10792423	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10897452	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10897453	0.87[ASW][hapmap];0.96[CEU][hapmap];0.85[CHB][hapmap];0.86[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];0.83[MKK][hapmap];0.95[TSI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10897454	0.87[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.83[MKK][hapmap];0.98[TSI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11231600	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11231606	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11231624	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11231628	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11231637	1.00[CEU][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.90[EUR][1000 genomes]
rs11231640	0.92[ASW][hapmap];0.89[CEU][hapmap];0.81[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.89[MEX][hapmap];0.95[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11605500	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12277481	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12576275	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1486936	1.00[CEU][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.90[EUR][1000 genomes]
rs1872772	1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2840079	0.89[CEU][hapmap];0.90[JPT][hapmap];0.88[LWK][hapmap];0.89[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs320109	1.00[CEU][hapmap];0.89[MEX][hapmap];0.93[TSI][hapmap];0.90[EUR][1000 genomes]
rs3802941	0.92[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[LWK][hapmap];0.89[MEX][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3850943	0.83[ASN][1000 genomes]
rs4143327	0.90[EUR][1000 genomes]
rs4963433	0.83[ASN][1000 genomes]
rs4980503	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4980505	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4980507	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4980528	1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4980529	1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4980532	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4980533	0.81[ASW][hapmap];0.92[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61604723	0.85[EUR][1000 genomes]
rs6421686	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6591825	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.94[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7102006	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7105288	1.00[CEU][hapmap];0.94[MEX][hapmap];0.95[TSI][hapmap];0.90[EUR][1000 genomes]
rs7108375	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7110843	0.81[ASW][hapmap];0.96[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.94[MEX][hapmap];0.81[MKK][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7118913	1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.94[MEX][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7121067	0.83[EUR][1000 genomes]
rs7937314	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7939351	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7944519	0.87[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7946503	0.85[EUR][1000 genomes]
rs7948656	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs923247	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs928948	1.00[JPT][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10792421	NAALADL1	cis	cerebellum	SCAN
rs10792421	ZBTB3	cis	parietal	SCAN
rs10792421	DPF2	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63590800-63605200	Weak transcription	Small Intestine	intestine
2	chr11:63593000-63605200	Weak transcription	NHDF-Ad	bronchial
3	chr11:63593000-63606400	Weak transcription	Aorta	Aorta
4	chr11:63594000-63605600	Weak transcription	HSMMtube	muscle
5	chr11:63594200-63605200	Weak transcription	NH-A	brain
6	chr11:63594200-63605600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:63594400-63605400	Weak transcription	HSMM	muscle
8	chr11:63594400-63605400	Weak transcription	Osteobl	bone
9	chr11:63594600-63606400	Weak transcription	Ovary	ovary
10	chr11:63595400-63605200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr11:63595400-63605200	Weak transcription	Left Ventricle	heart
12	chr11:63595400-63605400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:63595600-63605400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr11:63596000-63605200	Weak transcription	Right Ventricle	heart
15	chr11:63596400-63605200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr11:63596600-63605600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:63596800-63605400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:63596800-63605800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:63597200-63605200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:63598400-63605600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:63600400-63605800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr11:63600600-63605200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:63602400-63605600	Enhancers	Adipose Nuclei	Adipose
24	chr11:63603000-63605200	Weak transcription	Esophagus	oesophagus
25	chr11:63603600-63605200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr11:63603800-63605800	Enhancers	Brain Germinal Matrix	brain
27	chr11:63604400-63605200	Enhancers	Hela-S3	cervix
28	chr11:63604400-63605600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:63604400-63605600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:63604400-63605600	Enhancers	Colonic Mucosa	Colon
31	chr11:63604400-63605600	Enhancers	Fetal Intestine Large	intestine
32	chr11:63604400-63605800	Enhancers	Primary B cells from peripheral blood	blood
33	chr11:63604400-63605800	Enhancers	Brain Anterior Caudate	brain
34	chr11:63604400-63605800	Enhancers	Fetal Intestine Small	intestine
35	chr11:63604400-63605800	Enhancers	Gastric	stomach
36	chr11:63604600-63605200	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr11:63604600-63605200	Enhancers	Fetal Brain Female	brain
38	chr11:63604600-63605200	Enhancers	NHEK	skin
39	chr11:63604600-63605400	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr11:63604600-63605400	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr11:63604600-63605400	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr11:63604600-63605600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr11:63604600-63605600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr11:63604600-63605600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr11:63604600-63605600	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr11:63604600-63605600	Enhancers	Colon Smooth Muscle	Colon
47	chr11:63604600-63605600	Enhancers	Right Atrium	heart
48	chr11:63604600-63605600	Enhancers	HMEC	breast
49	chr11:63604600-63605600	Enhancers	K562	blood
50	chr11:63604600-63605800	Enhancers	H9 Cell Line	embryonic stem cell

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