Variant report

Variant	rs320155
Chromosome Location	chr11:63768214-63768215
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	CTCF	chr11:63767832-63768322	H1-hESC	embryonic stem cell:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
2	POLR2A	chr11:63765985-63768345	GM12878	blood:	n/a	n/a
3	RAD21	chr11:63767813-63768293	H1-hESC	embryonic stem cell:	n/a	chr11:63768050-63768069 chr11:63768055-63768065
4	POLR2A	chr11:63767102-63768465	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:63768132-63768221	GM12878	blood:	n/a	n/a
6	POLR2A	chr11:63768085-63768863	GM12891	blood:	n/a	n/a
7	POLR2A	chr11:63763487-63769382	K562	blood:	n/a	n/a
8	CTCF	chr11:63768100-63768250	GM12801	blood:	n/a	n/a
9	ELF1	chr11:63768012-63768326	K562	blood:	n/a	chr11:63768129-63768141 chr11:63768252-63768264
10	ELF1	chr11:63767536-63768367	GM12878	blood:	n/a	chr11:63768129-63768141 chr11:63768252-63768264 chr11:63767949-63767961 chr11:63767943-63767955
11	ZNF143	chr11:63767888-63768245	GM12878	blood:	n/a	n/a
12	MTA3	chr11:63768098-63768469	GM12878	blood:	n/a	n/a
13	ELF1	chr11:63767787-63768369	GM12878	blood:	n/a	chr11:63768129-63768141 chr11:63768252-63768264 chr11:63767949-63767961 chr11:63767943-63767955
14	ZNF143	chr11:63767905-63768514	H1-hESC	embryonic stem cell:	n/a	chr11:63768246-63768256
15	POLR2A	chr11:63767675-63768494	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr11:63768009-63768354	K562	blood:	n/a	n/a
17	POLR2A	chr11:63767955-63768796	GM12892	blood:	n/a	n/a
18	POLR2A	chr11:63768046-63768280	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr11:63767814-63768312	H1-hESC	embryonic stem cell:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
20	POLR2A	chr11:63768046-63768903	PANC-1	pancreas:	n/a	n/a
21	YY1	chr11:63767870-63768233	GM12892	blood:	n/a	chr11:63768090-63768104 chr11:63767941-63767955 chr11:63767948-63767962 chr11:63768092-63768101 chr11:63768055-63768069 chr11:63768132-63768143 chr11:63767953-63767964 chr11:63767947-63767961 chr11:63768087-63768101
22	RAD21	chr11:63767938-63768298	A549	lung:	n/a	chr11:63768050-63768069 chr11:63768055-63768065
23	POLR2A	chr11:63768192-63768432	GM12891	blood:	n/a	n/a
24	BCLAF1	chr11:63767874-63768219	GM12878	blood:	n/a	chr11:63767947-63767960 chr11:63767943-63767956 chr11:63767949-63767962 chr11:63767950-63767963 chr11:63768128-63768141
25	SMC3	chr11:63767896-63768242	GM12878	blood:	n/a	chr11:63768055-63768065 chr11:63768051-63768065
26	CTCF	chr11:63767849-63768259	GM12878	blood:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
27	YY1	chr11:63767893-63768247	GM12891	blood:	n/a	chr11:63768090-63768104 chr11:63767941-63767955 chr11:63767948-63767962 chr11:63768092-63768101 chr11:63768055-63768069 chr11:63768132-63768143 chr11:63767953-63767964 chr11:63767947-63767961 chr11:63768087-63768101
28	TAF7	chr11:63767959-63768263	H1-hESC	embryonic stem cell:	n/a	n/a
29	RAD21	chr11:63767841-63768311	IMR90	lung:	n/a	chr11:63768050-63768069 chr11:63768055-63768065
30	POLR2A	chr11:63767588-63768318	GM18951	blood:	n/a	n/a
31	MAZ	chr11:63767761-63768605	IMR90	lung:	n/a	chr11:63768126-63768136
32	POLR2A	chr11:63767642-63768329	A549	lung:	n/a	n/a
33	CTCF	chr11:63767696-63768262	GM12892	blood:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
34	YY1	chr11:63767884-63768214	GM12878	blood:	n/a	chr11:63768090-63768104 chr11:63767941-63767955 chr11:63767948-63767962 chr11:63768092-63768101 chr11:63768055-63768069 chr11:63768132-63768143 chr11:63767953-63767964 chr11:63767947-63767961 chr11:63768087-63768101
35	TBP	chr11:63768017-63768245	H1-hESC	embryonic stem cell:	n/a	n/a
36	PAX5	chr11:63767924-63768403	GM12892	blood:	n/a	chr11:63767996-63768023
37	CHD2	chr11:63768043-63768260	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr11:63767806-63768260	IMR90	lung:	n/a	n/a
39	POLR2A	chr11:63765335-63768311	GM12878	blood:	n/a	n/a
40	CTCF	chr11:63767698-63768226	GM19238	blood:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
41	ZNF263	chr11:63768063-63768474	HEK293-T-REx	kidney:	n/a	chr11:63768180-63768189
42	SIN3A	chr11:63767682-63768219	H1-hESC	embryonic stem cell:	n/a	chr11:63767864-63767877
43	POLR2A	chr11:63768190-63771259	PFSK-1	brain:	n/a	n/a
44	CTCF	chr11:63767888-63768278	Spleen_OC	spleen:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
45	POLR2A	chr11:63768086-63768440	GM12891	blood:	n/a	n/a
46	CTCF	chr11:63767790-63768326	A549	lung:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
47	CCNT2	chr11:63768203-63768343	K562	blood:	n/a	n/a
48	POLR2A	chr11:63765309-63768451	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:63765114-63768623	SK-N-MC	brain:	n/a	n/a
50	CTCF	chr11:63767897-63768234	GM12891	blood:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065

No.	Distal block	Cell Line	Cell type
1	chr11:63740468..63742451-chr11:63765485..63768295,3	K562	blood:
2	chr11:63766001..63768236-chr11:63932252..63933831,2	MCF-7	breast:
3	chr11:63766704..63768642-chr11:63953085..63955113,2	MCF-7	breast:
4	chr11:63767743..63768450-chr16:50186380..50187229,2	NB4	blood:
5	chr11:63765241..63769899-chr11:63951624..63954334,5	MCF-7	breast:
6	chr11:63752288..63756029-chr11:63763681..63768717,11	MCF-7	breast:

Variant related genes	Relation type
OTUB1	TF binding region
MACROD1	TF binding region
ENSG00000256100	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000167770	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000121274	Chromatin interaction
ENSG00000133315	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs167658	1.00[AMR][1000 genomes]
rs320150	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320151	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320157	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs320158	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59114361	1.00[AMR][1000 genomes]
rs7113021	1.00[AMR][1000 genomes]
rs7117821	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 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	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv897629	chr11:63664882-63866959	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription 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	43 gene(s)	inside rSNPs	diseases
5	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS 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
6	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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	254 gene(s)	inside rSNPs	diseases
7	nsv897639	chr11:63691049-63844683	Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	esv1849906	chr11:63719273-63880383	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv1042075	chr11:63732454-63813164	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	esv29993	chr11:63738642-63864211	Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer 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 miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv897640	chr11:63744152-63835611	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
12	nsv897641	chr11:63744152-63844683	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv897642	chr11:63744152-63866959	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
14	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
15	nsv897643	chr11:63754986-63844683	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
16	nsv897644	chr11:63754986-63849330	Bivalent Enhancer Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
17	nsv897645	chr11:63754986-63859751	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription 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	19 gene(s)	inside rSNPs	diseases
18	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS 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	245 gene(s)	inside rSNPs	diseases
19	nsv897647	chr11:63755961-63835611	Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
20	nsv897648	chr11:63761169-63774370	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
21	nsv897649	chr11:63761169-63844683	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking 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	11 gene(s)	inside rSNPs	diseases
22	nsv897650	chr11:63761169-63849330	Bivalent Enhancer Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
23	nsv897651	chr11:63761169-63863405	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
24	nsv897652	chr11:63761169-63866959	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
25	nsv897653	chr11:63761169-63875456	Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
26	esv3340630	chr11:63766801-63769349	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63755000-63769000	Weak transcription	Fetal Kidney	kidney
2	chr11:63755200-63775200	Weak transcription	Psoas Muscle	Psoas
3	chr11:63756200-63769200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:63759200-63774800	Weak transcription	HSMMtube	muscle
5	chr11:63760600-63771800	Strong transcription	Dnd41	blood
6	chr11:63762600-63777800	Weak transcription	Hela-S3	cervix
7	chr11:63764200-63768400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:63764800-63772000	Weak transcription	HepG2	liver
9	chr11:63765000-63769400	Weak transcription	HSMM	muscle
10	chr11:63765000-63774200	Weak transcription	Brain Angular Gyrus	brain
11	chr11:63766000-63768600	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr11:63766200-63768400	Active TSS	H9 Cell Line	embryonic stem cell
13	chr11:63766200-63768400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:63766200-63768600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
15	chr11:63766400-63770200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr11:63766400-63770400	Enhancers	Fetal Heart	heart
17	chr11:63766400-63770600	Enhancers	Placenta	Placenta
18	chr11:63766600-63768600	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr11:63766800-63768400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:63766800-63768400	Enhancers	Gastric	stomach
21	chr11:63766800-63768800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:63766800-63768800	Enhancers	HMEC	breast
23	chr11:63766800-63769000	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr11:63766800-63770400	Enhancers	Lung	lung
25	chr11:63767000-63768400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr11:63767000-63768600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr11:63767000-63768800	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr11:63767000-63774400	Weak transcription	K562	blood
29	chr11:63767200-63768400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
30	chr11:63767200-63768400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr11:63767200-63768400	Enhancers	Small Intestine	intestine
32	chr11:63767200-63768600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr11:63767200-63768600	Bivalent Enhancer	Stomach Mucosa	stomach
34	chr11:63767200-63769800	Enhancers	Liver	Liver
35	chr11:63767200-63769800	Enhancers	Brain Anterior Caudate	brain
36	chr11:63767200-63770200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr11:63767400-63768400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
38	chr11:63767400-63768400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
39	chr11:63767400-63768400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:63767400-63768600	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr11:63767400-63768600	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr11:63767400-63768600	Flanking Active TSS	Colonic Mucosa	Colon
43	chr11:63767600-63768400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:63767600-63768400	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
45	chr11:63767600-63768400	Active TSS	Right Atrium	heart
46	chr11:63767600-63768800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr11:63767600-63768800	Weak transcription	Fetal Lung	lung
48	chr11:63767800-63768400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:63767800-63768400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:63767800-63768400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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