Variant report

Variant	rs589556
Chromosome Location	chr11:64646842-64646843
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:179)
CpG islands
(count:0)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:179 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr11:64645366-64646911	ECC-1	luminal epithelium:	n/a	n/a
2	POLR2A	chr11:64645536-64647176	HL-60	blood:	n/a	n/a
3	CUX1	chr11:64645971-64647098	GM12878	blood:	n/a	n/a
4	TBP	chr11:64645883-64646983	HepG2	liver:	n/a	n/a
5	MAX	chr11:64645323-64646944	HepG2	liver:	n/a	n/a
6	POLR2A	chr11:64645829-64646928	MCF10A-Er-Src	breast:	n/a	n/a
7	BHLHE40	chr11:64645790-64647065	GM12878	blood:	n/a	n/a
8	HA-E2F1	chr11:64645721-64646904	MCF-7	breast:	n/a	chr11:64646050-64646059
9	POLR2A	chr11:64645802-64647273	K562	blood:	n/a	n/a
10	RELA	chr11:64645778-64647276	GM12891	blood:	n/a	chr11:64646925-64646934 chr11:64646925-64646934
11	REST	chr11:64645604-64646855	A549	lung:	n/a	n/a
12	RCOR1	chr11:64644050-64647190	IMR90	lung:	n/a	n/a
13	PBX3	chr11:64645782-64647253	A549	lung:	n/a	n/a
14	POLR2A	chr11:64645936-64647536	K562	blood:	n/a	n/a
15	MYC	chr11:64645499-64646918	K562	blood:	n/a	n/a
16	POLR2A	chr11:64645734-64647588	HCT-116	colon:	n/a	n/a
17	MAX	chr11:64645346-64647079	A549	lung:	n/a	n/a
18	TAF1	chr11:64646228-64646857	K562	blood:	n/a	n/a
19	HEY1	chr11:64645678-64646912	K562	blood:	n/a	n/a
20	RELA	chr11:64645692-64647595	GM18505	blood:	n/a	chr11:64646925-64646934 chr11:64646925-64646934
21	MAX	chr11:64645345-64647043	HepG2	liver:	n/a	n/a
22	MAX	chr11:64645564-64646925	NB4	blood:	n/a	n/a
23	POLR2A	chr11:64644259-64646897	ProgFib	skin:	n/a	n/a
24	TBP	chr11:64645698-64647295	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:64646752-64647090	GM12891	blood:	n/a	n/a
26	POU2F2	chr11:64645417-64647252	GM12878	blood:	n/a	n/a
27	MYC	chr11:64645763-64646935	NB4	blood:	n/a	n/a
28	SPI1	chr11:64646714-64647116	GM12878	blood:	n/a	chr11:64647011-64647024 chr11:64646874-64646887 chr11:64646913-64646922 chr11:64646986-64646999
29	POLR2A	chr11:64644871-64648628	Raji	blood:	n/a	n/a
30	POLR2A	chr11:64645676-64647115	MCF10A-Er-Src	breast:	n/a	n/a
31	MXI1	chr11:64644376-64647063	GM12878	blood:	n/a	n/a
32	POLR2A	chr11:64645563-64647145	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr11:64645792-64647779	PFSK-1	brain:	n/a	n/a
34	POLR2A	chr11:64643014-64646953	GM12878	blood:	n/a	n/a
35	CREB1	chr11:64645741-64647163	GM12878	blood:	n/a	n/a
36	MTA3	chr11:64642909-64647630	GM12878	blood:	n/a	n/a
37	MXI1	chr11:64642996-64647031	IMR90	lung:	n/a	n/a
38	POLR2A	chr11:64645364-64647142	GM18526	blood:	n/a	n/a
39	POLR2A	chr11:64644306-64647272	GM19193	blood:	n/a	n/a
40	POLR2A	chr11:64645396-64646984	ECC-1	luminal epithelium:	n/a	n/a
41	NFATC1	chr11:64645679-64647077	GM12878	blood:	n/a	n/a
42	SPI1	chr11:64646653-64647533	HL-60	blood:	n/a	chr11:64647011-64647024 chr11:64646874-64646887 chr11:64646913-64646922 chr11:64647387-64647394 chr11:64646986-64646999
43	SP1	chr11:64646810-64647128	GM12878	blood:	n/a	n/a
44	MAX	chr11:64645376-64646969	K562	blood:	n/a	n/a
45	RUNX3	chr11:64645558-64647378	GM12878	blood:	n/a	n/a
46	MAZ	chr11:64643035-64647566	IMR90	lung:	n/a	n/a
47	CHD1	chr11:64641789-64647512	IMR90	lung:	n/a	n/a
48	WRNIP1	chr11:64646675-64647487	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:64645661-64647407	HCT-116	colon:	n/a	n/a
50	MXI1	chr11:64644051-64647757	SK-N-SH	brain:	n/a	n/a

No data

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64644496..64646920-chr11:64764507..64767051,3	K562	blood:
2	chr11:64576838..64579724-chr11:64644602..64648695,4	K562	blood:
3	chr11:64643787..64646984-chr11:64875593..64882466,11	MCF-7	breast:
4	chr11:64645037..64647722-chr11:64889185..64892415,3	MCF-7	breast:
5	chr11:64644179..64646943-chr11:64683100..64687957,8	MCF-7	breast:
6	chr11:64645458..64648042-chr11:64679788..64682013,2	MCF-7	breast:
7	chr11:64645500..64648132-chr11:64701780..64703587,2	MCF-7	breast:
8	chr11:64566980..64568493-chr11:64644627..64647594,2	MCF-7	breast:
9	chr11:64506827..64509728-chr11:64644773..64647136,2	K562	blood:
10	chr11:64645266..64647348-chr11:64764267..64766007,3	K562	blood:
11	chr11:64543733..64546506-chr11:64646290..64648884,3	K562	blood:
12	chr11:64644621..64647085-chr11:64869842..64873650,4	MCF-7	breast:
13	chr11:64643788..64647961-chr11:64848883..64851896,4	K562	blood:
14	chr11:64644806..64648507-chr11:64877927..64882201,4	MCF-7	breast:
15	chr11:64643878..64648186-chr11:64793107..64797470,5	K562	blood:
16	chr11:64598378..64602131-chr11:64643786..64647178,3	K562	blood:
17	chr11:64568225..64570801-chr11:64644714..64647592,2	MCF-7	breast:
18	chr11:64578009..64579724-chr11:64644602..64647037,2	K562	blood:
19	chr11:64543733..64546227-chr11:64645757..64648257,3	K562	blood:
20	chr11:64643590..64647956-chr11:64883297..64887661,6	MCF-7	breast:
21	chr11:64646527..64648346-chr11:64683617..64685265,2	MCF-7	breast:
22	chr11:64644503..64648099-chr11:64683052..64686363,9	K562	blood:
23	chr11:64644475..64647391-chr11:64946794..64949864,4	K562	blood:
24	chr11:64644499..64647040-chr17:57916781..57919732,2	MCF-7	breast:
25	chr11:64642261..64647543-chr11:64882719..64886329,5	MCF-7	breast:
26	chr11:64645160..64647408-chr11:65080658..65083337,2	MCF-7	breast:
27	chr11:64644921..64647626-chr11:64948017..64950319,4	K562	blood:
28	chr11:64646646..64648212-chr11:64949732..64952705,2	MCF-7	breast:
29	chr11:64645625..64647922-chr11:64900749..64903645,2	MCF-7	breast:
30	chr11:64645854..64647856-chr11:64806233..64808621,2	K562	blood:
31	chr11:64644663..64647408-chr11:64807363..64809566,4	MCF-7	breast:
32	chr11:64644628..64647764-chr11:64688767..64693294,4	K562	blood:
33	chr11:64644760..64647431-chr11:64850066..64853139,4	K562	blood:
34	chr11:64644764..64647368-chr11:64690531..64692792,2	K562	blood:
35	chr11:64545301..64547974-chr11:64645436..64647559,2	MCF-7	breast:
36	chr11:64644835..64647462-chr11:64855986..64857500,2	MCF-7	breast:
37	chr11:64642873..64648975-chr11:64779425..64783727,9	MCF-7	breast:
38	chr11:64644462..64647222-chr11:64847025..64851524,4	MCF-7	breast:
39	chr11:64646046..64648742-chr11:64862657..64865181,3	K562	blood:

No data

Variant related genes	Relation type
EHD1	TF binding region
ENSG00000230835	TF binding region
ENSG00000149806	Chromatin interaction
ENSG00000149798	Chromatin interaction
ENSG00000168062	Chromatin interaction
ENSG00000149823	Chromatin interaction
ENSG00000254614	Chromatin interaction
ENSG00000149809	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000168066	Chromatin interaction
ENSG00000270775	Chromatin interaction
ENSG00000133895	Chromatin interaction
ENSG00000171219	Chromatin interaction
ENSG00000110046	Chromatin interaction
ENSG00000254501	Chromatin interaction
ENSG00000149792	Chromatin interaction
ENSG00000162300	Chromatin interaction
ENSG00000273003	Chromatin interaction
ENSG00000174276	Chromatin interaction
ENSG00000068831	Chromatin interaction
ENSG00000168061	Chromatin interaction
ENSG00000110025	Chromatin interaction
ENSG00000269038	Chromatin interaction
ENSG00000213465	Chromatin interaction
ENSG00000014216	Chromatin interaction
ENSG00000146670	Chromatin interaction
ENSG00000187066	Chromatin interaction
ENSG00000168067	Chromatin interaction
ENSG00000255173	Chromatin interaction
ENSG00000068971	Chromatin interaction
ENSG00000162298	Chromatin interaction
ENSG00000149735	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10897533	0.91[CHB][hapmap];0.82[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs1211284	0.91[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12573	0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs12801172	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17146413	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2007521	0.92[ASN][1000 genomes]
rs2077026	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3741391	0.90[ASN][1000 genomes]
rs3893108	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3936999	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs3937000	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs41381745	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4930280	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4930281	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4930685	0.91[CHB][hapmap];0.98[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs57851864	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs602347	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs607569	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs620066	0.86[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs621608	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs622611	0.91[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs635722	0.94[ASN][1000 genomes]
rs641623	0.98[ASN][1000 genomes]
rs649208	0.88[ASN][1000 genomes]
rs653225	0.91[ASN][1000 genomes]
rs654580	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs656982	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7126744	0.94[ASN][1000 genomes]
rs7926812	0.94[ASN][1000 genomes]
rs7927560	0.90[ASN][1000 genomes]
rs7943238	0.88[ASN][1000 genomes]
rs7944276	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7949887	0.81[CHB][hapmap];0.82[ASN][1000 genomes]
rs7952306	0.93[ASN][1000 genomes]
rs7952567	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
2	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
3	nsv897700	chr11:64447420-64701030	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1071 gene(s)	inside rSNPs	diseases
4	nsv897704	chr11:64584987-64701030	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1028 gene(s)	inside rSNPs	diseases
5	nsv897705	chr11:64591679-64701030	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1028 gene(s)	inside rSNPs	diseases
6	nsv897706	chr11:64591679-64721908	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1028 gene(s)	inside rSNPs	diseases
7	nsv897707	chr11:64600002-64701030	Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1028 gene(s)	inside rSNPs	diseases
8	nsv897708	chr11:64602757-64695271	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1028 gene(s)	inside rSNPs	diseases
9	nsv360	chr11:64632395-64659636	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1003 gene(s)	inside rSNPs	diseases
10	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers 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 miRNA miRNA target site	1539 gene(s)	inside rSNPs	diseases
11	nsv555208	chr11:64645119-64771179	Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1029 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64643400-64647000	Active TSS	Aorta	Aorta
2	chr11:64643800-64647200	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr11:64644200-64647000	Active TSS	Duodenum Smooth Muscle	Duodenum
4	chr11:64644400-64647000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:64644400-64647000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:64644400-64647000	Active TSS	Colon Smooth Muscle	Colon
7	chr11:64644800-64647000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr11:64644800-64647000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:64644800-64647000	Active TSS	Left Ventricle	heart
10	chr11:64644800-64647400	Active TSS	H9 Cell Line	embryonic stem cell
11	chr11:64645000-64647000	Active TSS	Ovary	ovary
12	chr11:64645200-64647000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:64645200-64647000	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr11:64645200-64647000	Active TSS	Psoas Muscle	Psoas
15	chr11:64645200-64647200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:64645200-64647200	Active TSS	Fetal Kidney	kidney
17	chr11:64645400-64647000	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr11:64645400-64647000	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr11:64645400-64647200	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr11:64645400-64647400	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr11:64645600-64647000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:64645600-64647400	Active TSS	H1 Cell Line	embryonic stem cell
23	chr11:64646200-64647400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr11:64646200-64647600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr11:64646400-64647000	Flanking Active TSS	Primary B cells from peripheral blood	blood
26	chr11:64646400-64647000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:64646400-64647000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr11:64646400-64647000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
29	chr11:64646400-64647000	Flanking Active TSS	Fetal Lung	lung
30	chr11:64646400-64647000	Flanking Active TSS	NH-A	brain
31	chr11:64646400-64647200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr11:64646400-64647200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
33	chr11:64646400-64647200	Flanking Active TSS	Colonic Mucosa	Colon
34	chr11:64646400-64647200	Flanking Active TSS	Fetal Muscle Trunk	muscle
35	chr11:64646400-64647200	Flanking Active TSS	Fetal Thymus	thymus
36	chr11:64646400-64647200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr11:64646400-64647200	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr11:64646400-64647200	Flanking Active TSS	HSMMtube	muscle
39	chr11:64646400-64647200	Flanking Active TSS	HUVEC	blood vessel
40	chr11:64646400-64647200	Flanking Active TSS	Osteobl	bone
41	chr11:64646400-64647400	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr11:64646400-64647400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr11:64646400-64647400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:64646400-64647400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr11:64646400-64647400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:64646400-64647400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr11:64646400-64647600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
48	chr11:64646400-64647600	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr11:64646400-64647600	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr11:64646400-64648600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood

The 2.0 version of rSNPBase

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