Variant report

Variant	rs4970988
Chromosome Location	chr1:150950062-150950063
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	BHLHE40	chr1:150949195-150950106	K562	blood:	n/a	n/a
2	POLR2A	chr1:150949755-150950162	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr1:150949728-150950135	A549	lung:	n/a	n/a
4	POLR2A	chr1:150949709-150950267	Hela-S3	cervix:	n/a	n/a
5	JUND	chr1:150949815-150950088	H1-hESC	embryonic stem cell:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949986-150949997 chr1:150949987-150949997 chr1:150950040-150950054
6	ETS1	chr1:150949621-150950098	K562	blood:	n/a	chr1:150949995-150950002 chr1:150949991-150950006 chr1:150949699-150949712 chr1:150949991-150950002 chr1:150949989-150950003
7	EP300	chr1:150949832-150950077	HepG2	liver:	n/a	n/a
8	MYC	chr1:150949762-150950107	MCF-7	breast:	n/a	n/a
9	MXI1	chr1:150949694-150950142	HepG2	liver:	n/a	n/a
10	MAZ	chr1:150949345-150950151	K562	blood:	n/a	n/a
11	MYC	chr1:150949387-150950151	K562	blood:	n/a	n/a
12	POLR2A	chr1:150949639-150950281	Hela-S3	cervix:	n/a	n/a
13	HEY1	chr1:150949661-150950248	HepG2	liver:	n/a	n/a
14	GABPA	chr1:150949695-150950104	K562	blood:	n/a	n/a
15	TCF7L2	chr1:150949809-150950117	Hela-S3	cervix:	n/a	chr1:150949987-150949996
16	MAX	chr1:150949068-150950119	K562	blood:	n/a	n/a
17	TEAD4	chr1:150949811-150950091	H1-hESC	embryonic stem cell:	n/a	n/a
18	JUND	chr1:150949843-150950097	HepG2	liver:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949986-150949997 chr1:150949987-150949997 chr1:150950040-150950054
19	EP300	chr1:150949759-150950140	Hela-S3	cervix:	n/a	n/a
20	HEY1	chr1:150949128-150950179	K562	blood:	n/a	n/a
21	POLR2A	chr1:150948639-150950133	K562	blood:	n/a	n/a
22	SPI1	chr1:150949488-150950308	HL-60	blood:	n/a	chr1:150949996-150950003 chr1:150949699-150949712
23	POLR2A	chr1:150949741-150950069	H1-hESC	embryonic stem cell:	n/a	n/a
24	YY1	chr1:150949829-150950218	H1-hESC	embryonic stem cell:	n/a	n/a
25	SP1	chr1:150949170-150950418	HCT-116	colon:	n/a	chr1:150949692-150949705 chr1:150949950-150949960 chr1:150949950-150949960
26	BCLAF1	chr1:150949514-150950125	K562	blood:	n/a	n/a
27	JUN	chr1:150949372-150950424	K562	blood:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949987-150949997 chr1:150950040-150950054
28	FOSL1	chr1:150949348-150950328	HCT-116	colon:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949987-150949997 chr1:150950040-150950054
29	JUND	chr1:150949481-150950426	HCT-116	colon:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949986-150949997 chr1:150949987-150949997 chr1:150950040-150950054
30	POLR2A	chr1:150949600-150950259	SK-N-SH	brain:	n/a	n/a
31	SMARCB1	chr1:150949690-150950350	Hela-S3	cervix:	n/a	n/a
32	YY1	chr1:150949774-150950098	HCT-116	colon:	n/a	n/a
33	IRF1	chr1:150948650-150950171	K562	blood:	n/a	chr1:150949992-150950001 chr1:150949947-150949961
34	FOS	chr1:150949803-150950171	MCF10A-Er-Src	breast:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949986-150949997 chr1:150950040-150950054
35	SP1	chr1:150949534-150950412	A549	lung:	n/a	chr1:150949692-150949705 chr1:150949950-150949960 chr1:150949950-150949960
36	POLR2A	chr1:150949777-150950111	ProgFib	skin:	n/a	n/a
37	SP1	chr1:150949642-150950221	H1-hESC	embryonic stem cell:	n/a	chr1:150949692-150949705 chr1:150949950-150949960 chr1:150949950-150949960
38	FOSL2	chr1:150949705-150950208	HepG2	liver:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949985-150949996 chr1:150949987-150949997 chr1:150950040-150950054
39	EBF1	chr1:150949784-150950072	GM12878	blood:	n/a	n/a
40	GABPA	chr1:150949716-150950227	A549	lung:	n/a	n/a
41	ZKSCAN1	chr1:150949784-150950164	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr1:150949401-150950218	K562	blood:	n/a	n/a
43	MAX	chr1:150949727-150950160	Hela-S3	cervix:	n/a	n/a
44	TBL1XR1	chr1:150949244-150950095	K562	blood:	n/a	n/a
45	JUND	chr1:150949720-150950185	A549	lung:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949986-150949997 chr1:150949987-150949997 chr1:150950040-150950054
46	CCNT2	chr1:150949295-150950324	K562	blood:	n/a	chr1:150949739-150949759
47	MAX	chr1:150949651-150950295	A549	lung:	n/a	n/a
48	POLR2A	chr1:150949713-150950216	ECC-1	luminal epithelium:	n/a	n/a
49	JUND	chr1:150949759-150950158	HepG2	liver:	n/a	chr1:150949987-150949997 chr1:150949987-150949997 chr1:150949986-150949997 chr1:150949987-150949997 chr1:150950040-150950054
50	POLR2A	chr1:150949739-150950121	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:150550324..150553500-chr1:150948263..150951593,4	MCF-7	breast:
2	chr1:150949758..150950303-chr1:150978331..150979146,2	K562	blood:
3	chr1:150949558..150951518-chr1:150957213..150958786,2	K562	blood:
4	chr1:150897410..150900366-chr1:150947492..150952156,4	K562	blood:
5	chr1:150949543..150951625-chr11:11620473..11621993,2	MCF-7	breast:
6	chr1:150950044..150951710-chr4:104823461..104824979,2	MCF-7	breast:
7	chr1:150949479..150950097-chr20:56964168..56964788,2	Hela-S3	cervix:
8	chr1:150948646..150951124-chr1:150967629..150969757,2	K562	blood:
9	chr1:150949968..150951775-chr4:104823480..104824982,3	MCF-7	breast:
10	chr1:150948448..150951342-chr1:151016605..151018874,2	K562	blood:
11	chr1:150948791..150950437-chr17:56735372..56737821,2	MCF-7	breast:
12	chr1:150949418..150950356-chr17:39844321..39845262,2	Hela-S3	cervix:
13	chr1:150949753..150950498-chr12:46766172..46766936,2	NB4	blood:
14	chr1:150520324..150522575-chr1:150949260..150951135,2	K562	blood:
15	chr1:150892976..150894840-chr1:150949265..150951717,2	K562	blood:
16	chr1:150205150..150208917-chr1:150946080..150950396,4	MCF-7	breast:
17	chr1:150898449..150900113-chr1:150949703..150951359,2	MCF-7	breast:

Variant related genes	Relation type
CERS2	TF binding region
ANXA9	TF binding region
ENSG00000143379	Chromatin interaction
ENSG00000143382	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000163141	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000134294	Chromatin interaction
ENSG00000225996	Chromatin interaction
ENSG00000143409	Chromatin interaction
ENSG00000173812	Chromatin interaction
ENSG00000143401	Chromatin interaction
ENSG00000124164	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 27 )

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10305704	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs10305711	0.96[CEU][hapmap];0.93[TSI][hapmap]
rs10305714	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs10399947	0.80[EUR][1000 genomes]
rs10888397	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10888398	0.88[CEU][hapmap];0.95[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap];0.82[ASN][1000 genomes]
rs11204739	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11204742	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11204743	0.84[ASN][1000 genomes]
rs11204747	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11204748	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11204749	0.90[CHB][hapmap];0.84[JPT][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11204750	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11552229	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs11579736	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11581757	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11583707	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11589886	0.82[ASN][1000 genomes]
rs12059949	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12067685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12085336	0.88[CEU][hapmap]
rs12090215	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12096831	0.87[CHB][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12097963	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12119409	0.85[CHB][hapmap]
rs12141871	0.85[CHB][hapmap]
rs12145224	0.86[CHB][hapmap];0.81[CHD][hapmap]
rs12405726	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12409208	1.00[CEU][hapmap];0.87[CHB][hapmap];0.82[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12410394	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12410869	0.88[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap]
rs12562939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1546376	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1889740	0.88[CEU][hapmap];0.81[TSI][hapmap]
rs1889741	0.88[CEU][hapmap];0.91[CHB][hapmap];0.84[CHD][hapmap];0.84[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap]
rs1972060	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2004903	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2124952	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2228099	0.88[CEU][hapmap];0.81[TSI][hapmap]
rs2256355	0.87[CEU][hapmap];0.81[TSI][hapmap]
rs2271076	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2272214	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2280627	0.88[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2864873	0.88[CEU][hapmap];0.81[TSI][hapmap]
rs2864882	0.82[ASN][1000 genomes]
rs2867296	0.85[EUR][1000 genomes]
rs34985895	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3738478	0.81[CHD][hapmap]
rs3768013	0.88[CEU][hapmap]
rs3768015	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs3768016	1.00[CEU][hapmap];0.93[TSI][hapmap]
rs3843843	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3849279	0.88[CEU][hapmap];0.87[CHB][hapmap];0.87[CHD][hapmap];0.90[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.81[TSI][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4451553	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.91[TSI][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4509581	0.83[CEU][hapmap]
rs4970928	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4970929	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4970930	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4970931	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4970982	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4970984	0.82[ASN][1000 genomes]
rs4970985	0.82[ASN][1000 genomes]
rs4970986	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4970987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[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]
rs59024312	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6587542	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6658066	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6660845	0.80[EUR][1000 genomes]
rs6664622	0.86[CHB][hapmap]
rs6669855	0.80[EUR][1000 genomes]
rs6677420	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66847267	0.81[ASN][1000 genomes]
rs72704679	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72704682	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72704685	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7518156	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs752376	0.88[CEU][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.88[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7528773	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7532045	0.88[CEU][hapmap];0.81[TSI][hapmap]
rs7548516	0.91[CHB][hapmap];0.89[CHD][hapmap];0.91[YRI][hapmap];0.87[ASN][1000 genomes]
rs7556451	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7556661	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8444	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs897815	1.00[CEU][hapmap];0.95[CHB][hapmap];0.84[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9661876	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001897	chr1:150743271-151241600	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv535158	chr1:150743271-151241600	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv1008496	chr1:150845827-150970656	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
4	nsv522317	chr1:150933723-150974162	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv522840	chr1:150933723-151347746	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	169 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Urate levels	23263486	GWAS catalog

mRNA abundance (count:26)

SNP	Gene	Cis/trans	Tissue	Source
rs4970988	CTSS	cis	Thyroid	GTEx
rs4970988	HORMAD1	cis	Skin Sun Exposed Lower leg	GTEx
rs4970988	RP11-316M1.12	cis	Nerve Tibial	GTEx
rs4970988	RP11-316M1.12	cis	Muscle Skeletal	GTEx
rs4970988	RP11-316M1.12	cis	Adipose Subcutaneous	GTEx
rs4970988	RP11-316M1.12	cis	Artery Aorta	GTEx
rs4970988	GOLPH3L	cis	Nerve Tibial	GTEx
rs4970988	ARNT	cis	normal skin	skin_eQTL
rs4970988	HORMAD1	cis	lesional skin	skin_eQTL
rs4970988	HORMAD1	cis	Nerve Tibial	GTEx
rs4970988	RP11-316M1.12	cis	Thyroid	GTEx
rs4970988	CTSS	cis	Lymphoblastoid	GTEx
rs4970988	HORMAD1	cis	Adipose Subcutaneous	GTEx
rs4970988	RP11-316M1.12	cis	Heart Left Ventricle	GTEx
rs4970988	HORMAD1	cis	Esophagus Mucosa	GTEx
rs4970988	ARNT	cis	multi-tissue	Pritchard
rs4970988	RP11-316M1.12	cis	Esophagus Muscularis	GTEx
rs4970988	RP11-316M1.12	cis	Whole Blood	GTEx
rs4970988	HORMAD1	cis	uninvolved skin	skin_eQTL
rs4970988	CTSS	cis	multi-tissue	Pritchard
rs4970988	RNU6-1042P	cis	Esophagus Mucosa	GTEx
rs4970988	RP11-316M1.12	cis	Artery Tibial	GTEx
rs4970988	RP11-316M1.12	cis	Esophagus Mucosa	GTEx
rs4970988	RP11-316M1.12	cis	lung	GTEx
rs4970988	GOLPH3L	cis	Skin Sun Exposed Lower leg	GTEx
rs4970988	HORMAD1	cis	normal skin	skin_eQTL

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150947800-150950400	Enhancers	Stomach Mucosa	stomach
2	chr1:150947800-150950400	Flanking Active TSS	K562	blood
3	chr1:150947800-150950400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr1:150948000-150950200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:150948000-150950200	Enhancers	Fetal Muscle Leg	muscle
6	chr1:150948000-150950200	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr1:150948000-150950400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:150948000-150950400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:150948000-150950400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
10	chr1:150948000-150950400	Enhancers	NHEK	skin
11	chr1:150948000-150950600	Enhancers	Fetal Thymus	thymus
12	chr1:150948000-150951600	Enhancers	Primary T cells fromperipheralblood	blood
13	chr1:150948000-150951600	Weak transcription	Colonic Mucosa	Colon
14	chr1:150948000-150951600	Enhancers	Fetal Intestine Large	intestine
15	chr1:150948000-150951600	Weak transcription	Fetal Kidney	kidney
16	chr1:150948000-150951600	Weak transcription	Ovary	ovary
17	chr1:150948000-150951800	Weak transcription	Psoas Muscle	Psoas
18	chr1:150948000-150952600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:150948000-150952600	Enhancers	Fetal Intestine Small	intestine
20	chr1:150948200-150950200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:150948200-150950400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr1:150948200-150950600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:150948200-150951400	Weak transcription	Fetal Lung	lung
24	chr1:150948200-150951600	Enhancers	Primary T cells from cord blood	blood
25	chr1:150948200-150951800	Weak transcription	Brain Germinal Matrix	brain
26	chr1:150948200-150952000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:150948400-150950200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr1:150948400-150950200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr1:150948400-150950400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:150948400-150950400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:150948600-150950400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:150948600-150950600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr1:150948600-150950600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:150948600-150951800	Weak transcription	Fetal Brain Female	brain
35	chr1:150948600-150952800	Enhancers	Placenta	Placenta
36	chr1:150948800-150950200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:150948800-150950200	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr1:150948800-150950400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr1:150948800-150950600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr1:150948800-150950600	Enhancers	Stomach Smooth Muscle	stomach
41	chr1:150948800-150952000	Enhancers	Lung	lung
42	chr1:150949000-150951600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr1:150949200-150950200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:150949200-150950200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr1:150949200-150950400	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr1:150949200-150950400	Enhancers	Brain Angular Gyrus	brain
47	chr1:150949200-150950400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr1:150949200-150950400	Flanking Active TSS	A549	lung
49	chr1:150949200-150950600	Flanking Active TSS	Hela-S3	cervix
50	chr1:150949200-150951600	Enhancers	Brain Cingulate Gyrus	brain

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