Variant report

Variant	rs7214884
Chromosome Location	chr17:59873238-59873239
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	JUND	chr17:59867807-59873404	MCF-7	breast:	n/a	chr17:59870743-59870752

No.	Distal block	Cell Line	Cell type
1	chr17:59873099..59874876-chr8:102504427..102506310,2	MCF-7	breast:
2	chr17:59834895..59837098-chr17:59871256..59875287,3	MCF-7	breast:
3	chr12:21193958..21195458-chr17:59872939..59874521,2	MCF-7	breast:

Variant related genes	Relation type
BRIP1	TF binding region
ENSG00000254024	Chromatin interaction
ENSG00000083307	Chromatin interaction

Extended variants
information (count: 109 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1015771	0.94[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10221278	0.87[CEU][hapmap]
rs10438771	0.87[CEU][hapmap]
rs10468558	0.87[CEU][hapmap]
rs10515206	0.87[CEU][hapmap]
rs10515207	0.87[CEU][hapmap]
rs10515211	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10853038	0.87[CEU][hapmap]
rs11079445	0.87[CEU][hapmap]
rs11650471	0.87[CEU][hapmap]
rs11653175	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11657480	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11658539	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11871753	0.88[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12451862	0.87[CEU][hapmap]
rs12453293	0.80[EUR][1000 genomes]
rs12453801	0.87[CEU][hapmap]
rs12453935	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12453966	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs12603617	0.87[CEU][hapmap]
rs12935923	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12937232	0.85[EUR][1000 genomes]
rs12948762	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12949659	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12950438	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1468577	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1541346	0.87[CEU][hapmap]
rs1978244	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1990337	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1990338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2024188	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2040608	0.87[CEU][hapmap]
rs2109252	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2109254	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2109255	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2159450	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2191247	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2191249	0.94[CEU][hapmap];0.84[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2378902	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2378905	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2378906	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28571892	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2890012	0.85[CEU][hapmap]
rs2890013	0.87[CEU][hapmap]
rs2890021	0.94[CEU][hapmap];0.84[CHB][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs36031690	0.83[EUR][1000 genomes]
rs4309463	0.85[EUR][1000 genomes]
rs4343344	0.85[EUR][1000 genomes]
rs4580256	0.80[EUR][1000 genomes]
rs4968444	0.86[CEU][hapmap]
rs4968447	0.87[CEU][hapmap];0.85[EUR][1000 genomes]
rs4968582	0.87[CEU][hapmap]
rs4988351	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57099937	0.80[EUR][1000 genomes]
rs57393813	0.80[EUR][1000 genomes]
rs62068837	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6504066	0.87[CEU][hapmap]
rs6504068	0.94[CEU][hapmap];0.83[CHB][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6504070	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6504071	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6504072	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs717961	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs717962	0.87[CEU][hapmap]
rs7207074	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs7207881	0.94[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7208704	0.93[CEU][hapmap];0.93[JPT][hapmap]
rs7212172	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7212423	0.87[CEU][hapmap];0.85[EUR][1000 genomes]
rs7213329	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7213470	0.85[EUR][1000 genomes]
rs7213587	0.87[CEU][hapmap];0.85[EUR][1000 genomes]
rs7215784	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7216011	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7216756	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7216824	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7217206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7217292	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7220688	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs7220719	0.87[CEU][hapmap];0.83[EUR][1000 genomes]
rs7222799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8074949	0.83[EUR][1000 genomes]
rs8075370	0.87[CEU][hapmap];0.85[EUR][1000 genomes]
rs8075397	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8077088	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8078977	0.94[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8182296	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs9303449	0.87[CEU][hapmap]
rs9889452	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9895987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9897121	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9897450	0.85[EUR][1000 genomes]
rs9897928	0.94[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9900559	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9902995	0.94[CEU][hapmap];0.84[CHB][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9904292	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9904294	0.85[EUR][1000 genomes]
rs9905870	0.82[EUR][1000 genomes]
rs9906313	0.94[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9907299	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs991378	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3378293	chr17:59744117-60124899	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	nsv908673	chr17:59767501-59926645	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases
3	nsv908674	chr17:59800827-59899790	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
4	nsv575841	chr17:59812748-59914681	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
5	nsv575842	chr17:59812748-59927307	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
6	nsv908675	chr17:59835864-59937286	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases
7	esv1794309	chr17:59861640-59907952	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region	32 gene(s)	inside rSNPs	diseases
8	esv1827960	chr17:59869069-59897455	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
9	nsv575843	chr17:59869081-59935723	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7214884	BRIP1	cis	Nerve Tibial	GTEx

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59816800-59887800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr17:59820400-59877200	Weak transcription	NH-A	brain
3	chr17:59825800-59898400	Weak transcription	Thymus	Thymus
4	chr17:59844000-59882600	Weak transcription	NHLF	lung
5	chr17:59844600-59882600	Weak transcription	HMEC	breast
6	chr17:59847600-59883400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr17:59847800-59876200	Weak transcription	Osteobl	bone
8	chr17:59848400-59873600	Weak transcription	K562	blood
9	chr17:59848600-59874000	Weak transcription	Hela-S3	cervix
10	chr17:59848600-59875600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr17:59848800-59882600	Weak transcription	NHEK	skin
12	chr17:59848800-59911200	Weak transcription	HUVEC	blood vessel
13	chr17:59849400-59887200	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr17:59849800-59887200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr17:59850000-59887000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr17:59850000-59887000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr17:59851200-59902600	Weak transcription	Fetal Stomach	stomach
18	chr17:59852600-59898000	Weak transcription	Fetal Intestine Small	intestine
19	chr17:59857000-59888600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr17:59860200-59883200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr17:59862000-59887200	Weak transcription	Fetal Kidney	kidney
22	chr17:59863600-59925000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr17:59863800-59876200	Weak transcription	GM12878-XiMat	blood
24	chr17:59865400-59873800	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr17:59866000-59880800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr17:59866000-59883200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr17:59866400-59883400	Weak transcription	Fetal Lung	lung
28	chr17:59867200-59881400	Strong transcription	Dnd41	blood
29	chr17:59867400-59875000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr17:59868000-59873600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr17:59868400-59888600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr17:59869200-59880600	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr17:59869200-59898200	Weak transcription	Fetal Muscle Leg	muscle
34	chr17:59869400-59876600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr17:59869400-59879000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr17:59869600-59887400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr17:59869800-59874400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr17:59870000-59882200	Weak transcription	NHDF-Ad	bronchial
39	chr17:59870200-59874000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr17:59870200-59875600	Weak transcription	HepG2	liver
41	chr17:59870400-59874200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr17:59870400-59933400	Weak transcription	Fetal Intestine Large	intestine
43	chr17:59870800-59874000	Strong transcription	Primary hematopoietic stem cells	blood
44	chr17:59871000-59878000	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr17:59871000-59880600	Weak transcription	Fetal Muscle Trunk	muscle
46	chr17:59871600-59875400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr17:59872000-59882200	Weak transcription	HSMM	muscle
48	chr17:59872200-59875000	Strong transcription	Fetal Thymus	thymus
49	chr17:59872200-59875400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr17:59872200-59876600	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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