Variant report

Variant	rs7805256
Chromosome Location	chr7:127001014-127001015
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:126989599..126991125-chr7:126999110..127001691,2	K562	blood:
2	chr7:126999623..127001403-chr7:127005210..127006767,2	MCF-7	breast:
3	chr7:126999289..127001644-chr7:127001695..127003278,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF800-2	chr7:126999844-127004813	NONHSAT123138

Variant related genes	Relation type
ENSG00000224138	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10487480	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs10954149	0.84[ASN][1000 genomes]
rs11563346	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs11563460	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11563467	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11563624	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11563628	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11563629	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11563630	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs11563634	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs11563641	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11563648	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11563650	1.00[CHB][hapmap];0.97[ASN][1000 genomes]
rs11563652	0.97[ASN][1000 genomes]
rs12672573	0.84[ASN][1000 genomes]
rs12706779	0.85[AFR][1000 genomes]
rs12706780	1.00[ASN][1000 genomes]
rs12706783	0.84[ASN][1000 genomes]
rs12706784	0.84[ASN][1000 genomes]
rs12706785	0.84[ASN][1000 genomes]
rs13228039	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13233168	1.00[ASN][1000 genomes]
rs13246300	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1361937	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs1361938	0.95[YRI][hapmap]
rs1361939	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs1419395	1.00[YRI][hapmap]
rs1419396	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs1419398	0.84[ASN][1000 genomes]
rs1419399	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1419414	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17862368	0.84[ASN][1000 genomes]
rs17862369	0.84[ASN][1000 genomes]
rs17863291	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs17863295	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17863297	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17864195	0.97[ASN][1000 genomes]
rs17865345	0.90[ASN][1000 genomes]
rs17867824	0.97[ASN][1000 genomes]
rs17867840	1.00[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs17867842	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2027954	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2040500	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2188182	0.85[AFR][1000 genomes]
rs2269729	0.81[CHB][hapmap]
rs2402858	0.86[AFR][1000 genomes]
rs2402860	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs3944151	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4731350	0.95[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4731351	0.87[AFR][1000 genomes]
rs6467122	1.00[YRI][hapmap]
rs6957320	1.00[YRI][hapmap]
rs6959198	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs6972420	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71578227	0.97[ASN][1000 genomes]
rs7781891	1.00[ASN][1000 genomes]
rs7805194	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs916601	0.85[AFR][1000 genomes]
rs951808	1.00[YRI][hapmap];0.87[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017145	chr7:126995304-127015459	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126987800-127020600	Weak transcription	Spleen	Spleen
2	chr7:126988400-127001200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:126988400-127002200	Weak transcription	Fetal Heart	heart
4	chr7:126988400-127004400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr7:126988400-127006400	Weak transcription	Psoas Muscle	Psoas
6	chr7:126988400-127012600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:126988400-127013000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:126988400-127013000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr7:126988400-127013200	Weak transcription	NHEK	skin
10	chr7:126988400-127013400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:126988400-127014000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:126988400-127030200	Weak transcription	Fetal Intestine Small	intestine
13	chr7:126988400-127031400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:126988400-127031400	Weak transcription	Colonic Mucosa	Colon
15	chr7:126988400-127031400	Weak transcription	Pancreas	Pancrea
16	chr7:126988600-127007000	Weak transcription	A549	lung
17	chr7:126988600-127013400	Weak transcription	Colon Smooth Muscle	Colon
18	chr7:126988800-127005000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:126989000-127031000	Weak transcription	Fetal Brain Male	brain
20	chr7:126991600-127030400	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr7:126994000-127019800	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr7:126994600-127002200	Strong transcription	K562	blood
23	chr7:126995200-127007800	Weak transcription	Brain Anterior Caudate	brain
24	chr7:126995400-127022600	Strong transcription	Dnd41	blood
25	chr7:126995600-127027600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr7:126996200-127013000	Weak transcription	Ovary	ovary
27	chr7:126996600-127006400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr7:126996800-127010600	Strong transcription	Primary T cells fromperipheralblood	blood
29	chr7:126996800-127013400	Weak transcription	Fetal Kidney	kidney
30	chr7:126997000-127012800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr7:126997400-127006200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr7:126997400-127031200	Weak transcription	Brain Substantia Nigra	brain
33	chr7:126998200-127020600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr7:126998400-127002600	Strong transcription	Primary B cells from cord blood	blood
35	chr7:126998400-127005600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:126998600-127010000	Strong transcription	Primary hematopoietic stem cells	blood
37	chr7:126998600-127013800	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr7:126998800-127001600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:126998800-127002000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:126998800-127003400	Strong transcription	HMEC	breast
41	chr7:126998800-127005400	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr7:126999200-127006800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:126999200-127013400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr7:126999200-127018000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:126999200-127027200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr7:126999400-127003400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:126999400-127013000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr7:126999400-127031400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:126999600-127001400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:126999600-127001400	Strong transcription	HSMM	muscle

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