Variant report

Variant	rs3862907
Chromosome Location	chr1:92496655-92496656
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	E2F4	chr1:92496360-92496684	MCF10A-Er-Src	breast:	n/a	n/a
2	FOS	chr1:92496400-92496765	MCF10A-Er-Src	breast:	n/a	chr1:92496593-92496604 chr1:92496590-92496601 chr1:92496592-92496600 chr1:92496590-92496602
3	KAP1	chr1:92494860-92497177	HEK293	kidney:	n/a	n/a
4	POLR2A	chr1:92496296-92496747	HUVEC	blood vessel:	n/a	n/a
5	POLR2A	chr1:92495189-92496668	MCF10A-Er-Src	breast:	n/a	n/a
6	MYC	chr1:92495307-92496695	NB4	blood:	n/a	chr1:92495918-92495928
7	STAT3	chr1:92496420-92496737	MCF10A-Er-Src	breast:	n/a	n/a
8	POLR2A	chr1:92496201-92496943	HUVEC	blood vessel:	n/a	n/a
9	STAT3	chr1:92496506-92496786	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr1:92496299-92496797	MCF10A-Er-Src	breast:	n/a	chr1:92496593-92496604 chr1:92496590-92496601 chr1:92496592-92496600 chr1:92496590-92496602
11	STAT3	chr1:92496420-92496705	MCF10A-Er-Src	breast:	n/a	n/a
12	POLR2A	chr1:92496292-92496815	HCT-116	colon:	n/a	n/a
13	FOS	chr1:92496324-92496779	MCF10A-Er-Src	breast:	n/a	chr1:92496593-92496604 chr1:92496590-92496601 chr1:92496592-92496600 chr1:92496590-92496602
14	JUN	chr1:92496445-92497299	HUVEC	blood vessel:	n/a	chr1:92496865-92496873 chr1:92496593-92496604 chr1:92496592-92496600 chr1:92496590-92496602
15	MYC	chr1:92495986-92496729	MCF10A-Er-Src	breast:	n/a	n/a
16	KAP1	chr1:92495920-92497202	U2OS	brain:	n/a	n/a
17	MAX	chr1:92495319-92496769	NB4	blood:	n/a	chr1:92495918-92495928
18	FOS	chr1:92496389-92497352	HUVEC	blood vessel:	n/a	chr1:92496865-92496873 chr1:92496593-92496604 chr1:92496590-92496601 chr1:92496592-92496600 chr1:92496590-92496602
19	ZNF263	chr1:92494823-92496704	HEK293-T-REx	kidney:	n/a	chr1:92495986-92495995
20	MYC	chr1:92496124-92496778	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr1:92496352-92496730	HCT-116	colon:	n/a	n/a
22	FOS	chr1:92496446-92496746	MCF10A-Er-Src	breast:	n/a	chr1:92496593-92496604 chr1:92496590-92496601 chr1:92496592-92496600 chr1:92496590-92496602
23	SETDB1	chr1:92496252-92497166	U2OS	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
2	chr1:92494741..92496705-chr1:92764193..92766152,2	MCF-7	breast:
3	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:

Variant related genes	Relation type
EPHX4	TF binding region
ENSG00000189195	Chromatin interaction
ENSG00000122484	Chromatin interaction
ENSG00000174842	Chromatin interaction
ENSG00000172031	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs11466552	1.00[ASN][1000 genomes]
rs11466555	1.00[ASN][1000 genomes]
rs12032808	1.00[ASN][1000 genomes]
rs12071088	1.00[CHD][hapmap]
rs12739985	1.00[CHD][hapmap]
rs17131587	1.00[ASN][1000 genomes]
rs17131594	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131596	1.00[CHB][hapmap];1.00[MEX][hapmap]
rs17880479	1.00[MEX][hapmap]
rs17886020	1.00[ASN][1000 genomes]
rs2799519	1.00[ASN][1000 genomes]
rs2799520	1.00[ASN][1000 genomes]
rs3131816	1.00[CHB][hapmap]
rs3131824	1.00[CHB][hapmap]
rs4367824	1.00[ASN][1000 genomes]
rs475034	1.00[CHB][hapmap]
rs481384	1.00[CHB][hapmap]
rs495446	1.00[CHB][hapmap]
rs525834	1.00[CHB][hapmap]
rs533418	1.00[CHB][hapmap]
rs538054	1.00[CHB][hapmap]
rs541168	1.00[CHB][hapmap]
rs548100	1.00[CHB][hapmap]
rs553173	1.00[CHB][hapmap]
rs55813648	1.00[ASN][1000 genomes]
rs562119	1.00[CHB][hapmap]
rs564077	1.00[CHB][hapmap]
rs566576	1.00[CHB][hapmap]
rs57053265	1.00[ASN][1000 genomes]
rs58094327	1.00[ASN][1000 genomes]
rs58281825	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs59345962	1.00[ASN][1000 genomes]
rs60483196	1.00[ASN][1000 genomes]
rs60765274	1.00[ASN][1000 genomes]
rs61053596	1.00[ASN][1000 genomes]
rs6604065	1.00[ASN][1000 genomes]
rs6604066	1.00[ASN][1000 genomes]
rs6656473	1.00[ASN][1000 genomes]
rs6663157	1.00[ASN][1000 genomes]
rs6664544	1.00[CHB][hapmap]
rs6668529	1.00[CHB][hapmap]
rs66687439	1.00[ASN][1000 genomes]
rs6696071	1.00[CHB][hapmap]
rs6696315	1.00[ASN][1000 genomes]
rs6699466	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6700124	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[LWK][hapmap];0.91[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6703718	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs67510747	1.00[ASN][1000 genomes]
rs67577913	1.00[ASN][1000 genomes]
rs72716472	1.00[ASN][1000 genomes]
rs72716484	1.00[ASN][1000 genomes]
rs74101025	1.00[ASN][1000 genomes]
rs74101047	1.00[ASN][1000 genomes]
rs74101048	1.00[ASN][1000 genomes]
rs74101069	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74101079	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74101080	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74101081	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74101089	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs74101097	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7514679	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs7516778	1.00[ASN][1000 genomes]
rs7540938	1.00[ASN][1000 genomes]
rs7541252	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7544958	1.00[ASN][1000 genomes]
rs7545710	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs877277	1.00[ASN][1000 genomes]
rs883872	1.00[ASN][1000 genomes]
rs883873	1.00[ASN][1000 genomes]
rs9659484	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer 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	15 gene(s)	inside rSNPs	diseases
17	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
18	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv546820	chr1:92273644-92558583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
21	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv1002730	chr1:92302541-92565229	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
23	nsv830581	chr1:92317207-92511175	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
24	nsv871415	chr1:92340684-92641607	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
25	esv2750842	chr1:92356781-92579675	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
26	nsv871144	chr1:92380302-92641607	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	nsv1008863	chr1:92441031-92567045	Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
28	nsv535032	chr1:92441031-92567045	ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
29	nsv871606	chr1:92444125-92538104	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
30	nsv871508	chr1:92478130-92781579	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92494400-92497600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:92494800-92496800	Flanking Active TSS	HUVEC	blood vessel
3	chr1:92494800-92497000	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr1:92494800-92497000	Active TSS	Fetal Brain Female	brain
5	chr1:92494800-92497200	Active TSS	Brain Anterior Caudate	brain
6	chr1:92495200-92496800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr1:92495200-92496800	Active TSS	Brain Cingulate Gyrus	brain
8	chr1:92495200-92497400	Active TSS	Brain Angular Gyrus	brain
9	chr1:92496000-92497000	Enhancers	Hela-S3	cervix
10	chr1:92496000-92497200	Flanking Active TSS	Dnd41	blood
11	chr1:92496000-92497400	Enhancers	NHDF-Ad	bronchial
12	chr1:92496200-92496800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:92496200-92496800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:92496200-92496800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr1:92496200-92496800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:92496200-92496800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr1:92496200-92497000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr1:92496200-92497000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr1:92496200-92497000	Enhancers	Fetal Intestine Large	intestine
20	chr1:92496200-92497200	Enhancers	NHLF	lung
21	chr1:92496200-92497400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:92496200-92501000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:92496400-92496800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr1:92496400-92496800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
25	chr1:92496400-92496800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:92496400-92496800	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr1:92496400-92496800	Enhancers	Thymus	Thymus
28	chr1:92496400-92497000	Enhancers	Primary hematopoietic stem cells	blood
29	chr1:92496400-92497000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:92496400-92497000	Enhancers	NHEK	skin
31	chr1:92496400-92497200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:92496400-92497200	Enhancers	Fetal Intestine Small	intestine
33	chr1:92496400-92497400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:92496600-92496800	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr1:92496600-92496800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
36	chr1:92496600-92496800	Bivalent Enhancer	Primary T cells from cord blood	blood
37	chr1:92496600-92496800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:92496600-92496800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr1:92496600-92496800	Enhancers	HMEC	breast
40	chr1:92496600-92496800	Enhancers	NH-A	brain
41	chr1:92496600-92497000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
42	chr1:92496600-92497200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:92496600-92497200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr1:92496600-92497200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr1:92496600-92497200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:92496600-92497200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:92496600-92497600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:92496600-92499400	Weak transcription	Spleen	Spleen

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