Variant report

Variant	rs61843371
Chromosome Location	chr10:43362089-43362090
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	CTCF	chr10:43362060-43362210	NHEK	skin:	n/a	n/a
2	MAX	chr10:43361750-43362546	A549	lung:	n/a	n/a
3	RAD21	chr10:43361944-43362582	MCF-7	breast:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
4	MAX	chr10:43361499-43362154	MCF-7	breast:	n/a	n/a
5	GATA3	chr10:43361484-43362144	MCF-7	breast:	n/a	n/a
6	RAD21	chr10:43362027-43362593	ECC-1	luminal epithelium:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
7	HDAC2	chr10:43361452-43362542	MCF-7	breast:	n/a	n/a
8	IRF4	chr10:43361908-43362502	GM12878	blood:	n/a	n/a
9	ZNF263	chr10:43362044-43362517	HEK293-T-REx	kidney:	n/a	chr10:43362130-43362139
10	RAD21	chr10:43362067-43362608	H1-hESC	embryonic stem cell:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
11	CTCF	chr10:43361963-43362669	SK-N-SH	brain:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
12	TCF3	chr10:43361862-43362318	GM12878	blood:	n/a	n/a
13	CTCF	chr10:43362076-43362613	A549	lung:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
14	CTCF	chr10:43362083-43362485	K562	blood:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
15	HA-E2F1	chr10:43361413-43362458	MCF-7	breast:	n/a	n/a
16	RAD21	chr10:43362031-43362500	H1-hESC	embryonic stem cell:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
17	CTCF	chr10:43362015-43362660	HCT-116	colon:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
18	MYC	chr10:43361986-43362188	MCF-7	breast:	n/a	n/a
19	POLR2A	chr10:43361861-43362098	MCF-7	breast:	n/a	n/a
20	CTCF	chr10:43362060-43362210	BJ	skin:	n/a	n/a
21	CTCF	chr10:43361909-43362100	NHEK	skin:	n/a	n/a
22	MXI1	chr10:43361955-43362804	SK-N-SH	brain:	n/a	n/a
23	RAD21	chr10:43362009-43362686	H1-hESC	embryonic stem cell:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
24	RAD21	chr10:43361997-43362598	HCT-116	colon:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
25	CTCF	chr10:43361960-43362110	BE2_C	brain:	n/a	n/a
26	CTCF	chr10:43361951-43362668	A549	lung:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
27	CTCF	chr10:43361979-43362526	K562	blood:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
28	CTCF	chr10:43362075-43362509	A549	lung:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
29	RAD21	chr10:43361965-43362665	HCT-116	colon:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
30	CTCF	chr10:43361917-43362105	LNCaP	prostate:	n/a	n/a
31	CTCF	chr10:43362049-43362535	H1-hESC	embryonic stem cell:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
32	MAX	chr10:43361491-43362598	MCF-7	breast:	n/a	n/a
33	MAX	chr10:43362001-43362546	A549	lung:	n/a	n/a
34	POLR2A	chr10:43361871-43362157	MCF-7	breast:	n/a	n/a
35	SP1	chr10:43362075-43362386	GM12878	blood:	n/a	n/a
36	SMC3	chr10:43361779-43363127	SK-N-SH	brain:	n/a	chr10:43362285-43362299 chr10:43362262-43362270
37	FOSL2	chr10:43362064-43362518	HepG2	liver:	n/a	n/a
38	RAD21	chr10:43361902-43363340	SK-N-SH	brain:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398
39	CTCF	chr10:43362013-43362584	MCF-7	breast:	n/a	chr10:43362283-43362301 chr10:43362286-43362299 chr10:43362285-43362306 chr10:43362284-43362300
40	MAX	chr10:43362041-43362506	K562	blood:	n/a	n/a
41	RAD21	chr10:43362080-43362474	HepG2	liver:	n/a	chr10:43362284-43362303 chr10:43362285-43362299 chr10:43362385-43362398

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43362076-43362126	HPAEpiC	pulmonary alveolar:	n/a
2	chr10:43362076-43362126	HMEC	breast:	n/a
3	chr10:43362076-43362126	GM12878	blood:	n/a
4	chr10:43362076-43362126	MCF-7	breast:	n/a
5	chr10:43362076-43362126	Jurkat	blood:	n/a
6	chr10:43362076-43362126	SAEC	small airway:	n/a
7	chr10:43362076-43362126	GM12892	blood:	n/a
8	chr10:43362076-43362126	RPTEC	kidney:	n/a
9	chr10:43362076-43362126	HCF	heart:	n/a
10	chr10:43362076-43362126	GM12891	blood:	n/a
11	chr10:43362076-43362126	HL-60	blood:	n/a
12	chr10:43362076-43362126	HepG2	liver:	n/a
13	chr10:43362076-43362126	MCF10A-Er-Src	breast:	n/a
14	chr10:43362076-43362126	Caco-2	colon:	n/a
15	chr10:43362076-43362126	HEEpiC	esophagus:	n/a
16	chr10:43362076-43362126	T-47D	breast:	n/a
17	chr10:43362076-43362126	U87	brain:	n/a
18	chr10:43362076-43362126	SK-N-SH	brain:	n/a
19	chr10:43362076-43362126	A549	lung:	n/a
20	chr10:43362076-43362126	PrEC	prostate:	n/a
21	chr10:43362076-43362126	HRPEpiC	eye:	n/a
22	chr10:43362076-43362126	ovcar-3	ovarian:	n/a
23	chr10:43362076-43362126	BE2_C	brain:	n/a
24	chr10:43362076-43362126	AG10803	skin:	n/a
25	chr10:43362076-43362126	HUVEC	blood vessel:	n/a
26	chr10:43362076-43362126	AoSMC	blood vessel:	n/a
27	chr10:43362076-43362126	AG04449	skin:	fetal
28	chr10:43362076-43362126	Hela-S3	cervix:	n/a
29	chr10:43362076-43362126	AG04450	lung:	fetal
30	chr10:43362076-43362126	HNPCEpiC	eye:	n/a
31	chr10:43362076-43362126	HCM	heart:	n/a
32	chr10:43362076-43362126	Hepatocyte	liver:	n/a
33	chr10:43362076-43362126	PANC-1	pancreas:	n/a
34	chr10:43362076-43362126	SK-N-SH_RA	brain:	n/a
35	chr10:43362076-43362126	NT2-D1	testis:	n/a
36	chr10:43362076-43362126	HAEpiC	amniotic membrane:	n/a
37	chr10:43362076-43362126	CMK	blood:	n/a
38	chr10:43362076-43362126	NH-A	brain:	n/a
39	chr10:43362076-43362126	SKMC	muscle:	n/a
40	chr10:43362076-43362126	GM19239	blood:	n/a
41	chr10:43362076-43362126	NHBE	bronchial:	n/a
42	chr10:43362076-43362126	IMR90	lung:	fetal
43	chr10:43362076-43362126	AG09319	gingival:	n/a
44	chr10:43362076-43362126	HRE	kidney:	n/a
45	chr10:43362076-43362126	GM06990	blood:	n/a
46	chr10:43362076-43362126	H1-hESC	embryonic stem cell:	embryo
47	chr10:43362076-43362126	HRCEpiC	kidney:	n/a
48	chr10:43362076-43362126	NB4	blood:	n/a
49	chr10:43362076-43362126	HCT-116	colon:	n/a
50	chr10:43362076-43362126	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr10:43360364..43363685-chr10:43571830..43575400,3	MCF-7	breast:
2	chr10:43361867..43362389-chr10:43470791..43471531,2	K562	blood:
3	chr10:43359656..43362276-chr10:43538559..43540315,2	MCF-7	breast:
4	chr10:43361133..43364035-chr10:43632950..43635001,2	MCF-7	breast:
5	chr10:43361928..43362761-chr10:43600658..43601529,2	MCF-7	breast:
6	chr10:43355311..43356829-chr10:43360308..43362900,2	MCF-7	breast:
7	chr10:43361913..43362690-chr10:43470789..43471679,3	MCF-7	breast:
8	chr10:43360509..43362298-chr10:43627787..43629550,2	MCF-7	breast:
9	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
10	chr10:43361782..43362789-chr10:43574108..43574983,3	K562	blood:
11	chr10:43361871..43362799-chr10:43470867..43471733,6	MCF-7	breast:
12	chr10:43360554..43363791-chr10:43570974..43576100,9	MCF-7	breast:
13	chr10:43361854..43362671-chr10:43600633..43601533,4	K562	blood:

Variant related genes	Relation type
ENSG00000234944	TF binding region
ENSG00000234944	CpG island
ENSG00000273008	Chromatin interaction
ENSG00000169826	Chromatin interaction
ENSG00000165731	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1085783	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1091925	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1342143	0.83[EUR][1000 genomes]
rs1625947	0.83[EUR][1000 genomes]
rs17158193	0.87[EUR][1000 genomes]
rs17159047	0.87[EUR][1000 genomes]
rs17159071	0.87[EUR][1000 genomes]
rs17159198	0.89[EUR][1000 genomes]
rs17344904	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17344997	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17345889	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17429275	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17429415	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17430796	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1775069	0.83[EUR][1000 genomes]
rs1935644	0.83[EUR][1000 genomes]
rs2078397	0.89[EUR][1000 genomes]
rs2744082	0.83[EUR][1000 genomes]
rs2795505	0.80[EUR][1000 genomes]
rs2796563	0.83[EUR][1000 genomes]
rs2796565	0.83[EUR][1000 genomes]
rs41295810	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61736599	0.85[EUR][1000 genomes]
rs61843368	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61843372	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61843374	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61843382	0.94[AMR][1000 genomes]
rs61843955	0.83[AMR][1000 genomes]
rs61843956	0.83[AMR][1000 genomes]
rs61843958	0.83[AMR][1000 genomes]
rs61843959	0.83[AMR][1000 genomes]
rs61844765	0.83[AMR][1000 genomes]
rs61844768	0.83[AMR][1000 genomes]
rs61844771	0.83[AMR][1000 genomes]
rs61844772	0.83[AMR][1000 genomes]
rs61844774	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844775	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844813	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844814	0.87[EUR][1000 genomes]
rs61844815	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844816	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844817	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844821	0.87[EUR][1000 genomes]
rs61844822	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844827	0.87[EUR][1000 genomes]
rs61844828	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844829	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61844830	0.88[EUR][1000 genomes]
rs61844832	0.89[EUR][1000 genomes]
rs61844835	0.85[EUR][1000 genomes]
rs61844837	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61844848	0.89[EUR][1000 genomes]
rs61844849	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61844854	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61845960	0.81[EUR][1000 genomes]
rs61845963	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61845964	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7089165	0.85[EUR][1000 genomes]
rs7091439	0.89[EUR][1000 genomes]
rs788248	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs788250	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs788286	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs788294	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7904220	0.87[EUR][1000 genomes]
rs7908539	0.89[EUR][1000 genomes]
rs7915796	0.87[EUR][1000 genomes]
rs7923121	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550672	chr10:42753190-43441729	Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1042764	chr10:42846383-43511712	Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1050394	chr10:42890663-43604956	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	nsv540573	chr10:42890663-43604956	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv534548	chr10:42890664-43729688	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	esv2758216	chr10:42965131-43510191	Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
7	esv2759746	chr10:42965131-43510191	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
8	nsv1047838	chr10:43234590-43379219	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer 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 miRNA target site	18 gene(s)	inside rSNPs	diseases
9	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
10	nsv947892	chr10:43358233-43368929	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43361400-43362200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:43361400-43362600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:43361400-43362600	Bivalent/Poised TSS	Fetal Brain Female	brain
4	chr10:43361600-43362200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr10:43361600-43362200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr10:43361600-43362200	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:43361600-43362200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
8	chr10:43361600-43362200	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr10:43361600-43362200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:43361600-43362200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr10:43361600-43362200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr10:43361600-43362200	Bivalent Enhancer	Liver	Liver
13	chr10:43361600-43362200	Active TSS	Brain Anterior Caudate	brain
14	chr10:43361600-43362200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
15	chr10:43361600-43362200	Enhancers	Placenta Amnion	Placenta Amnion
16	chr10:43361600-43362200	Enhancers	Spleen	Spleen
17	chr10:43361600-43362200	Flanking Active TSS	HMEC	breast
18	chr10:43361600-43362200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
19	chr10:43361600-43362400	Enhancers	Primary B cells from cord blood	blood
20	chr10:43361600-43362400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
21	chr10:43361600-43362400	Active TSS	Right Ventricle	heart
22	chr10:43361600-43362600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
23	chr10:43361600-43362600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr10:43361600-43362600	Enhancers	Pancreas	Pancrea
25	chr10:43361600-43362600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
26	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
27	chr10:43361800-43362200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr10:43361800-43362200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
30	chr10:43361800-43362200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
31	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
32	chr10:43361800-43362200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:43361800-43362200	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
35	chr10:43361800-43362200	Flanking Active TSS	Primary hematopoietic stem cells	blood
36	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
37	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr10:43361800-43362200	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
39	chr10:43361800-43362200	Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
41	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
42	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
43	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
44	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
45	chr10:43361800-43362200	Bivalent Enhancer	Fetal Kidney	kidney
46	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
47	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
48	chr10:43361800-43362200	Bivalent Enhancer	Fetal Thymus	thymus
49	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
50	chr10:43361800-43362200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links