Variant report

Variant	rs28365992
Chromosome Location	chr3:50340996-50340997
allele	A/C/G/T
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	POLR2A	chr3:50340246-50341385	K562	blood:	n/a	n/a
2	IRF1	chr3:50340777-50341289	K562	blood:	n/a	chr3:50341068-50341082 chr3:50341148-50341162
3	TBL1XR1	chr3:50340917-50341190	K562	blood:	n/a	n/a
4	POLR2A	chr3:50340726-50341355	HCT-116	colon:	n/a	n/a
5	CTCF	chr3:50340175-50341006	SK-N-SH	brain:	n/a	chr3:50340534-50340542 chr3:50340580-50340598 chr3:50340581-50340597
6	HEY1	chr3:50340723-50341092	K562	blood:	n/a	n/a
7	MAZ	chr3:50340389-50341232	HepG2	liver:	n/a	chr3:50341173-50341183
8	POLR2A	chr3:50340678-50341153	K562	blood:	n/a	n/a
9	POLR2A	chr3:50339436-50341410	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr3:50340195-50341136	HUVEC	blood vessel:	n/a	n/a
11	POLR2A	chr3:50340505-50341433	HCT-116	colon:	n/a	n/a
12	POLR2A	chr3:50340733-50341304	ECC-1	luminal epithelium:	n/a	n/a
13	MAX	chr3:50339747-50341427	HepG2	liver:	n/a	chr3:50341173-50341183
14	TAF1	chr3:50340235-50341359	HepG2	liver:	n/a	n/a
15	RFX5	chr3:50340876-50341274	Hela-S3	cervix:	n/a	n/a
16	SP1	chr3:50340275-50341339	HepG2	liver:	n/a	chr3:50341068-50341080 chr3:50341149-50341158 chr3:50341148-50341160 chr3:50341229-50341243 chr3:50341068-50341080 chr3:50341148-50341160 chr3:50341148-50341159 chr3:50341172-50341184 chr3:50341058-50341067 chr3:50341150-50341159 chr3:50341070-50341079 chr3:50341149-50341159 chr3:50341172-50341184 chr3:50341173-50341183 chr3:50341172-50341183 chr3:50340474-50340488 chr3:50341149-50341159 chr3:50341145-50341159
17	POLR2A	chr3:50340232-50341393	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr3:50340171-50341206	HepG2	liver:	n/a	n/a
19	POLR2A	chr3:50340698-50341134	Hela-S3	cervix:	n/a	n/a
20	TAL1	chr3:50340791-50341123	K562	blood:	n/a	n/a
21	POLR2A	chr3:50340778-50341347	K562	blood:	n/a	n/a
22	TBP	chr3:50340490-50341252	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAX	chr3:50340430-50341381	Hela-S3	cervix:	n/a	chr3:50341173-50341183
24	YY1	chr3:50340132-50341423	HepG2	liver:	n/a	n/a
25	MYC	chr3:50340259-50341168	HepG2	liver:	n/a	n/a
26	MBD4	chr3:50340137-50341188	HepG2	liver:	n/a	n/a
27	CHD2	chr3:50340382-50341265	HepG2	liver:	n/a	n/a
28	MAX	chr3:50339864-50341269	HepG2	liver:	n/a	chr3:50341173-50341183
29	REST	chr3:50340740-50341051	HepG2	liver:	n/a	chr3:50340888-50340908 chr3:50340888-50340908 chr3:50340891-50340904 chr3:50340833-50340842
30	POLR2A	chr3:50340540-50341336	H1-hESC	embryonic stem cell:	n/a	n/a
31	BHLHE40	chr3:50340923-50341226	K562	blood:	n/a	n/a
32	CEBPD	chr3:50340150-50341408	HepG2	liver:	n/a	n/a
33	POLR2A	chr3:50339443-50341454	HepG2	liver:	n/a	n/a
34	EP300	chr3:50340059-50341146	HepG2	liver:	n/a	n/a
35	POLR2A	chr3:50340163-50341346	HepG2	liver:	n/a	n/a
36	ELK1	chr3:50340833-50341211	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr3:50340365-50341390	K562	blood:	n/a	n/a
38	MAZ	chr3:50340392-50341352	K562	blood:	n/a	chr3:50341173-50341183
39	POLR2A	chr3:50340655-50341343	Hela-S3	cervix:	n/a	n/a
40	TAF1	chr3:50340795-50341107	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr3:50340785-50341202	K562	blood:	n/a	n/a
42	NFIC	chr3:50340154-50341088	HepG2	liver:	n/a	n/a
43	RCOR1	chr3:50340594-50341260	K562	blood:	n/a	n/a
44	POLR2A	chr3:50340830-50341030	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr3:50340746-50341137	Hela-S3	cervix:	n/a	n/a
46	GTF2F1	chr3:50340872-50341242	K562	blood:	n/a	n/a
47	TBP	chr3:50340581-50341345	K562	blood:	n/a	n/a
48	CHD2	chr3:50340526-50341345	Hela-S3	cervix:	n/a	n/a
49	ARID3A	chr3:50340342-50341187	HepG2	liver:	n/a	n/a
50	MAX	chr3:50340953-50341489	K562	blood:	n/a	chr3:50341173-50341183

No.	Distal block	Cell Line	Cell type
1	chr3:50339705..50341283-chr3:50377540..50380265,2	K562	blood:
2	chr3:50327926..50342388-chr3:50350886..50359960,36	MCF-7	breast:
3	chr3:50324564..50342616-chr3:50350801..50362499,49	MCF-7	breast:
4	chr18:74843234..74844124-chr3:50340676..50341490,2	Hela-S3	cervix:
5	chr3:50334885..50342502-chr3:50352987..50366859,26	K562	blood:
6	chr3:50340483..50341210-chrX:117480073..117480951,2	Hela-S3	cervix:
7	chr12:6309543..6310399-chr3:50340422..50341257,2	Hela-S3	cervix:
8	chr3:50340330..50341202-chr9:116037757..116038408,2	Hela-S3	cervix:
9	chr3:50334334..50341950-chr3:50357130..50360296,11	K562	blood:

Variant related genes	Relation type
HYAL3	TF binding region
NAT6	TF binding region
ENSG00000131725	Chromatin interaction
ENSG00000068028	Chromatin interaction
ENSG00000010278	Chromatin interaction
ENSG00000136875	Chromatin interaction
ENSG00000197971	Chromatin interaction
ENSG00000235058	Chromatin interaction
ENSG00000114383	Chromatin interaction
ENSG00000068001	Chromatin interaction
ENSG00000176386	Chromatin interaction
ENSG00000004838	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10510755	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[GIH][hapmap];0.94[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12629572	1.00[CEU][hapmap];0.95[GIH][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes]
rs12635953	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1989839	1.00[CEU][hapmap];0.95[GIH][hapmap];0.94[TSI][hapmap];0.81[EUR][1000 genomes]
rs2071802	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2071803	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.94[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2073498	1.00[ASW][hapmap];0.93[CEU][hapmap];0.82[CHB][hapmap];0.90[GIH][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2073499	0.93[CEU][hapmap]
rs2097247	0.82[AMR][1000 genomes]
rs2233474	0.93[CEU][hapmap]
rs2236939	0.86[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs2236950	1.00[ASW][hapmap];1.00[LWK][hapmap];0.89[MKK][hapmap]
rs2236967	1.00[ASW][hapmap]
rs2236968	1.00[ASW][hapmap]
rs2236988	1.00[ASW][hapmap]
rs2239801	1.00[CEU][hapmap];0.82[CHB][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2282756	1.00[ASW][hapmap]
rs2301639	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[GIH][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2526392	0.90[GIH][hapmap]
rs2526394	0.90[GIH][hapmap]
rs2526395	0.90[GIH][hapmap]
rs2526396	0.90[GIH][hapmap]
rs2624837	0.90[GIH][hapmap]
rs2624842	0.90[GIH][hapmap]
rs3755832	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3806708	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs41291724	0.85[AMR][1000 genomes]
rs4141060	0.93[CEU][hapmap]
rs45536634	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57319506	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57462170	0.86[EUR][1000 genomes]
rs57838764	0.82[EUR][1000 genomes]
rs58051625	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60247651	0.87[EUR][1000 genomes]
rs6776145	1.00[CEU][hapmap];0.95[GIH][hapmap];0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs762898	1.00[ASW][hapmap]
rs7642692	0.94[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
3	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
5	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
6	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
7	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
8	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
9	esv2757870	chr3:50198478-50371377	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
10	esv2759148	chr3:50198478-50371377	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
11	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
12	nsv590254	chr3:50243510-50388607	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
13	nsv460531	chr3:50247824-50436827	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
14	nsv590255	chr3:50247824-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
15	nsv876772	chr3:50255305-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
16	nsv590257	chr3:50302830-50393640	Genic enhancers Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
17	nsv590256	chr3:50302830-50420554	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
18	nsv876774	chr3:50302830-50436827	Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
19	nsv876773	chr3:50302830-50480131	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
20	nsv834693	chr3:50302830-50507964	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
21	nsv876775	chr3:50324672-50504896	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs28365992	SLC25A20	cis	cerebellum	SCAN
rs28365992	NEK4	cis	parietal	SCAN
rs28365992	ARIH2	cis	cerebellum	SCAN
rs28365992	TRAIP	cis	parietal	SCAN

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50337800-50353800	Weak transcription	HSMMtube	muscle
2	chr3:50338000-50341600	Enhancers	Fetal Muscle Trunk	muscle
3	chr3:50338000-50342200	Weak transcription	NH-A	brain
4	chr3:50338000-50343600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr3:50338000-50352400	Weak transcription	Fetal Kidney	kidney
6	chr3:50338200-50342000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr3:50338200-50343000	Weak transcription	Fetal Thymus	thymus
8	chr3:50338200-50344400	Weak transcription	Brain Germinal Matrix	brain
9	chr3:50338200-50352800	Weak transcription	Colon Smooth Muscle	Colon
10	chr3:50338200-50353800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr3:50338200-50353800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr3:50338200-50353800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr3:50338200-50356000	Weak transcription	Primary T cells from cord blood	blood
14	chr3:50338400-50341400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:50338400-50352800	Weak transcription	Brain Anterior Caudate	brain
16	chr3:50338600-50341000	Weak transcription	Fetal Brain Female	brain
17	chr3:50338600-50342000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr3:50338600-50355600	Weak transcription	Fetal Brain Male	brain
19	chr3:50338600-50355800	Weak transcription	Brain Angular Gyrus	brain
20	chr3:50338800-50352600	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr3:50338800-50353800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr3:50338800-50354000	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr3:50339200-50353000	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr3:50339400-50341400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:50339400-50341400	Flanking Active TSS	Hela-S3	cervix
26	chr3:50339400-50341800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr3:50339600-50341200	Genic enhancers	Fetal Stomach	stomach
28	chr3:50339600-50341400	Enhancers	Fetal Intestine Large	intestine
29	chr3:50339600-50341400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr3:50339800-50341000	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr3:50339800-50341200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr3:50339800-50341400	Enhancers	Ovary	ovary
33	chr3:50339800-50341600	Enhancers	Fetal Muscle Leg	muscle
34	chr3:50340000-50341000	Flanking Active TSS	Lung	lung
35	chr3:50340000-50341000	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr3:50340000-50341400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:50340200-50341000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:50340200-50341000	Active TSS	Liver	Liver
39	chr3:50340200-50341000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:50340200-50341000	Enhancers	Fetal Lung	lung
41	chr3:50340200-50341000	Active TSS	Rectal Smooth Muscle	rectum
42	chr3:50340200-50341000	Flanking Active TSS	Right Atrium	heart
43	chr3:50340200-50341000	Flanking Active TSS	Stomach Mucosa	stomach
44	chr3:50340200-50341000	Bivalent/Poised TSS	HepG2	liver
45	chr3:50340200-50341200	Enhancers	A549	lung
46	chr3:50340200-50341400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr3:50340200-50341400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr3:50340200-50341400	Enhancers	Fetal Heart	heart
49	chr3:50340200-50341600	Enhancers	Placenta	Placenta
50	chr3:50340400-50341000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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