Variant report

Variant	rs2072168
Chromosome Location	chr7:100861870-100861871
allele	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	ELF1	chr7:100860065-100861977	MCF-7	breast:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
2	MXI1	chr7:100859501-100862549	IMR90	lung:	n/a	chr7:100861332-100861347
3	SIN3AK20	chr7:100859882-100862120	MCF-7	breast:	n/a	n/a
4	POLR2A	chr7:100859817-100863220	HepG2	liver:	n/a	n/a
5	ELF1	chr7:100860292-100861898	GM12878	blood:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
6	CBX3	chr7:100859882-100862021	K562	blood:	n/a	n/a
7	SIN3AK20	chr7:100860513-100861879	A549	lung:	n/a	n/a
8	MYBL2	chr7:100861058-100862155	HepG2	liver:	n/a	n/a
9	MAX	chr7:100859842-100861976	K562	blood:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
10	TAF1	chr7:100860336-100861925	ECC-1	luminal epithelium:	n/a	n/a
11	ELF1	chr7:100860394-100861913	MCF-7	breast:	n/a	chr7:100861394-100861403 chr7:100860660-100860672
12	POLR2A	chr7:100860520-100861995	HepG2	liver:	n/a	n/a
13	TEAD4	chr7:100860544-100861992	K562	blood:	n/a	n/a
14	SIN3AK20	chr7:100860157-100861906	MCF-7	breast:	n/a	n/a
15	POLR2A	chr7:100860687-100861922	HepG2	liver:	n/a	n/a
16	MAX	chr7:100859833-100862032	MCF-7	breast:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
17	POLR2A	chr7:100860500-100862342	HepG2	liver:	n/a	n/a
18	GABPA	chr7:100860655-100861880	A549	lung:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861437-100861446
19	MXI1	chr7:100860207-100861887	HepG2	liver:	n/a	chr7:100861332-100861347
20	GABPA	chr7:100860198-100862232	MCF-7	breast:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861437-100861446
21	HDAC2	chr7:100861278-100861881	HepG2	liver:	n/a	n/a
22	YY1	chr7:100860130-100861937	SK-N-SH	brain:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
23	POLR2A	chr7:100859625-100861925	K562	blood:	n/a	n/a
24	ARID3A	chr7:100861267-100862060	HepG2	liver:	n/a	n/a
25	HEY1	chr7:100860525-100862029	HepG2	liver:	n/a	n/a
26	EGR1	chr7:100860261-100862053	HCT-116	colon:	n/a	chr7:100861288-100861297 chr7:100860332-100860342 chr7:100861517-100861530 chr7:100861372-100861381 chr7:100861436-100861445 chr7:100861395-100861404
27	NR2F2	chr7:100859676-100862425	K562	blood:	n/a	n/a
28	GABPA	chr7:100860349-100861955	K562	blood:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861437-100861446
29	POLR2A	chr7:100860511-100861903	HepG2	liver:	n/a	n/a
30	SP1	chr7:100860577-100861884	A549	lung:	n/a	chr7:100861522-100861536
31	YY1	chr7:100860346-100861962	HepG2	liver:	n/a	chr7:100861301-100861323 chr7:100861312-100861321
32	UBTF	chr7:100860069-100861872	K562	blood:	n/a	n/a
33	MAX	chr7:100859911-100861947	SK-N-SH	brain:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
34	NFIC	chr7:100860407-100861896	HepG2	liver:	n/a	n/a
35	GABPA	chr7:100860338-100862234	MCF-7	breast:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861437-100861446
36	TAF1	chr7:100861296-100861910	HepG2	liver:	n/a	n/a
37	MYBL2	chr7:100860512-100861924	HepG2	liver:	n/a	n/a
38	HCFC1	chr7:100859922-100862550	Hela-S3	cervix:	n/a	n/a
39	MAX	chr7:100859814-100861949	SK-N-SH	brain:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
40	MAX	chr7:100859831-100862089	A549	lung:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
41	GABPA	chr7:100860448-100861924	A549	lung:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861437-100861446
42	MAX	chr7:100860505-100861907	ECC-1	luminal epithelium:	n/a	chr7:100861338-100861347
43	TCF12	chr7:100860082-100861900	A549	lung:	n/a	n/a
44	TBP	chr7:100860681-100861892	HepG2	liver:	n/a	n/a
45	E2F6	chr7:100861559-100861882	K562	blood:	n/a	n/a
46	REST	chr7:100860009-100861998	H1-neurons	neurons:	n/a	chr7:100860575-100860585
47	MXI1	chr7:100859033-100862531	SK-N-SH	brain:	n/a	chr7:100861332-100861347
48	MAX	chr7:100859939-100861958	A549	lung:	n/a	chr7:100861338-100861347 chr7:100860333-100860343
49	MBD4	chr7:100860943-100861951	HepG2	liver:	n/a	n/a
50	NRF1	chr7:100860634-100861913	SK-N-SH	brain:	n/a	chr7:100861371-100861385 chr7:100861432-100861446 chr7:100861371-100861382 chr7:100861435-100861446 chr7:100861435-100861446 chr7:100861437-100861446

No.	Distal block	Cell Line	Cell type
1	chr7:100859700..100862927-chr7:100863052..100866687,4	MCF-7	breast:
2	chr7:100730924..100734717-chr7:100859526..100862672,3	MCF-7	breast:
3	chr7:100859374..100863045-chr7:100885733..100890781,8	K562	blood:
4	chr7:100859513..100863025-chr7:100885730..100890155,10	MCF-7	breast:
5	chr7:100858946..100862708-chr7:100892771..100897292,5	MCF-7	breast:
6	chr7:100858331..100862020-chr7:100880126..100882464,3	K562	blood:
7	chr7:100808076..100812812-chr7:100858488..100864832,8	MCF-7	breast:
8	chr7:100860572..100862632-chr7:100892717..100896862,3	K562	blood:
9	chr7:100796322..100799095-chr7:100860643..100862153,2	K562	blood:
10	chr7:100859409..100862433-chr7:100893851..100895703,4	K562	blood:
11	chr7:100858977..100861910-chr7:100881462..100883229,2	K562	blood:
12	chr7:100486477..100489401-chr7:100859928..100862607,2	MCF-7	breast:
13	chr7:100491458..100494589-chr7:100859109..100862606,4	MCF-7	breast:
14	chr7:100859877..100865511-chr7:100878168..100882490,7	MCF-7	breast:
15	chr7:100853413..100857189-chr7:100859048..100862216,5	K562	blood:
16	chr7:100796560..100798875-chr7:100861007..100862748,2	MCF-7	breast:
17	chr7:100858478..100862757-chr7:100884994..100890276,15	MCF-7	breast:
18	chr7:100853184..100857478-chr7:100859517..100863375,8	MCF-7	breast:
19	chr7:100859400..100864017-chr7:100886115..100890578,15	K562	blood:
20	chr7:100807333..100809689-chr7:100860017..100862230,2	K562	blood:
21	chr7:100850699..100858131-chr7:100858977..100863722,10	K562	blood:

Variant related genes	Relation type
PLOD3	TF binding region
ZNHIT1	TF binding region
ENSG00000169871	Chromatin interaction
ENSG00000106404	Chromatin interaction
ENSG00000214253	Chromatin interaction
ENSG00000176125	Chromatin interaction
ENSG00000106400	Chromatin interaction
ENSG00000106397	Chromatin interaction
ENSG00000128564	Chromatin interaction
ENSG00000106367	Chromatin interaction
ENSG00000087085	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10250685	0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.81[MKK][hapmap];0.94[ASN][1000 genomes]
rs1047319	1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1056678	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10953329	0.88[MEX][hapmap]
rs10953330	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11769624	0.81[ASW][hapmap];0.95[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.94[MEX][hapmap];0.94[MKK][hapmap];0.94[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11977597	0.83[CHB][hapmap];0.92[JPT][hapmap]
rs17319250	0.81[ASW][hapmap];0.95[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.94[MEX][hapmap];0.94[MKK][hapmap];0.94[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2074685	0.94[MEX][hapmap]
rs2302428	0.89[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.94[ASN][1000 genomes]
rs28361887	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35082269	0.98[ASN][1000 genomes]
rs35094522	0.94[MEX][hapmap];0.80[MKK][hapmap]
rs35550811	0.84[ASN][1000 genomes]
rs3757459	0.94[ASN][1000 genomes]
rs3757460	0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.81[MKK][hapmap];0.94[ASN][1000 genomes]
rs4729672	0.95[ASN][1000 genomes]
rs62482972	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831075	chr7:100692297-100917018	Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1030604	chr7:100717732-101223465	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	esv2422376	chr7:100743485-101016471	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS 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	63 gene(s)	inside rSNPs	diseases
5	nsv1018841	chr7:100760410-100868299	Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv534186	chr7:100773842-100898909	Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv607973	chr7:100782460-100873835	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
8	nsv888816	chr7:100792810-100862264	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv464651	chr7:100792810-100971604	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
10	nsv607974	chr7:100792810-100971604	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
11	nsv429788	chr7:100799565-101178565	Weak transcription Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers 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 miRNA target site	54 gene(s)	inside rSNPs	diseases
12	esv2752134	chr7:100800131-101141867	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
13	nsv607975	chr7:100804140-100873835	Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
14	nsv464652	chr7:100804140-100881640	Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv607976	chr7:100804140-100881640	Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv888817	chr7:100804140-100881640	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
17	nsv607977	chr7:100818846-100881640	Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
18	nsv831076	chr7:100828847-101011674	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv888818	chr7:100833153-100895480	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription 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 target site	29 gene(s)	inside rSNPs	diseases
20	nsv888819	chr7:100833153-100920007	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
21	esv2422326	chr7:100833449-101000131	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS 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 target site	37 gene(s)	inside rSNPs	diseases
22	nsv607978	chr7:100861213-100971604	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2072168	MYST3	trans	parietal	SCAN
rs2072168	TAC1	cis	parietal	SCAN

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100859200-100862200	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr7:100859400-100862600	Active TSS	HSMM	muscle
3	chr7:100859600-100862000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:100859600-100862400	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr7:100859600-100862400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:100859600-100862400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr7:100859600-100862600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:100859800-100862000	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr7:100859800-100862000	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr7:100859800-100862000	Active TSS	Right Atrium	heart
11	chr7:100859800-100862200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:100859800-100862200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:100859800-100862400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:100859800-100862400	Active TSS	H9 Cell Line	embryonic stem cell
15	chr7:100859800-100862600	Active TSS	HSMMtube	muscle
16	chr7:100860000-100862000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr7:100860000-100862000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr7:100860000-100862000	Active TSS	A549	lung
19	chr7:100860000-100862000	Active TSS	Hela-S3	cervix
20	chr7:100860000-100862000	Active TSS	Osteobl	bone
21	chr7:100860000-100862200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:100860000-100862200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:100860000-100862200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:100860000-100862200	Active TSS	Fetal Kidney	kidney
25	chr7:100860000-100862200	Active TSS	GM12878-XiMat	blood
26	chr7:100860000-100862200	Active TSS	HMEC	breast
27	chr7:100860000-100862200	Active TSS	NHDF-Ad	bronchial
28	chr7:100860000-100862400	Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr7:100860000-100862400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:100860000-100862400	Active TSS	Aorta	Aorta
31	chr7:100860000-100862400	Bivalent/Poised TSS	HepG2	liver
32	chr7:100860000-100862400	Active TSS	NHLF	lung
33	chr7:100860000-100862600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:100860200-100862000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:100860200-100862000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:100860200-100862000	Active TSS	Brain Angular Gyrus	brain
37	chr7:100860200-100862000	Active TSS	Brain Anterior Caudate	brain
38	chr7:100860200-100862000	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr7:100860200-100862000	Active TSS	Esophagus	oesophagus
40	chr7:100860200-100862000	Active TSS	Fetal Heart	heart
41	chr7:100860200-100862000	Active TSS	Gastric	stomach
42	chr7:100860200-100862000	Active TSS	Psoas Muscle	Psoas
43	chr7:100860200-100862000	Active TSS	Sigmoid Colon	Sigmoid Colon
44	chr7:100860200-100862000	Active TSS	Small Intestine	intestine
45	chr7:100860200-100862000	Active TSS	NHEK	skin
46	chr7:100860200-100862200	Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr7:100860200-100862400	Active TSS	H1 Cell Line	embryonic stem cell
48	chr7:100860200-100862400	Active TSS	HUES64 Cell Line	embryonic stem cell
49	chr7:100860200-100862400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr7:100860200-100863400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links