Variant report

Variant	rs7184263
Chromosome Location	chr16:30933064-30933065
allele	C/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	RFX5	chr16:30933002-30933162	HepG2	liver:	n/a	chr16:30933099-30933114
2	YY1	chr16:30932864-30934987	GM12892	blood:	n/a	chr16:30933963-30933971 chr16:30934069-30934083 chr16:30934055-30934074 chr16:30934368-30934387 chr16:30934548-30934556 chr16:30934244-30934252 chr16:30933960-30933970 chr16:30934371-30934379 chr16:30934057-30934079 chr16:30934803-30934812 chr16:30933960-30933982 chr16:30934373-30934381 chr16:30934370-30934380 chr16:30934058-30934066 chr16:30934057-30934067 chr16:30934060-30934068 chr16:30934543-30934562
3	CTCF	chr16:30933040-30933190	K562	blood:	n/a	chr16:30933085-30933095
4	CTCF	chr16:30932839-30933316	H1-hESC	embryonic stem cell:	n/a	chr16:30933085-30933095
5	MXI1	chr16:30932944-30933264	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr16:30932980-30933130	HCM	heart:	n/a	chr16:30933085-30933095
7	POLR2A	chr16:30932994-30934754	IMR90	lung:	n/a	n/a
8	MAX	chr16:30932857-30934906	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr16:30932977-30933194	A549	lung:	n/a	chr16:30933085-30933095
10	MXI1	chr16:30932916-30934862	HepG2	liver:	n/a	n/a
11	GABPA	chr16:30932930-30935065	MCF-7	breast:	n/a	chr16:30933932-30933946 chr16:30934803-30934812
12	CTCF	chr16:30933040-30933190	GM12871	blood:	n/a	chr16:30933085-30933095
13	CTCF	chr16:30933040-30933190	GM12875	blood:	n/a	chr16:30933085-30933095
14	RAD21	chr16:30932863-30933473	HepG2	liver:	n/a	chr16:30933084-30933094
15	POLR2A	chr16:30932820-30935110	PANC-1	pancreas:	n/a	n/a
16	RAD21	chr16:30932785-30933348	H1-hESC	embryonic stem cell:	n/a	chr16:30933084-30933094
17	CTCF	chr16:30933040-30933190	AoAF	blood vessel:	n/a	chr16:30933085-30933095
18	RAD21	chr16:30932925-30933324	A549	lung:	n/a	chr16:30933084-30933094
19	CTCF	chr16:30932980-30933130	HMF	breast:	n/a	chr16:30933085-30933095
20	CTCF	chr16:30932757-30933410	K562	blood:	n/a	chr16:30933085-30933095
21	CTCF	chr16:30933020-30933170	Caco-2	colon:	n/a	chr16:30933085-30933095
22	CTCF	chr16:30933000-30933150	HFF-Myc	foreskin:	n/a	chr16:30933085-30933095
23	MYC	chr16:30933021-30933186	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr16:30933000-30933150	GM12873	blood:	n/a	chr16:30933085-30933095
25	ZNF143	chr16:30932963-30933189	Hela-S3	cervix:	n/a	chr16:30933086-30933104
26	POLR2A	chr16:30932733-30935154	HepG2	liver:	n/a	n/a
27	CTCF	chr16:30933020-30933170	RPTEC	kidney:	n/a	chr16:30933085-30933095
28	YY1	chr16:30932965-30933413	HepG2	liver:	n/a	n/a
29	ELF1	chr16:30932843-30933284	HepG2	liver:	n/a	n/a
30	POLR2A	chr16:30932808-30935284	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr16:30933002-30933216	A549	lung:	n/a	chr16:30933085-30933095
32	CTCF	chr16:30932875-30933305	K562	blood:	n/a	chr16:30933085-30933095
33	CTCF	chr16:30932980-30933130	HVMF	connective:	n/a	chr16:30933085-30933095
34	CTCF	chr16:30932980-30933130	BE2_C	brain:	n/a	chr16:30933085-30933095
35	CTCF	chr16:30933020-30933170	HCPEpiC	choroid plexus:	n/a	chr16:30933085-30933095
36	POLR2A	chr16:30932910-30935253	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr16:30932904-30934842	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr16:30933000-30933150	HMF	breast:	n/a	chr16:30933085-30933095
39	CTCF	chr16:30932980-30933130	GM12869	blood:	n/a	chr16:30933085-30933095
40	HEY1	chr16:30932847-30934793	HepG2	liver:	n/a	n/a
41	CTCF	chr16:30933060-30933210	RPTEC	kidney:	n/a	chr16:30933085-30933095
42	POLR2A	chr16:30932734-30933484	GM12878	blood:	n/a	n/a
43	MAX	chr16:30933002-30933325	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr16:30932835-30934990	MCF-7	breast:	n/a	n/a
45	ZMIZ1	chr16:30932987-30934826	K562	blood:	n/a	n/a
46	YY1	chr16:30932806-30935038	HepG2	liver:	n/a	chr16:30933963-30933971 chr16:30934069-30934083 chr16:30934055-30934074 chr16:30934368-30934387 chr16:30934548-30934556 chr16:30934244-30934252 chr16:30933960-30933970 chr16:30934371-30934379 chr16:30934057-30934079 chr16:30934803-30934812 chr16:30933960-30933982 chr16:30934373-30934381 chr16:30934370-30934380 chr16:30934058-30934066 chr16:30934057-30934067 chr16:30934060-30934068 chr16:30934543-30934562
47	RAD21	chr16:30932751-30933540	MCF-7	breast:	n/a	chr16:30933084-30933094
48	CTCF	chr16:30932929-30933244	Medullo	brain:	n/a	chr16:30933085-30933095
49	RAD21	chr16:30932985-30933157	K562	blood:	n/a	chr16:30933084-30933094
50	POLR2A	chr16:30932776-30934737	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:30749500..30754511-chr16:30932304..30935822,6	MCF-7	breast:
2	chr16:30775945..30778308-chr16:30932961..30936468,4	MCF-7	breast:
3	chr16:30708299..30711208-chr16:30931702..30936734,5	MCF-7	breast:
4	chr16:30885123..30887354-chr16:30932881..30934600,2	K562	blood:
5	chr16:30902291..30910124-chr16:30929571..30937617,16	K562	blood:
6	chr16:30903642..30909138-chr16:30932304..30936727,12	MCF-7	breast:
7	chr16:30885239..30889762-chr16:30932057..30936596,5	K562	blood:
8	chr16:30795105..30800041-chr16:30931976..30937405,9	MCF-7	breast:
9	chr16:30666829..30670641-chr16:30932372..30935048,3	K562	blood:
10	chr16:30758359..30761183-chr16:30932981..30935164,3	MCF-7	breast:
11	chr16:30931053..30936697-chr16:30966530..30971104,6	MCF-7	breast:
12	chr16:30902664..30909579-chr16:30931454..30940613,20	MCF-7	breast:
13	chr16:30904870..30905744-chr16:30932719..30933286,2	MCF-7	breast:
14	chr16:30783772..30791593-chr16:30931071..30936822,9	MCF-7	breast:
15	chr16:30772454..30775297-chr16:30931524..30933572,3	MCF-7	breast:
16	chr16:30666829..30669508-chr16:30932265..30935039,3	K562	blood:
17	chr16:30771138..30775135-chr16:30932116..30935546,5	K562	blood:
18	chr16:30785189..30790485-chr16:30931540..30935208,7	K562	blood:
19	chr16:30673165..30675220-chr16:30931528..30934026,3	MCF-7	breast:
20	chr16:30785189..30790485-chr16:30931540..30936077,12	K562	blood:
21	chr16:30708050..30711529-chr16:30932244..30936391,8	K562	blood:
22	chr16:30932570..30935399-chr16:30951570..30953747,3	MCF-7	breast:
23	chr16:30855721..30856595-chr16:30932675..30933477,5	MCF-7	breast:
24	chr16:30714231..30716333-chr16:30932436..30935145,3	MCF-7	breast:
25	chr16:30660621..30663069-chr16:30932117..30934352,2	MCF-7	breast:
26	chr16:30771064..30772842-chr16:30931594..30934541,3	MCF-7	breast:
27	chr16:30717638..30720384-chr16:30932355..30934222,2	K562	blood:
28	chr16:30708909..30711747-chr16:30932178..30935236,6	MCF-7	breast:
29	chr16:30896338..30898892-chr16:30931663..30933817,2	MCF-7	breast:
30	chr16:30919055..30921667-chr16:30931962..30935622,4	K562	blood:
31	chr16:30932689..30934576-chr16:31084033..31085909,2	MCF-7	breast:
32	chr16:30885095..30888093-chr16:30931834..30934580,5	MCF-7	breast:
33	chr16:30932667..30934937-chr16:30952381..30954780,2	K562	blood:
34	chr16:30855781..30856646-chr16:30932589..30933506,4	K562	blood:
35	chr16:30904584..30910124-chr16:30931578..30937019,11	K562	blood:
36	chr16:30932533..30936330-chr16:30966882..30969248,5	K562	blood:
37	chr16:30707963..30711732-chr16:30932569..30936139,6	K562	blood:
38	chr16:30757630..30759751-chr16:30932681..30935536,3	K562	blood:
39	chr16:30931099..30935683-chr16:30951173..30955369,5	MCF-7	breast:
40	chr16:30932022..30936181-chr16:30958194..30961985,7	K562	blood:
41	chr16:30855497..30856657-chr16:30932633..30933761,9	MCF-7	breast:
42	chr16:30795368..30800075-chr16:30931111..30935900,11	MCF-7	breast:
43	chr16:30932533..30935734-chr16:30966751..30970803,5	K562	blood:
44	chr16:30825772..30826373-chr16:30932615..30933450,3	K562	blood:
45	chr16:30931619..30936181-chr16:30955998..30963201,14	K562	blood:
46	chr16:30883787..30888363-chr16:30930368..30933358,6	MCF-7	breast:
47	chr16:30784974..30791554-chr16:30930641..30936449,8	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL7C-2	chr16:30930640-30934590	ENSG00000260852.1

Variant related genes	Relation type
FBXL19	TF binding region
ENSG00000150281	Chromatin interaction
ENSG00000260899	Chromatin interaction
ENSG00000196118	Chromatin interaction
ENSG00000265991	Chromatin interaction
ENSG00000175938	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000156858	Chromatin interaction
ENSG00000103549	Chromatin interaction
ENSG00000260083	Chromatin interaction
ENSG00000156860	Chromatin interaction
ENSG00000262026	Chromatin interaction
ENSG00000099385	Chromatin interaction
ENSG00000102870	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000167395	Chromatin interaction
ENSG00000167394	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000261487	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000230447	Chromatin interaction
ENSG00000156873	Chromatin interaction
ENSG00000262721	Chromatin interaction
ENSG00000211591	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12102485	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13333418	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1870292	1.00[ASW][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2077633	1.00[MEX][hapmap]
rs28572417	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34212827	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4405566	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7203711	0.82[ASW][hapmap];1.00[MEX][hapmap];0.81[YRI][hapmap]
rs73526635	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73526645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8048593	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8050229	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8055067	0.84[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8061920	0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8062731	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9929927	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9940894	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh 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	437 gene(s)	inside rSNPs	diseases
3	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
4	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
5	esv1825223	chr16:30669091-30971810	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
6	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers 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	350 gene(s)	inside rSNPs	diseases
7	nsv905733	chr16:30796919-31004812	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer 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	112 gene(s)	inside rSNPs	diseases
8	nsv869652	chr16:30799471-30951038	Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers 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	70 gene(s)	inside rSNPs	diseases
9	nsv833189	chr16:30819708-30960795	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	79 gene(s)	inside rSNPs	diseases
10	nsv833190	chr16:30845051-31007863	Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
11	nsv833191	chr16:30864242-31048051	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	115 gene(s)	inside rSNPs	diseases
12	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
13	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
14	nsv905736	chr16:30900235-30995528	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
15	nsv905737	chr16:30900235-31014179	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
16	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
17	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription 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	253 gene(s)	inside rSNPs	diseases
18	nsv905738	chr16:30906274-30973926	Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30914000-30933200	Weak transcription	Ovary	ovary
2	chr16:30922800-30933200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:30932200-30936600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr16:30932400-30933200	Enhancers	Fetal Heart	heart
5	chr16:30932400-30934800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr16:30932600-30933200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr16:30932600-30933200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr16:30932600-30933400	Flanking Active TSS	Stomach Smooth Muscle	stomach
9	chr16:30932600-30933800	Flanking Active TSS	Dnd41	blood
10	chr16:30932600-30936000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr16:30932800-30933200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr16:30932800-30933200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr16:30932800-30933200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr16:30932800-30933200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
15	chr16:30932800-30933200	Enhancers	Spleen	Spleen
16	chr16:30932800-30933400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr16:30932800-30933400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr16:30932800-30933400	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr16:30932800-30933400	Flanking Active TSS	Brain Anterior Caudate	brain
20	chr16:30932800-30933400	Flanking Active TSS	Duodenum Mucosa	Duodenum
21	chr16:30932800-30933400	Flanking Active TSS	Placenta	Placenta
22	chr16:30932800-30933400	Flanking Active TSS	K562	blood
23	chr16:30932800-30933600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr16:30932800-30933600	Flanking Active TSS	Fetal Muscle Trunk	muscle
25	chr16:30932800-30933600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr16:30932800-30933600	Flanking Active TSS	Osteobl	bone
27	chr16:30932800-30933800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr16:30932800-30933800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr16:30932800-30933800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
30	chr16:30932800-30933800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr16:30932800-30933800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr16:30932800-30933800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr16:30932800-30933800	Flanking Active TSS	Hela-S3	cervix
34	chr16:30932800-30933800	Flanking Active TSS	NH-A	brain
35	chr16:30932800-30934600	Active TSS	NHDF-Ad	bronchial
36	chr16:30932800-30935000	Active TSS	Fetal Lung	lung
37	chr16:30932800-30935600	Active TSS	HUVEC	blood vessel
38	chr16:30932800-30935800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr16:30932800-30935800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr16:30932800-30935800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr16:30932800-30935800	Active TSS	Brain Hippocampus Middle	brain
42	chr16:30932800-30935800	Active TSS	Pancreas	Pancrea
43	chr16:30932800-30935800	Active TSS	Rectal Smooth Muscle	rectum
44	chr16:30932800-30935800	Active TSS	Thymus	Thymus
45	chr16:30932800-30936000	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr16:30932800-30936000	Active TSS	Brain Angular Gyrus	brain
47	chr16:30932800-30936000	Active TSS	Brain Cingulate Gyrus	brain
48	chr16:30932800-30936000	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr16:30932800-30936000	Active TSS	Fetal Brain Female	brain
50	chr16:30932800-30936000	Active TSS	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links