Variant report

Variant	rs113187885
Chromosome Location	chr17:59477413-59477414
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:66)
CpG islands
(count:0)
Chromatin interactive
region (count:112)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:66 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr17:59476657-59477458	PFSK-1	brain:	n/a	n/a
2	POLR2A	chr17:59468390-59479830	ProgFib	skin:	n/a	n/a
3	SIN3AK20	chr17:59476582-59477945	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr17:59476801-59478058	MCF-7	breast:	n/a	n/a
5	MAX	chr17:59475775-59478184	A549	lung:	n/a	chr17:59475824-59475831
6	SUZ12	chr17:59473583-59483306	NT2-D1	testis:	n/a	n/a
7	MYC	chr17:59477212-59477438	MCF-7	breast:	n/a	n/a
8	HDAC2	chr17:59475758-59477463	HepG2	liver:	n/a	chr17:59476354-59476363
9	MXI1	chr17:59473914-59480739	SK-N-SH	brain:	n/a	n/a
10	POLR2A	chr17:59476793-59477954	Gliobla	brain:	n/a	n/a
11	POLR2A	chr17:59474725-59477471	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr17:59477113-59477481	A549	lung:	n/a	n/a
13	MYC	chr17:59477004-59477420	A549	lung:	n/a	n/a
14	POLR2A	chr17:59476321-59478110	MCF-7	breast:	n/a	n/a
15	TAF1	chr17:59476215-59477556	ECC-1	luminal epithelium:	n/a	n/a
16	EP300	chr17:59476228-59478443	SK-N-SH	brain:	n/a	chr17:59476559-59476568 chr17:59476419-59476435 chr17:59476600-59476616 chr17:59477414-59477430 chr17:59476764-59476780 chr17:59476778-59476794 chr17:59476500-59476509
17	TCF12	chr17:59476171-59477518	ECC-1	luminal epithelium:	n/a	n/a
18	MAZ	chr17:59472821-59478277	IMR90	lung:	n/a	chr17:59474298-59474308 chr17:59475824-59475831 chr17:59474536-59474546 chr17:59474205-59474214
19	ZBTB7A	chr17:59476149-59477631	ECC-1	luminal epithelium:	n/a	chr17:59476804-59476813
20	MAZ	chr17:59476235-59477895	Hela-S3	cervix:	n/a	n/a
21	HDAC2	chr17:59474717-59482617	MCF-7	breast:	n/a	chr17:59476354-59476363 chr17:59480823-59480832
22	YY1	chr17:59476235-59477469	HepG2	liver:	n/a	chr17:59477137-59477146 chr17:59476557-59476571 chr17:59476439-59476453 chr17:59476847-59476858 chr17:59476554-59476568
23	POLR2A	chr17:59475965-59477555	HepG2	liver:	n/a	n/a
24	MYC	chr17:59477047-59477472	HepG2	liver:	n/a	n/a
25	TAF1	chr17:59476578-59477450	SK-N-SH	brain:	n/a	n/a
26	CREB1	chr17:59475839-59477503	HepG2	liver:	n/a	n/a
27	TEAD4	chr17:59474770-59479769	A549	lung:	n/a	n/a
28	POLR2A	chr17:59476461-59477476	HEK293	kidney:	n/a	n/a
29	MEF2A	chr17:59475654-59477601	SK-N-SH	brain:	n/a	n/a
30	POLR2A	chr17:59473262-59482475	IMR90	lung:	n/a	n/a
31	MAX	chr17:59475547-59478525	HepG2	liver:	n/a	chr17:59475824-59475831
32	SUZ12	chr17:59477100-59483936	H1-hESC	embryonic stem cell:	n/a	n/a
33	PBX3	chr17:59476742-59477495	SK-N-SH	brain:	n/a	n/a
34	MAX	chr17:59476961-59477475	ECC-1	luminal epithelium:	n/a	n/a
35	ZBTB7A	chr17:59477251-59477414	HepG2	liver:	n/a	n/a
36	POLR2A	chr17:59476347-59477680	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr17:59477039-59477474	U87	brain:	n/a	n/a
38	POLR2A	chr17:59477153-59477470	A549	lung:	n/a	n/a
39	MXI1	chr17:59473244-59478459	IMR90	lung:	n/a	n/a
40	HA-E2F1	chr17:59477275-59477917	Hela-S3	cervix:	n/a	n/a
41	MAX	chr17:59476605-59477917	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr17:59477039-59477417	U87	brain:	n/a	n/a
43	MAX	chr17:59475992-59477490	A549	lung:	n/a	n/a
44	CREB1	chr17:59476584-59477471	A549	lung:	n/a	n/a
45	RAD21	chr17:59474328-59477891	IMR90	lung:	n/a	chr17:59476606-59476616 chr17:59475048-59475062 chr17:59476563-59476576 chr17:59474744-59474754 chr17:59475436-59475445
46	TEAD4	chr17:59476236-59477647	SK-N-SH	brain:	n/a	n/a
47	RXRA	chr17:59476223-59477447	SK-N-SH	brain:	n/a	chr17:59477093-59477113
48	JUND	chr17:59477007-59477809	A549	lung:	n/a	n/a
49	GATA3	chr17:59476519-59477481	A549	lung:	n/a	n/a
50	REST	chr17:59476647-59477414	SK-N-SH	brain:	n/a	n/a

No data

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:56320231..56321842-chr17:59476539..59478120,2	MCF-7	breast:
2	chr17:59476329..59477978-chr5:98107765..98110191,2	MCF-7	breast:
3	chr17:59474707..59482954-chr20:45984179..45991970,21	MCF-7	breast:
4	chr17:59475645..59478788-chr7:5462326..5465715,3	MCF-7	breast:
5	chr17:57915289..57917492-chr17:59475690..59478863,6	MCF-7	breast:
6	chr10:101379177..101382119-chr17:59476299..59478201,2	MCF-7	breast:
7	chr15:72668330..72669227-chr17:59476887..59477547,2	MCF-7	breast:
8	chr17:59477279..59479183-chr17:59870460..59872520,2	MCF-7	breast:
9	chr17:58601262..58603520-chr17:59476586..59479561,3	MCF-7	breast:
10	chr17:59415713..59496229-chr20:49401322..49431802,760	MCF-7	breast:
11	chr17:57914760..57924876-chr17:59472133..59480361,28	MCF-7	breast:
12	chr17:57918266..57925909-chr17:59474699..59479743,11	MCF-7	breast:
13	chr17:59468937..59480240-chr20:49340039..49356868,49	MCF-7	breast:
14	chr17:59476086..59478200-chr5:14142004..14143977,2	MCF-7	breast:
15	chr17:57914749..57915447-chr17:59476989..59478273,3	MCF-7	breast:
16	chr17:59236660..59239548-chr17:59477347..59479433,2	MCF-7	breast:
17	chr12:1799825..1801584-chr17:59476233..59479039,2	MCF-7	breast:
18	chr17:59468469..59482635-chr20:45977748..45992950,51	MCF-7	breast:
19	chr17:59475321..59478062-chr9:127629865..127632518,2	MCF-7	breast:
20	chr16:30428172..30431085-chr17:59475920..59478019,2	MCF-7	breast:
21	chr17:59476334..59478740-chr7:100183272..100185013,2	MCF-7	breast:
22	chr17:59476055..59477880-chr20:47444208..47445878,2	MCF-7	breast:
23	chr1:226110432..226113669-chr17:59475384..59478027,3	MCF-7	breast:
24	chr17:59476401..59478732-chr17:59488339..59490282,10	MCF-7	breast:
25	chr17:59475983..59478702-chr20:60717939..60720042,2	MCF-7	breast:
26	chr17:59476586..59479504-chr20:45944218..45947716,4	MCF-7	breast:
27	chr17:56706858..56710627-chr17:59472052..59479583,11	MCF-7	breast:
28	chr16:89786416..89788600-chr17:59475587..59477647,2	MCF-7	breast:
29	chr17:59476542..59478104-chr2:208393472..208396208,2	MCF-7	breast:
30	chr17:59476078..59478218-chr3:195637161..195639509,2	MCF-7	breast:
31	chr17:59476268..59478751-chr17:73774327..73777038,2	MCF-7	breast:
32	chr17:59476060..59478361-chr3:73159086..73161459,2	MCF-7	breast:
33	chr17:59476138..59477780-chr3:64007387..64010093,2	MCF-7	breast:
34	chr1:113162339..113164666-chr17:59475031..59477488,2	MCF-7	breast:
35	chr1:173835625..173838583-chr17:59475360..59477954,2	MCF-7	breast:
36	chr17:56735328..56738474-chr17:59474554..59477882,3	MCF-7	breast:
37	chr17:59475836..59478140-chr4:140476860..140478447,2	MCF-7	breast:
38	chr1:149858261..149860142-chr17:59476311..59478808,2	MCF-7	breast:
39	chr17:59093635..59095394-chr17:59477039..59478884,2	MCF-7	breast:
40	chr17:59476370..59478594-chr2:24298301..24300623,2	MCF-7	breast:
41	chr17:59475358..59477997-chr20:52197460..52200356,2	MCF-7	breast:
42	chr1:114471153..114473640-chr17:59476771..59478545,2	MCF-7	breast:
43	chr17:58963859..58966065-chr17:59476840..59479002,2	MCF-7	breast:
44	chr17:59476717..59479924-chr6:6757897..6761293,3	MCF-7	breast:
45	chr17:57183794..57185492-chr17:59476524..59479346,2	MCF-7	breast:
46	chr15:78831864..78834406-chr17:59476584..59478636,2	MCF-7	breast:
47	chr12:122240766..122242888-chr17:59476165..59478324,2	MCF-7	breast:
48	chr17:59476079..59477930-chr2:25194673..25196791,2	MCF-7	breast:
49	chr17:59475732..59477627-chr6:26249790..26252547,2	MCF-7	breast:
50	chr17:59476933..59478370-chr20:49410741..49412054,5	MCF-7	breast:

No data

Variant related genes	Relation type
TBX2	TF binding region
ENSG00000267280	TF binding region
ENSG00000227896	Chromatin interaction
ENSG00000170836	Chromatin interaction
ENSG00000223247	Chromatin interaction
ENSG00000231437	Chromatin interaction
ENSG00000136950	Chromatin interaction
ENSG00000130703	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000132475	Chromatin interaction
ENSG00000050130	Chromatin interaction
ENSG00000153107	Chromatin interaction
ENSG00000110700	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000115137	Chromatin interaction
ENSG00000259349	Chromatin interaction
ENSG00000185278	Chromatin interaction
ENSG00000199787	Chromatin interaction
ENSG00000007341	Chromatin interaction
ENSG00000226308	Chromatin interaction
ENSG00000115128	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000200156	Chromatin interaction
ENSG00000145391	Chromatin interaction
ENSG00000254772	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000171792	Chromatin interaction
ENSG00000175895	Chromatin interaction
ENSG00000141376	Chromatin interaction
ENSG00000077454	Chromatin interaction
ENSG00000143811	Chromatin interaction
ENSG00000155287	Chromatin interaction
ENSG00000108395	Chromatin interaction
ENSG00000078246	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000155506	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000061938	Chromatin interaction
ENSG00000260339	Chromatin interaction
ENSG00000272953	Chromatin interaction
ENSG00000224165	Chromatin interaction
ENSG00000213614	Chromatin interaction
ENSG00000212694	Chromatin interaction
ENSG00000115677	Chromatin interaction
ENSG00000118260	Chromatin interaction
ENSG00000244687	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000170473	Chromatin interaction
ENSG00000197846	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000124126	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000038382	Chromatin interaction
ENSG00000132478	Chromatin interaction
ENSG00000167685	Chromatin interaction
ENSG00000260475	Chromatin interaction
ENSG00000163636	Chromatin interaction
ENSG00000062725	Chromatin interaction
ENSG00000171385	Chromatin interaction
ENSG00000177169	Chromatin interaction
ENSG00000184402	Chromatin interaction
ENSG00000172939	Chromatin interaction
ENSG00000225362	Chromatin interaction
ENSG00000158805	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000101182	Chromatin interaction
ENSG00000224738	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000126790	Chromatin interaction
ENSG00000083307	Chromatin interaction
ENSG00000187013	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000254024	Chromatin interaction
ENSG00000122692	Chromatin interaction
ENSG00000266163	Chromatin interaction
ENSG00000178149	Chromatin interaction
ENSG00000065357	Chromatin interaction
ENSG00000272717	Chromatin interaction
ENSG00000124243	Chromatin interaction
ENSG00000139718	Chromatin interaction
ENSG00000182095	Chromatin interaction
ENSG00000267882	Chromatin interaction
ENSG00000075399	Chromatin interaction
ENSG00000106009	Chromatin interaction
ENSG00000264063	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000263327	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000163349	Chromatin interaction
ENSG00000234741	Chromatin interaction
ENSG00000116489	Chromatin interaction
ENSG00000226155	Chromatin interaction
ENSG00000139725	Chromatin interaction
ENSG00000068650	Chromatin interaction
ENSG00000236352	Chromatin interaction
ENSG00000223725	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000197459	Chromatin interaction
ENSG00000204623	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000111206	Chromatin interaction
ENSG00000169762	Chromatin interaction
ENSG00000174136	Chromatin interaction
ENSG00000231119	Chromatin interaction
ENSG00000144401	Chromatin interaction
ENSG00000135269	Chromatin interaction
ENSG00000246763	Chromatin interaction
ENSG00000219626	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000103342	Chromatin interaction
ENSG00000256316	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000009307	Chromatin interaction
ENSG00000224532	Chromatin interaction
ENSG00000196420	Chromatin interaction
ENSG00000207605	Chromatin interaction
ENSG00000062650	Chromatin interaction
ENSG00000178057	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000264462	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000119397	Chromatin interaction
ENSG00000199032	Chromatin interaction
ENSG00000167964	Chromatin interaction
ENSG00000273451	Chromatin interaction
ENSG00000066379	Chromatin interaction
ENSG00000198162	Chromatin interaction
ENSG00000197451	Chromatin interaction
ENSG00000105185	Chromatin interaction
ENSG00000041357	Chromatin interaction
ENSG00000235527	Chromatin interaction
ENSG00000006831	Chromatin interaction
ENSG00000198900	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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	nsv1065939	chr17:59283350-59517730	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	331 gene(s)	inside rSNPs	diseases
2	nsv833505	chr17:59323466-59518007	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	326 gene(s)	inside rSNPs	diseases
3	nsv833506	chr17:59362377-59562984	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
4	nsv518130	chr17:59456589-59491281	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	265 gene(s)	inside rSNPs	diseases
5	esv1796927	chr17:59460119-59495319	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	270 gene(s)	inside rSNPs	diseases
6	nsv908663	chr17:59464069-59521310	Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	278 gene(s)	inside rSNPs	diseases
7	nsv908664	chr17:59465697-59491030	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	261 gene(s)	inside rSNPs	diseases
8	nsv908665	chr17:59470193-59494574	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	264 gene(s)	inside rSNPs	diseases
9	nsv908666	chr17:59470842-59489822	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	253 gene(s)	inside rSNPs	diseases
10	nsv908667	chr17:59471151-59491030	Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	256 gene(s)	inside rSNPs	diseases
11	nsv908668	chr17:59471151-59494574	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	263 gene(s)	inside rSNPs	diseases
12	nsv908669	chr17:59471372-59491030	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
13	nsv908670	chr17:59471372-59494574	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	262 gene(s)	inside rSNPs	diseases
14	esv3429164	chr17:59475870-59479468	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	156 gene(s)	inside rSNPs	diseases
15	nsv908671	chr17:59475888-59494574	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
16	nsv908672	chr17:59476062-59494574	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
17	esv3356501	chr17:59476195-59479343	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	156 gene(s)	inside rSNPs	diseases
18	esv3406346	chr17:59476220-59479068	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59473400-59479800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
2	chr17:59474200-59479000	Active TSS	Aorta	Aorta
3	chr17:59474200-59481000	Active TSS	NHDF-Ad	bronchial
4	chr17:59474400-59479800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
5	chr17:59475000-59479200	Active TSS	HSMM	muscle
6	chr17:59475000-59480400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
7	chr17:59475400-59478800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr17:59475400-59479600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
9	chr17:59475800-59478200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr17:59475800-59479400	Active TSS	Osteobl	bone
11	chr17:59476000-59478000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
12	chr17:59476000-59478200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr17:59476200-59478000	Active TSS	A549	lung
14	chr17:59476200-59478200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
15	chr17:59476200-59478200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
16	chr17:59476200-59478200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr17:59476200-59478200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr17:59476200-59478200	Bivalent/Poised TSS	Fetal Intestine Large	intestine
19	chr17:59476200-59478400	Active TSS	Hela-S3	cervix
20	chr17:59476200-59478600	Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr17:59476200-59478600	Active TSS	Muscle Satellite Cultured Cells	--
22	chr17:59476200-59478600	Active TSS	Fetal Kidney	kidney
23	chr17:59476200-59478800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr17:59476200-59479000	Active TSS	HSMMtube	muscle
25	chr17:59476200-59479600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr17:59476400-59477600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr17:59476400-59478000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr17:59476400-59478000	Active TSS	Fetal Lung	lung
29	chr17:59476400-59478000	Active TSS	NHLF	lung
30	chr17:59476400-59478200	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr17:59476400-59478200	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr17:59476400-59478200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
33	chr17:59476400-59478400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr17:59476400-59478600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr17:59476400-59478600	Bivalent/Poised TSS	Thymus	Thymus
36	chr17:59476400-59479000	Active TSS	Ovary	ovary
37	chr17:59476400-59479400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr17:59476600-59477800	Enhancers	Liver	Liver
39	chr17:59476600-59478000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
40	chr17:59476600-59478000	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
41	chr17:59476600-59478200	Bivalent/Poised TSS	Fetal Stomach	stomach
42	chr17:59476600-59478400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
43	chr17:59476600-59480600	Active TSS	Right Atrium	heart
44	chr17:59476800-59477600	Enhancers	Gastric	stomach
45	chr17:59476800-59477800	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr17:59476800-59477800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr17:59476800-59477800	Bivalent/Poised TSS	Esophagus	oesophagus
48	chr17:59476800-59478000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr17:59476800-59478000	Active TSS	Adipose Nuclei	Adipose
50	chr17:59476800-59478000	Bivalent/Poised TSS	HMEC	breast

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