Variant report

Variant	rs17207622
Chromosome Location	chr6:31804173-31804174
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:122)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31801322-31807327	K562	blood:	n/a	n/a
2	GTF2F1	chr6:31803999-31804260	K562	blood:	n/a	n/a
3	POLR2A	chr6:31803746-31804291	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr6:31803963-31804628	GM18951	blood:	n/a	n/a
5	TAF7	chr6:31803544-31804371	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAX	chr6:31803910-31804360	K562	blood:	n/a	n/a
7	WRNIP1	chr6:31803982-31804337	GM12878	blood:	n/a	n/a
8	POLR2A	chr6:31804066-31804409	U87	brain:	n/a	n/a
9	POLR2A	chr6:31801892-31807499	GM12892	blood:	n/a	n/a
10	POLR2A	chr6:31804066-31804388	U87	brain:	n/a	n/a
11	MAX	chr6:31803880-31804435	A549	lung:	n/a	n/a
12	POLR2A	chr6:31801963-31810342	PANC-1	pancreas:	n/a	n/a
13	POLR2A	chr6:31803831-31804332	Raji	blood:	n/a	n/a
14	ELK1	chr6:31804019-31804274	K562	blood:	n/a	n/a
15	E2F6	chr6:31804045-31804235	K562	blood:	n/a	n/a
16	POLR2A	chr6:31803765-31804374	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr6:31804011-31804311	GM12878	blood:	n/a	n/a
18	POLR2A	chr6:31803759-31804325	GM12891	blood:	n/a	n/a
19	IRF1	chr6:31803770-31805820	K562	blood:	n/a	chr6:31804381-31804395
20	POLR2A	chr6:31803643-31807146	HL-60	blood:	n/a	n/a
21	NFIC	chr6:31803780-31804544	GM12878	blood:	n/a	n/a
22	CHD1	chr6:31802371-31805289	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr6:31803786-31804320	GM12878	blood:	n/a	n/a
24	POLR2A	chr6:31803582-31804542	GM12892	blood:	n/a	n/a
25	HEY1	chr6:31803545-31804696	K562	blood:	n/a	n/a
26	POLR2A	chr6:31803729-31805859	K562	blood:	n/a	n/a
27	TEAD4	chr6:31803538-31805859	K562	blood:	n/a	n/a
28	HEY1	chr6:31801932-31809366	HepG2	liver:	n/a	chr6:31802428-31802443
29	PAX5	chr6:31803950-31804286	GM12878	blood:	n/a	n/a
30	MXI1	chr6:31803736-31804306	K562	blood:	n/a	n/a
31	POLR2A	chr6:31803771-31804339	HepG2	liver:	n/a	n/a
32	MYC	chr6:31802073-31805549	K562	blood:	n/a	chr6:31802670-31802680
33	ZNF384	chr6:31801267-31804325	K562	blood:	n/a	n/a
34	MEF2A	chr6:31804151-31804603	GM12878	blood:	n/a	chr6:31804362-31804377 chr6:31804361-31804377
35	POLR2A	chr6:31802091-31809648	K562	blood:	n/a	n/a
36	POLR2A	chr6:31801829-31816167	SK-N-MC	brain:	n/a	n/a
37	MAX	chr6:31803993-31804302	GM12878	blood:	n/a	n/a
38	MAX	chr6:31801806-31804734	K562	blood:	n/a	chr6:31802670-31802680
39	MYC	chr6:31804057-31804236	MCF-7	breast:	n/a	n/a
40	POLR2A	chr6:31803755-31804344	MCF-7	breast:	n/a	n/a
41	SIN3AK20	chr6:31804119-31804430	PFSK-1	brain:	n/a	n/a
42	TBL1XR1	chr6:31804001-31805904	K562	blood:	n/a	n/a
43	POLR2A	chr6:31802046-31807267	MCF-7	breast:	n/a	n/a
44	POLR2A	chr6:31801886-31806082	GM12892	blood:	n/a	n/a
45	POLR2A	chr6:31804017-31804310	ProgFib	skin:	n/a	n/a
46	POLR2A	chr6:31802009-31806310	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr6:31804152-31804182	MCF-7	breast:	n/a	n/a
48	FOXM1	chr6:31804149-31805392	GM12878	blood:	n/a	n/a
49	POLR2A	chr6:31803772-31806451	GM12878	blood:	n/a	n/a
50	SIN3AK20	chr6:31803536-31805832	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31804172-31804222	NH-A	brain:	n/a
2	chr6:31804159-31804209	MCF-7	breast:	n/a
3	chr6:31804159-31804209	K562	blood:	n/a
4	chr6:31804172-31804222	MCF10A-Er-Src	breast:	n/a
5	chr6:31804159-31804209	MCF10A-Er-Src	breast:	n/a
6	chr6:31804159-31804209	HRCEpiC	kidney:	n/a
7	chr6:31804172-31804222	MCF-7	breast:	n/a
8	chr6:31804172-31804222	HCM	heart:	n/a
9	chr6:31804172-31804222	ProgFib	skin:	n/a
10	chr6:31804172-31804222	HRCEpiC	kidney:	n/a
11	chr6:31804172-31804222	A549	lung:	n/a
12	chr6:31804172-31804222	HCPEpiC	choroid plexus:	n/a
13	chr6:31804159-31804209	PrEC	prostate:	n/a
14	chr6:31804172-31804222	HRE	kidney:	n/a
15	chr6:31804159-31804209	BE2_C	brain:	n/a
16	chr6:31804172-31804222	IMR90	lung:	fetal
17	chr6:31804159-31804209	HNPCEpiC	eye:	n/a
18	chr6:31804159-31804209	NT2-D1	testis:	n/a
19	chr6:31804159-31804209	AoSMC	blood vessel:	n/a
20	chr6:31804159-31804209	HIPEpiC	eye:	n/a
21	chr6:31804159-31804209	HUVEC	blood vessel:	n/a
22	chr6:31804159-31804209	ECC-1	luminal epithelium:	n/a
23	chr6:31804172-31804222	PFSK-1	brain:	n/a
24	chr6:31804159-31804209	LNCaP	prostate:	n/a
25	chr6:31804159-31804209	H1-hESC	embryonic stem cell:	embryo
26	chr6:31804172-31804222	BE2_C	brain:	n/a
27	chr6:31804159-31804209	SK-N-SH_RA	brain:	n/a
28	chr6:31804172-31804222	HCF	heart:	n/a
29	chr6:31804172-31804222	AoSMC	blood vessel:	n/a
30	chr6:31804172-31804222	Jurkat	blood:	n/a
31	chr6:31804172-31804222	Caco-2	colon:	n/a
32	chr6:31804159-31804209	HL-60	blood:	n/a
33	chr6:31804159-31804209	GM12891	blood:	n/a
34	chr6:31804172-31804222	AG09319	gingival:	n/a
35	chr6:31804159-31804209	A549	lung:	n/a
36	chr6:31804172-31804222	AG04449	skin:	fetal
37	chr6:31804172-31804222	HAEpiC	amniotic membrane:	n/a
38	chr6:31804159-31804209	Caco-2	colon:	n/a
39	chr6:31804159-31804209	AG10803	skin:	n/a
40	chr6:31804159-31804209	ovcar-3	ovarian:	n/a
41	chr6:31804159-31804209	PANC-1	pancreas:	n/a
42	chr6:31804172-31804222	NT2-D1	testis:	n/a
43	chr6:31804159-31804209	HCPEpiC	choroid plexus:	n/a
44	chr6:31804159-31804209	HRE	kidney:	n/a
45	chr6:31804159-31804209	GM12878	blood:	n/a
46	chr6:31804172-31804222	HepG2	liver:	n/a
47	chr6:31804172-31804222	GM19239	blood:	n/a
48	chr6:31804159-31804209	SAEC	small airway:	n/a
49	chr6:31804159-31804209	NHBE	bronchial:	n/a
50	chr6:31804159-31804209	BJ	skin:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31760851..31764032-chr6:31800769..31804370,7	MCF-7	breast:
2	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
3	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
4	chr6:31702549..31706090-chr6:31802474..31805993,4	MCF-7	breast:
5	chr6:31509889..31512472-chr6:31802635..31805585,2	MCF-7	breast:
6	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
7	chr6:31801616..31806746-chr6:31865132..31870777,8	MCF-7	breast:
8	chr6:31508602..31511012-chr6:31803135..31806104,3	K562	blood:
9	chr6:31802844..31805158-chr6:31938598..31941453,3	K562	blood:
10	chr6:31803796..31805306-chr6:32094285..32096124,2	K562	blood:
11	chr6:31801272..31804221-chr6:31918478..31920926,2	K562	blood:
12	chr6:31656454..31658818-chr6:31801447..31804411,2	MCF-7	breast:
13	chr6:31798354..31804916-chr6:31860790..31871982,18	MCF-7	breast:
14	chr19:811579..813681-chr6:31802411..31804366,2	K562	blood:
15	chr6:31802366..31805115-chr6:31938170..31940148,2	K562	blood:
16	chr1:181056898..181058839-chr6:31802790..31804747,2	MCF-7	breast:
17	chr6:31696408..31700150-chr6:31800226..31805691,5	MCF-7	breast:
18	chr6:31630921..31635353-chr6:31802314..31807064,6	MCF-7	breast:
19	chr6:31735011..31745595-chr6:31798203..31806127,22	MCF-7	breast:
20	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
21	chr6:31800867..31807275-chr6:31862460..31868132,16	K562	blood:
22	chr6:31802757..31805057-chr6:31913533..31915744,2	MCF-7	breast:
23	chr6:31800669..31805219-chr6:31862460..31868046,11	K562	blood:
24	chr6:31802171..31804335-chr6:31837175..31839959,2	MCF-7	breast:
25	chr6:31588069..31590107-chr6:31801555..31804354,2	MCF-7	breast:
26	chr6:31802718..31804825-chr6:31935287..31937664,2	K562	blood:
27	chr6:31513842..31516738-chr6:31801353..31804200,3	K562	blood:
28	chr6:31801352..31804698-chr6:31868339..31871951,3	K562	blood:
29	chr6:31747450..31751295-chr6:31800640..31804723,4	MCF-7	breast:
30	chr6:31800194..31804653-chr6:31841439..31846611,7	MCF-7	breast:
31	chr6:31758502..31767561-chr6:31786193..31804196,52	MCF-7	breast:
32	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
33	chr6:31697326..31699677-chr6:31802341..31805046,2	MCF-7	breast:

No data

Variant related genes	Relation type
C6orf48	TF binding region
SNORD52	TF binding region
SNORD52	CpG island
C6orf48	CpG island
ENSG00000265236	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000213676	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000263414	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000162783	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11965654	0.96[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs13193280	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17207552	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2227955	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34416404	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713489	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4947332	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55704201	0.82[EUR][1000 genomes]
rs59324322	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS 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	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
9	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
10	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS 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 target site	162 gene(s)	inside rSNPs	diseases
13	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
14	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
16	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
18	nsv884461	chr6:31785453-31827045	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
19	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
20	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
21	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
22	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
23	nsv884463	chr6:31797422-31827045	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31801400-31805000	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr6:31801600-31805000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:31801800-31805000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:31802000-31804400	Active TSS	Esophagus	oesophagus
5	chr6:31802000-31804400	Active TSS	Ovary	ovary
6	chr6:31802000-31804600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
7	chr6:31802000-31804600	Active TSS	GM12878-XiMat	blood
8	chr6:31802000-31807000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:31802200-31804200	Active TSS	Hela-S3	cervix
10	chr6:31802200-31804200	Active TSS	HMEC	breast
11	chr6:31802200-31804600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:31802200-31804800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:31802200-31806400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:31802600-31804400	Active TSS	Gastric	stomach
15	chr6:31802600-31806400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
16	chr6:31802800-31804200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
17	chr6:31802800-31804600	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr6:31802800-31805000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
19	chr6:31802800-31806400	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
20	chr6:31802800-31807400	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
21	chr6:31803000-31804200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr6:31803000-31804600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr6:31803000-31805000	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr6:31803000-31807400	Transcr. at gene 5' and 3'	K562	blood
25	chr6:31803000-31817200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr6:31803200-31804200	Flanking Active TSS	Primary B cells from peripheral blood	blood
27	chr6:31803200-31804200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:31803200-31804200	Flanking Active TSS	Brain Angular Gyrus	brain
29	chr6:31803200-31804200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr6:31803200-31804200	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr6:31803200-31805400	Flanking Active TSS	Primary hematopoietic stem cells	blood
32	chr6:31803400-31804400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:31803400-31804800	Weak transcription	Spleen	Spleen
34	chr6:31803400-31805400	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
35	chr6:31803400-31806400	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
36	chr6:31803600-31804200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:31803600-31804200	Flanking Active TSS	Fetal Brain Male	brain
38	chr6:31803600-31804600	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr6:31803600-31804600	Flanking Active TSS	Colonic Mucosa	Colon
40	chr6:31803600-31804800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr6:31803600-31804800	Flanking Active TSS	Fetal Brain Female	brain
42	chr6:31803600-31804800	Flanking Active TSS	Fetal Heart	heart
43	chr6:31803600-31805000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr6:31803600-31805400	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
45	chr6:31803600-31805400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr6:31803600-31805400	Flanking Active TSS	Brain Germinal Matrix	brain
47	chr6:31803600-31806200	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr6:31803600-31807000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
49	chr6:31803800-31804200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:31803800-31804200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell

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