Variant report

Variant	rs17883557
Chromosome Location	chr7:100494949-100494950
allele	A/C
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	CTCF	chr7:100494860-100495010	HRE	kidney:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
2	ETS1	chr7:100494102-100495052	K562	blood:	n/a	n/a
3	RAD21	chr7:100494791-100495006	K562	blood:	n/a	chr7:100494904-100494918 chr7:100494903-100494922
4	CTCF	chr7:100494681-100495040	ProgFib	skin:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
5	CTCF	chr7:100494820-100494970	AG04449	skin:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
6	CTCF	chr7:100494494-100495321	A549	lung:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
7	TBP	chr7:100494762-100495659	K562	blood:	n/a	n/a
8	NR2F2	chr7:100494819-100496082	K562	blood:	n/a	n/a
9	CTCF	chr7:100494840-100494990	AG04450	lung:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
10	CTCF	chr7:100494820-100494970	WERI-Rb-1	eye:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
11	REST	chr7:100494765-100495136	U87	brain:	n/a	n/a
12	CTCF	chr7:100494695-100495332	HCT-116	colon:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
13	CTCF	chr7:100494778-100495061	LNCaP	prostate:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
14	CTCF	chr7:100494656-100495114	GM19238	blood:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
15	RAD21	chr7:100494792-100494998	GM12878	blood:	n/a	chr7:100494904-100494918 chr7:100494903-100494922
16	RAD21	chr7:100494701-100495314	A549	lung:	n/a	chr7:100494904-100494918 chr7:100494903-100494922 chr7:100495270-100495284
17	JUN	chr7:100493191-100496118	K562	blood:	n/a	chr7:100494328-100494341 chr7:100493521-100493530
18	MYC	chr7:100494870-100494954	GM12878	blood:	n/a	n/a
19	FOXA1	chr7:100494833-100494992	T-47D	breast:	n/a	n/a
20	CTCF	chr7:100494860-100495010	HEEpiC	esophagus:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
21	CTCF	chr7:100494820-100494970	AG04450	lung:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
22	YY1	chr7:100494761-100495040	HCT-116	colon:	n/a	n/a
23	POLR2A	chr7:100494686-100495193	K562	blood:	n/a	n/a
24	RAD21	chr7:100494681-100495225	ECC-1	luminal epithelium:	n/a	chr7:100494904-100494918 chr7:100494903-100494922
25	CTCF	chr7:100494840-100494990	BJ	skin:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
26	CTCF	chr7:100494880-100495030	A549	lung:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
27	CTCF	chr7:100493591-100495920	SK-N-SH	brain:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494142-100494151 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
28	CTCF	chr7:100494642-100495200	H1-hESC	embryonic stem cell:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
29	CTCF	chr7:100494806-100495011	ECC-1	luminal epithelium:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
30	EBF1	chr7:100494816-100495071	GM12878	blood:	n/a	n/a
31	CTCF	chr7:100494716-100495048	K562	blood:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
32	CTCF	chr7:100494860-100495010	HRPEpiC	eye:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
33	MAX	chr7:100494896-100495178	NB4	blood:	n/a	n/a
34	CTCF	chr7:100494860-100495010	AG10803	skin:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
35	RUNX3	chr7:100494791-100494992	GM12878	blood:	n/a	n/a
36	CTCF	chr7:100494840-100494990	GM12864	blood:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
37	CTCF	chr7:100494673-100495323	MCF-7	breast:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
38	SMC3	chr7:100494812-100495071	HepG2	liver:	n/a	chr7:100494908-100494918 chr7:100494904-100494918
39	CTCF	chr7:100494742-100495044	NHEK	skin:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
40	MYC	chr7:100493631-100495749	K562	blood:	n/a	chr7:100493756-100493765 chr7:100494831-100494840 chr7:100493755-100493766
41	CTCF	chr7:100494820-100494970	GM12801	blood:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
42	CTCF	chr7:100494860-100495010	HPAF	blood vessel:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
43	CTCF	chr7:100494840-100494990	AG09319	gingival:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
44	RAD21	chr7:100494698-100495198	H1-hESC	embryonic stem cell:	n/a	chr7:100494904-100494918 chr7:100494903-100494922
45	YY1	chr7:100494766-100495057	GM12878	blood:	n/a	n/a
46	CTCF	chr7:100494825-100495005	HepG2	liver:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
47	CBX3	chr7:100494678-100495986	K562	blood:	n/a	n/a
48	CTCF	chr7:100494860-100495010	Hela-S3	cervix:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925
49	GTF2F1	chr7:100494829-100494964	K562	blood:	n/a	n/a
50	CTCF	chr7:100494759-100495035	Lung_OC	lung:	n/a	chr7:100494903-100494919 chr7:100494902-100494920 chr7:100494902-100494915 chr7:100494905-100494918 chr7:100494905-100494918 chr7:100494904-100494925

No.	Distal block	Cell Line	Cell type
1	chr7:100494043..100496246-chr7:100550371..100552219,2	K562	blood:
2	chr7:100491420..100497264-chr7:100607951..100612175,9	K562	blood:
3	chr7:100494599..100495240-chr7:100720850..100721501,2	MCF-7	breast:
4	chr7:100493649..100495175-chr7:100549463..100550982,2	MCF-7	breast:
5	chr7:100491799..100497264-chr7:100607837..100612175,9	K562	blood:
6	chr7:100494780..100495608-chr7:100609169..100610066,2	MCF-7	breast:
7	chr7:100494449..100495718-chr7:100608430..100610036,6	MCF-7	breast:
8	chr7:100493490..100497118-chr7:100701265..100703603,3	K562	blood:
9	chr7:100026330..100028591-chr7:100493941..100496922,3	K562	blood:
10	chr7:100492344..100495062-chr7:100726871..100729209,3	MCF-7	breast:
11	chr7:100026330..100028332-chr7:100493941..100495752,2	K562	blood:
12	chr7:100494655..100497277-chr7:100728768..100731587,2	K562	blood:
13	chr7:100494864..100496737-chr7:100607538..100610305,2	MCF-7	breast:
14	chr7:100491924..100495059-chr7:100886100..100889819,5	MCF-7	breast:
15	chr7:100492733..100496183-chr7:100699112..100703676,5	MCF-7	breast:

Variant related genes	Relation type
ACHE	TF binding region
ENSG00000078487	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000169894	Chromatin interaction
ENSG00000225946	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000222636	Chromatin interaction
ENSG00000214253	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 3 )

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

rs_ID	r²[population]
rs12666989	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12667888	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12705089	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12705090	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12705091	0.93[EUR][1000 genomes]
rs12705092	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12705095	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12705096	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13226502	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13226864	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13244629	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13245899	0.91[EUR][1000 genomes]
rs17881696	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17884589	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs314370	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs314373	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3757868	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6706	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS 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	92 gene(s)	inside rSNPs	diseases
2	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS 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	90 gene(s)	inside rSNPs	diseases
6	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
8	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS 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	89 gene(s)	inside rSNPs	diseases
9	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS 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	89 gene(s)	inside rSNPs	diseases
10	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
11	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS 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 miRNA target site	90 gene(s)	inside rSNPs	diseases
12	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
13	nsv888802	chr7:100484917-100495530	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
14	nsv888803	chr7:100486656-100497131	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
15	nsv888805	chr7:100486754-100498057	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
16	nsv888806	chr7:100488407-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
17	nsv888807	chr7:100490077-100498057	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv888808	chr7:100490981-100498057	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv888809	chr7:100491451-100495530	Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
20	nsv888810	chr7:100492127-100495530	Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
21	nsv888811	chr7:100492127-100497131	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
22	nsv888812	chr7:100492127-100498057	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
23	nsv888813	chr7:100492322-100495530	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv888814	chr7:100492357-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
25	nsv888815	chr7:100492357-100497131	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
26	nsv607970	chr7:100492493-100494949	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs17883557	ACHE	cis	Artery Tibial	GTEx
rs17883557	ACHE	cis	Artery Aorta	GTEx
rs17883557	ACHE	cis	Nerve Tibial	GTEx

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100491800-100495000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
2	chr7:100492200-100495000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:100492600-100495000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:100493400-100495200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
5	chr7:100493600-100495200	Bivalent/Poised TSS	HSMM	muscle
6	chr7:100493800-100495000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
7	chr7:100493800-100495200	Bivalent Enhancer	Placenta	Placenta
8	chr7:100494000-100495200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:100494000-100495200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
10	chr7:100494000-100495200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:100494000-100495200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
12	chr7:100494000-100495600	Bivalent Enhancer	Fetal Brain Male	brain
13	chr7:100494200-100495000	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:100494200-100495000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr7:100494200-100495000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:100494200-100495000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:100494200-100495000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:100494200-100495000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
19	chr7:100494200-100495000	Active TSS	Brain Hippocampus Middle	brain
20	chr7:100494200-100495000	Bivalent/Poised TSS	Left Ventricle	heart
21	chr7:100494200-100495200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
22	chr7:100494200-100495200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:100494200-100495200	Enhancers	Liver	Liver
24	chr7:100494200-100495200	Bivalent/Poised TSS	Brain Angular Gyrus	brain
25	chr7:100494200-100495200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr7:100494200-100495400	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr7:100494200-100495800	Bivalent Enhancer	Stomach Mucosa	stomach
28	chr7:100494400-100495000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
29	chr7:100494400-100495000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:100494400-100495000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
31	chr7:100494400-100495000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
32	chr7:100494400-100495000	Bivalent/Poised TSS	Primary T helper naive cells fromperipheralblood	blood
33	chr7:100494400-100495000	Bivalent/Poised TSS	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:100494400-100495000	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
35	chr7:100494400-100495000	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:100494400-100495000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
37	chr7:100494400-100495000	Active TSS	Brain Substantia Nigra	brain
38	chr7:100494400-100495000	Active TSS	Duodenum Mucosa	Duodenum
39	chr7:100494400-100495000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
40	chr7:100494400-100495000	Bivalent/Poised TSS	Esophagus	oesophagus
41	chr7:100494400-100495000	Bivalent/Poised TSS	Fetal Brain Female	brain
42	chr7:100494400-100495000	Bivalent/Poised TSS	Fetal Stomach	stomach
43	chr7:100494400-100495000	Bivalent/Poised TSS	Right Ventricle	heart
44	chr7:100494400-100495000	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
45	chr7:100494400-100495000	Flanking Bivalent TSS/Enh	Thymus	Thymus
46	chr7:100494400-100495000	Enhancers	Spleen	Spleen
47	chr7:100494400-100495000	Active TSS	K562	blood
48	chr7:100494400-100495000	Bivalent/Poised TSS	NHLF	lung
49	chr7:100494400-100495200	Active TSS	H9 Cell Line	embryonic stem cell
50	chr7:100494400-100495200	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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