Variant report

Variant	rs4319008
Chromosome Location	chr7:99698015-99698016
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:368)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:99697938-99698548	A549	lung:	n/a	chr7:99698416-99698425 chr7:99698400-99698409
2	GATA3	chr7:99697897-99698749	MCF-7	breast:	n/a	n/a
3	BCLAF1	chr7:99697803-99698570	GM12878	blood:	n/a	chr7:99698416-99698425 chr7:99698400-99698409
4	CEBPD	chr7:99698005-99698629	HepG2	liver:	n/a	n/a
5	HEY1	chr7:99697723-99699845	K562	blood:	n/a	n/a
6	EGR1	chr7:99697928-99698525	GM12878	blood:	n/a	chr7:99698400-99698409 chr7:99698416-99698425 chr7:99698504-99698514
7	SIN3AK20	chr7:99697831-99698641	H1-hESC	embryonic stem cell:	n/a	n/a
8	SPI1	chr7:99698004-99698577	HL-60	blood:	n/a	n/a
9	GABPA	chr7:99697838-99698701	SK-N-SH	brain:	n/a	n/a
10	TBL1XR1	chr7:99697982-99698543	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:99697924-99699712	GM12878	blood:	n/a	n/a
12	POLR2A	chr7:99697920-99699673	GM12891	blood:	n/a	n/a
13	POLR2A	chr7:99694417-99699772	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr7:99697890-99699623	GM12878	blood:	n/a	chr7:99698390-99698400
15	MYC	chr7:99697990-99699667	K562	blood:	n/a	chr7:99699037-99699048 chr7:99699038-99699047 chr7:99698505-99698515 chr7:99699036-99699045
16	CHD1	chr7:99697355-99699100	H1-hESC	embryonic stem cell:	n/a	chr7:99698390-99698400
17	POLR2A	chr7:99697846-99699795	H1-hESC	embryonic stem cell:	n/a	n/a
18	RELA	chr7:99697882-99699593	GM19193	blood:	n/a	n/a
19	MAX	chr7:99697838-99699753	ECC-1	luminal epithelium:	n/a	chr7:99699037-99699048 chr7:99699038-99699047 chr7:99698505-99698515 chr7:99699036-99699045
20	MAX	chr7:99697829-99698530	H1-hESC	embryonic stem cell:	n/a	chr7:99698505-99698515
21	FOXA1	chr7:99697855-99698596	HepG2	liver:	n/a	n/a
22	MAZ	chr7:99697948-99698554	HepG2	liver:	n/a	chr7:99698505-99698515
23	POLR2A	chr7:99697969-99699757	GM12892	blood:	n/a	n/a
24	POLR2A	chr7:99697867-99699882	GM12892	blood:	n/a	n/a
25	MAX	chr7:99697858-99699799	SK-N-SH	brain:	n/a	chr7:99699037-99699048 chr7:99699038-99699047 chr7:99698505-99698515 chr7:99699036-99699045
26	POLR2A	chr7:99697747-99699738	GM12878	blood:	n/a	n/a
27	EGR1	chr7:99697905-99698644	K562	blood:	n/a	chr7:99698400-99698409 chr7:99698630-99698643 chr7:99698416-99698425 chr7:99698504-99698514
28	CREB1	chr7:99697882-99699907	HepG2	liver:	n/a	n/a
29	FOXM1	chr7:99697928-99698570	GM12878	blood:	n/a	n/a
30	MYC	chr7:99697655-99698838	A549	lung:	n/a	chr7:99698505-99698515
31	REST	chr7:99697961-99698636	SK-N-SH	brain:	n/a	n/a
32	TAF1	chr7:99698006-99699403	Hela-S3	cervix:	n/a	n/a
33	ELF1	chr7:99697960-99698598	HepG2	liver:	n/a	n/a
34	POLR2A	chr7:99697963-99699667	GM12878	blood:	n/a	n/a
35	POLR2A	chr7:99697762-99700065	H1-hESC	embryonic stem cell:	n/a	n/a
36	TEAD4	chr7:99697935-99699413	K562	blood:	n/a	n/a
37	ATF2	chr7:99697984-99698635	GM12878	blood:	n/a	n/a
38	POLR2A	chr7:99697901-99699802	ECC-1	luminal epithelium:	n/a	n/a
39	POLR2A	chr7:99697986-99699733	GM12891	blood:	n/a	n/a
40	GABPA	chr7:99697958-99698656	K562	blood:	n/a	n/a
41	REST	chr7:99697986-99698657	K562	blood:	n/a	n/a
42	MAX	chr7:99697774-99699937	HCT-116	colon:	n/a	chr7:99699037-99699048 chr7:99699038-99699047 chr7:99698505-99698515 chr7:99699036-99699045
43	POLR2A	chr7:99697978-99699805	ECC-1	luminal epithelium:	n/a	n/a
44	TEAD4	chr7:99697950-99698581	H1-hESC	embryonic stem cell:	n/a	n/a
45	SIN3AK20	chr7:99697959-99698573	SK-N-SH	brain:	n/a	n/a
46	USF1	chr7:99697974-99698642	SK-N-SH_RA	brain:	n/a	n/a
47	CHD2	chr7:99697802-99699336	H1-hESC	embryonic stem cell:	n/a	chr7:99698390-99698400
48	SP1	chr7:99697810-99699951	HCT-116	colon:	n/a	chr7:99698383-99698397 chr7:99698758-99698767 chr7:99699063-99699084
49	POLR2A	chr7:99697989-99699921	GM12878	blood:	n/a	n/a
50	CREB1	chr7:99697900-99699874	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99697978-99698028	SK-N-SH	brain:	n/a
2	chr7:99697978-99698028	RPTEC	kidney:	n/a
3	chr7:99697978-99698028	BJ	skin:	n/a
4	chr7:99697978-99698028	AoSMC	blood vessel:	n/a
5	chr7:99697978-99698028	HRE	kidney:	n/a
6	chr7:99697978-99698028	HCF	heart:	n/a
7	chr7:99697978-99698028	HAEpiC	amniotic membrane:	n/a
8	chr7:99697978-99698028	NT2-D1	testis:	n/a
9	chr7:99697978-99698028	BE2_C	brain:	n/a
10	chr7:99697978-99698028	HEK293	kidney:	embryo
11	chr7:99697978-99698028	NH-A	brain:	n/a
12	chr7:99697978-99698028	AG04450	lung:	fetal
13	chr7:99697978-99698028	A549	lung:	n/a
14	chr7:99697978-99698028	HMEC	breast:	n/a
15	chr7:99697978-99698028	IMR90	lung:	fetal
16	chr7:99697978-99698028	HCM	heart:	n/a
17	chr7:99697978-99698028	MCF10A-Er-Src	breast:	n/a
18	chr7:99697978-99698028	PrEC	prostate:	n/a
19	chr7:99697978-99698028	HCPEpiC	choroid plexus:	n/a
20	chr7:99697978-99698028	H1-hESC	embryonic stem cell:	embryo
21	chr7:99697978-99698028	HRPEpiC	eye:	n/a
22	chr7:99697978-99698028	T-47D	breast:	n/a
23	chr7:99697978-99698028	SKMC	muscle:	n/a
24	chr7:99697978-99698028	AG09319	gingival:	n/a
25	chr7:99697978-99698028	GM12891	blood:	n/a
26	chr7:99697978-99698028	LNCaP	prostate:	n/a
27	chr7:99697978-99698028	AG04449	skin:	fetal
28	chr7:99697978-99698028	NHBE	bronchial:	n/a
29	chr7:99697978-99698028	AG10803	skin:	n/a
30	chr7:99697978-99698028	GM06990	blood:	n/a
31	chr7:99697978-99698028	HIPEpiC	eye:	n/a
32	chr7:99697978-99698028	SAEC	small airway:	n/a
33	chr7:99697978-99698028	MCF-7	breast:	n/a
34	chr7:99697978-99698028	CMK	blood:	n/a
35	chr7:99697978-99698028	GM12892	blood:	n/a
36	chr7:99697978-99698028	ECC-1	luminal epithelium:	n/a
37	chr7:99697978-99698028	Caco-2	colon:	n/a
38	chr7:99697978-99698028	K562	blood:	n/a
39	chr7:99697978-99698028	U87	brain:	n/a
40	chr7:99697978-99698028	ovcar-3	ovarian:	n/a
41	chr7:99697978-99698028	HepG2	liver:	n/a
42	chr7:99697978-99698028	ProgFib	skin:	n/a
43	chr7:99697978-99698028	PFSK-1	brain:	n/a
44	chr7:99697978-99698028	NB4	blood:	n/a
45	chr7:99697978-99698028	HCT-116	colon:	n/a
46	chr7:99697978-99698028	NHDF-neo	bronchial:	n/a
47	chr7:99697978-99698028	HUVEC	blood vessel:	n/a
48	chr7:99697978-99698028	AG09309	skin:	n/a
49	chr7:99697978-99698028	HL-60	blood:	n/a
50	chr7:99697978-99698028	Jurkat	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99696160..99700887-chr7:99753963..99757907,5	K562	blood:
2	chr12:7053195..7053882-chr7:99697963..99698664,2	Hela-S3	cervix:
3	chr7:99697399..99699503-chr7:99751252..99753483,2	MCF-7	breast:
4	chr7:99695452..99699124-chr7:100025277..100027831,3	MCF-7	breast:
5	chr7:99696160..99699295-chr7:99753963..99757907,4	K562	blood:
6	chr7:99612390..99616211-chr7:99697108..99699457,4	K562	blood:
7	chr7:99645952..99651427-chr7:99695296..99699701,5	K562	blood:
8	chr7:99696789..99700792-chr7:100024893..100031468,10	K562	blood:
9	chr16:75498163..75498768-chr7:99697963..99698902,2	Hela-S3	cervix:
10	chr7:99697112..99700279-chr7:100024243..100028129,6	MCF-7	breast:
11	chr7:99588575..99590179-chr7:99697467..99700310,2	K562	blood:
12	chr7:99036383..99037983-chr7:99697616..99700262,2	MCF-7	breast:
13	chr7:99645798..99648883-chr7:99696634..99699359,3	MCF-7	breast:
14	chr7:99576315..99578805-chr7:99697574..99699659,2	MCF-7	breast:
15	chr7:99004495..99006339-chr7:99697031..99698874,2	K562	blood:
16	chr7:99697813..99699530-chr7:99754761..99757399,3	MCF-7	breast:
17	chr14:102430111..102432815-chr7:99697552..99699844,2	MCF-7	breast:
18	chr7:99697347..99700775-chr7:100198565..100202321,3	MCF-7	breast:
19	chr7:99697080..99699701-chr7:100805624..100808540,2	MCF-7	breast:
20	chr7:99697950..99701090-chr7:99746543..99749524,3	MCF-7	breast:
21	chr7:99516652..99519879-chr7:99696878..99699951,3	MCF-7	breast:
22	chr7:99646207..99647783-chr7:99696961..99699503,2	MCF-7	breast:
23	chr7:99697437..99703178-chr7:100024624..100029482,10	K562	blood:
24	chr7:99612390..99617445-chr7:99697108..99699685,5	K562	blood:
25	chr11:70049171..70049741-chr7:99697780..99698499,2	Hela-S3	cervix:
26	chr7:99696898..99700086-chr7:99750657..99754674,4	MCF-7	breast:
27	chr7:99697181..99698969-chr7:99947423..99949421,2	K562	blood:
28	chr7:99061682..99064704-chr7:99696557..99699487,3	K562	blood:
29	chr7:99035431..99038374-chr7:99696976..99699327,2	K562	blood:
30	chr7:99696142..99700081-chr7:99754300..99760427,7	MCF-7	breast:
31	chr7:99588477..99590075-chr7:99697467..99699544,2	K562	blood:
32	chr17:61698893..61701536-chr7:99697236..99699557,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAF6-2	chr7:99697637-99698016	NONHSAT122317

No data

Variant related genes	Relation type
MCM7	TF binding region
AP4M1	TF binding region
MCM7	CpG island
AP4M1	CpG island
ENSG00000168040	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000166529	Chromatin interaction
ENSG00000197102	Chromatin interaction
ENSG00000272173	Chromatin interaction
ENSG00000272752	Chromatin interaction
ENSG00000235713	Chromatin interaction
ENSG00000261717	Chromatin interaction
ENSG00000166822	Chromatin interaction
ENSG00000188186	Chromatin interaction
ENSG00000106333	Chromatin interaction
ENSG00000146833	Chromatin interaction
ENSG00000106245	Chromatin interaction
ENSG00000241468	Chromatin interaction
ENSG00000248919	Chromatin interaction
ENSG00000106244	Chromatin interaction
ENSG00000146826	Chromatin interaction
ENSG00000160917	Chromatin interaction
ENSG00000106261	Chromatin interaction
ENSG00000128564	Chromatin interaction
ENSG00000224729	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000266154	Chromatin interaction
ENSG00000198909	Chromatin interaction
ENSG00000214313	Chromatin interaction
ENSG00000106246	Chromatin interaction
ENSG00000111678	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 7 )

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

rs_ID	r²[population]
rs1130958	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13228844	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17447058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17447273	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1859305	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[TSI][hapmap];0.91[ASN][1000 genomes]
rs2272346	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2307355	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2525557	1.00[MEX][hapmap];0.83[TSI][hapmap]
rs41280962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4134891	1.00[MEX][hapmap];1.00[TSI][hapmap]
rs4134911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4134914	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4134925	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4134927	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4729565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4928	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6960542	1.00[CHB][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829865	chr7:99430678-99755141	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1131 gene(s)	inside rSNPs	diseases
2	esv1830649	chr7:99430678-99755141	Strong transcription Flanking Active TSS Weak transcription Enhancers 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	1131 gene(s)	inside rSNPs	diseases
3	nsv534298	chr7:99478011-99886076	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1132 gene(s)	inside rSNPs	diseases
4	nsv469687	chr7:99572543-99755141	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1115 gene(s)	inside rSNPs	diseases
5	nsv482601	chr7:99572543-99755141	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1115 gene(s)	inside rSNPs	diseases
6	nsv607931	chr7:99664817-99796146	Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1097 gene(s)	inside rSNPs	diseases
7	esv1798486	chr7:99689883-99930879	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers 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	1085 gene(s)	inside rSNPs	diseases
8	esv1833059	chr7:99689883-99930879	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1085 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs4319008	PCOLCE-AS1	cis	Nerve Tibial	GTEx
rs4319008	BUD31	cis	lymphoblastoid	GTEx
rs4319008	COPS6	Cis_1M	lymphoblastoid	RTeQTL
rs4319008	MBLAC1	cis	lymphoblastoid	seeQTL
rs4319008	PCOLCE	cis	Nerve Tibial	GTEx
rs4319008	LOC255374	cis	multi-tissue	Pritchard
rs4319008	COPS6	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99696200-99698400	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr7:99696600-99698200	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
3	chr7:99697200-99698200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr7:99697200-99698200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
5	chr7:99697200-99698400	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
6	chr7:99697200-99700200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:99697400-99698200	Flanking Active TSS	Primary B cells from cord blood	blood
8	chr7:99697400-99698400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:99697400-99700200	Active TSS	Ovary	ovary
10	chr7:99697600-99698200	Active TSS	Right Atrium	heart
11	chr7:99697600-99698600	Active TSS	Brain Germinal Matrix	brain
12	chr7:99697600-99698600	Active TSS	Fetal Muscle Trunk	muscle
13	chr7:99697600-99699600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:99697600-99699600	Active TSS	Colonic Mucosa	Colon
15	chr7:99697600-99699800	Active TSS	Fetal Brain Male	brain
16	chr7:99697600-99699800	Active TSS	Spleen	Spleen
17	chr7:99697600-99700000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:99697600-99700000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:99697600-99700000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:99697600-99700000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:99697600-99700000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:99697600-99700000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr7:99697600-99700000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:99697600-99700000	Active TSS	Aorta	Aorta
25	chr7:99697600-99700000	Active TSS	Esophagus	oesophagus
26	chr7:99697600-99700000	Active TSS	Fetal Brain Female	brain
27	chr7:99697600-99700000	Active TSS	Fetal Intestine Large	intestine
28	chr7:99697600-99700000	Active TSS	Gastric	stomach
29	chr7:99697600-99700000	Active TSS	Left Ventricle	heart
30	chr7:99697600-99700000	Active TSS	Lung	lung
31	chr7:99697600-99700000	Active TSS	Placenta Amnion	Placenta Amnion
32	chr7:99697600-99700000	Active TSS	Psoas Muscle	Psoas
33	chr7:99697600-99700000	Active TSS	Right Ventricle	heart
34	chr7:99697600-99700000	Active TSS	Thymus	Thymus
35	chr7:99697600-99700000	Active TSS	GM12878-XiMat	blood
36	chr7:99697600-99700000	Active TSS	HSMMtube	muscle
37	chr7:99697600-99700000	Active TSS	NHDF-Ad	bronchial
38	chr7:99697600-99700200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr7:99697600-99700200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:99697600-99700200	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr7:99697600-99700200	Active TSS	HSMM	muscle
42	chr7:99697600-99700400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr7:99697600-99700400	Active TSS	Fetal Kidney	kidney
44	chr7:99697600-99700600	Active TSS	H9 Cell Line	embryonic stem cell
45	chr7:99697800-99698200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
46	chr7:99697800-99698200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr7:99697800-99698400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:99697800-99698400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:99697800-99698600	Active TSS	Muscle Satellite Cultured Cells	--
50	chr7:99697800-99698600	Active TSS	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links