Variant report

Variant	rs8128323
Chromosome Location	chr21:45208976-45208977
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	POLR2A	chr21:45208685-45210008	HepG2	liver:	n/a	n/a
2	HEY1	chr21:45208942-45209700	K562	blood:	n/a	n/a
3	PAX5	chr21:45208929-45209677	GM12878	blood:	n/a	chr21:45209263-45209272 chr21:45209301-45209310 chr21:45209265-45209274
4	POLR2A	chr21:45208954-45209941	K562	blood:	n/a	n/a
5	TAF1	chr21:45208952-45209491	A549	lung:	n/a	n/a
6	RPC155	chr21:45208096-45209406	K562	blood:	n/a	n/a
7	POLR2A	chr21:45208843-45209805	U87	brain:	n/a	n/a
8	POLR2A	chr21:45208890-45209856	ECC-1	luminal epithelium:	n/a	n/a
9	TAF1	chr21:45208918-45209842	ECC-1	luminal epithelium:	n/a	n/a
10	MAX	chr21:45208879-45210111	A549	lung:	n/a	chr21:45209747-45209757 chr21:45209747-45209757
11	E2F6	chr21:45208950-45209661	A549	lung:	n/a	chr21:45209332-45209342 chr21:45209305-45209314 chr21:45209257-45209266 chr21:45209251-45209260 chr21:45209245-45209254
12	CTCF	chr21:45208880-45209809	SK-N-SH	brain:	n/a	n/a
13	MAX	chr21:45208889-45210157	HepG2	liver:	n/a	chr21:45209747-45209757 chr21:45209747-45209757
14	MAX	chr21:45208902-45209985	SK-N-SH	brain:	n/a	chr21:45209747-45209757 chr21:45209747-45209757
15	POU2F2	chr21:45208931-45209690	GM12891	blood:	n/a	chr21:45209650-45209662
16	RUNX3	chr21:45208880-45209853	GM12878	blood:	n/a	n/a
17	CREB1	chr21:45208895-45209804	HepG2	liver:	n/a	n/a
18	CTCF	chr21:45208960-45209110	K562	blood:	n/a	n/a
19	STAT5A	chr21:45208898-45209580	K562	blood:	n/a	n/a
20	POLR2A	chr21:45208909-45209676	HepG2	liver:	n/a	n/a
21	POLR2A	chr21:45208976-45209779	PBDE	blood:	n/a	n/a
22	CREB1	chr21:45208900-45210044	K562	blood:	n/a	n/a
23	REST	chr21:45208958-45209580	A549	lung:	n/a	n/a
24	CREB1	chr21:45208897-45210135	HepG2	liver:	n/a	n/a
25	RCOR1	chr21:45208827-45209597	K562	blood:	n/a	n/a
26	POLR2A	chr21:45208953-45209945	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr21:45208955-45209372	GM12878	blood:	n/a	n/a
28	PAX5	chr21:45208889-45209870	GM12892	blood:	n/a	chr21:45209263-45209272 chr21:45209301-45209310 chr21:45209265-45209274
29	SP1	chr21:45208882-45209663	A549	lung:	n/a	chr21:45209650-45209660
30	MTA3	chr21:45208816-45210030	GM12878	blood:	n/a	n/a
31	POLR2A	chr21:45208939-45209967	GM12878	blood:	n/a	n/a
32	RPC155	chr21:45208468-45209102	Hela-S3	cervix:	n/a	n/a
33	HEY1	chr21:45208894-45209726	HepG2	liver:	n/a	n/a
34	CTCF	chr21:45208968-45209142	GM19240	blood:	n/a	n/a
35	E2F6	chr21:45208906-45209142	K562	blood:	n/a	n/a
36	MAX	chr21:45208919-45209993	Hela-S3	cervix:	n/a	chr21:45209747-45209757 chr21:45209747-45209757
37	POLR2A	chr21:45208903-45209655	PANC-1	pancreas:	n/a	n/a
38	E2F6	chr21:45208959-45209970	K562	blood:	n/a	chr21:45209332-45209342 chr21:45209305-45209314 chr21:45209703-45209713 chr21:45209811-45209820 chr21:45209257-45209266 chr21:45209251-45209260 chr21:45209245-45209254 chr21:45209812-45209822
39	POLR2A	chr21:45208960-45209705	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F6	chr21:45208958-45209945	H1-hESC	embryonic stem cell:	n/a	chr21:45209332-45209342 chr21:45209305-45209314 chr21:45209703-45209713 chr21:45209811-45209820 chr21:45209257-45209266 chr21:45209251-45209260 chr21:45209245-45209254 chr21:45209812-45209822
41	MYC	chr21:45208963-45210340	K562	blood:	n/a	chr21:45209747-45209757 chr21:45209747-45209757
42	TAF1	chr21:45208953-45209717	K562	blood:	n/a	n/a
43	POLR2A	chr21:45208898-45209938	K562	blood:	n/a	n/a
44	TAF1	chr21:45208885-45209712	H1-hESC	embryonic stem cell:	n/a	n/a
45	ZKSCAN1	chr21:45208839-45209621	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr21:45208911-45209725	PANC-1	pancreas:	n/a	n/a
47	UBTF	chr21:45208972-45209172	K562	blood:	n/a	n/a
48	EP300	chr21:45208949-45209851	ECC-1	luminal epithelium:	n/a	chr21:45209231-45209247 chr21:45209807-45209816 chr21:45209704-45209713 chr21:45209800-45209816
49	MAX	chr21:45208903-45209998	K562	blood:	n/a	chr21:45209747-45209757 chr21:45209747-45209757
50	MAX	chr21:45208905-45210347	MCF-7	breast:	n/a	chr21:45209747-45209757 chr21:45209747-45209757

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45208971-45209021	Caco-2	colon:	n/a
2	chr21:45208971-45209021	LNCaP	prostate:	n/a
3	chr21:45208971-45209021	AoSMC	blood vessel:	n/a
4	chr21:45208971-45209021	HRCEpiC	kidney:	n/a
5	chr21:45208971-45209021	BE2_C	brain:	n/a
6	chr21:45208971-45209021	HepG2	liver:	n/a
7	chr21:45208971-45209021	T-47D	breast:	n/a
8	chr21:45208971-45209021	GM19239	blood:	n/a
9	chr21:45208971-45209021	GM12892	blood:	n/a
10	chr21:45208971-45209021	HCM	heart:	n/a
11	chr21:45208971-45209021	SK-N-MC	brain:	n/a
12	chr21:45208971-45209021	SKMC	muscle:	n/a
13	chr21:45208971-45209021	NHDF-neo	bronchial:	n/a
14	chr21:45208971-45209021	SK-N-SH_RA	brain:	n/a
15	chr21:45208971-45209021	H1-hESC	embryonic stem cell:	embryo
16	chr21:45208971-45209021	ovcar-3	ovarian:	n/a
17	chr21:45208971-45209021	HCF	heart:	n/a
18	chr21:45208971-45209021	HRPEpiC	eye:	n/a
19	chr21:45208971-45209021	HL-60	blood:	n/a
20	chr21:45208971-45209021	AG09319	gingival:	n/a
21	chr21:45208971-45209021	AG04449	skin:	fetal
22	chr21:45208971-45209021	GM12891	blood:	n/a
23	chr21:45208971-45209021	HNPCEpiC	eye:	n/a
24	chr21:45208971-45209021	HMEC	breast:	n/a
25	chr21:45208971-45209021	NHBE	bronchial:	n/a
26	chr21:45208971-45209021	K562	blood:	n/a
27	chr21:45208971-45209021	Hepatocyte	liver:	n/a
28	chr21:45208971-45209021	PANC-1	pancreas:	n/a
29	chr21:45208971-45209021	PFSK-1	brain:	n/a
30	chr21:45208971-45209021	CMK	blood:	n/a
31	chr21:45208971-45209021	NT2-D1	testis:	n/a
32	chr21:45208971-45209021	AG10803	skin:	n/a
33	chr21:45208971-45209021	MCF-7	breast:	n/a
34	chr21:45208971-45209021	Hela-S3	cervix:	n/a
35	chr21:45208971-45209021	ProgFib	skin:	n/a
36	chr21:45208971-45209021	SAEC	small airway:	n/a
37	chr21:45208971-45209021	AG09309	skin:	n/a
38	chr21:45208971-45209021	GM06990	blood:	n/a
39	chr21:45208971-45209021	MCF10A-Er-Src	breast:	n/a
40	chr21:45208971-45209021	AG04450	lung:	fetal
41	chr21:45208971-45209021	HAEpiC	amniotic membrane:	n/a
42	chr21:45208971-45209021	HIPEpiC	eye:	n/a
43	chr21:45208971-45209021	PrEC	prostate:	n/a
44	chr21:45208971-45209021	A549	lung:	n/a
45	chr21:45208971-45209021	NB4	blood:	n/a
46	chr21:45208971-45209021	Jurkat	blood:	n/a
47	chr21:45208971-45209021	HEK293	kidney:	embryo
48	chr21:45208971-45209021	HCPEpiC	choroid plexus:	n/a
49	chr21:45208971-45209021	U87	brain:	n/a
50	chr21:45208971-45209021	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:45158615..45161441-chr21:45207897..45210708,2	K562	blood:
2	chr21:45159250..45162021-chr21:45208113..45211544,3	MCF-7	breast:
3	chr21:45207900..45209521-chr21:45431429..45433903,2	MCF-7	breast:
4	chr21:45207339..45211369-chr21:45429720..45433341,4	K562	blood:
5	chr21:45141091..45143140-chr21:45208651..45211403,2	K562	blood:
6	chr21:45136894..45141532-chr21:45205840..45211872,8	MCF-7	breast:
7	chr21:45130981..45133882-chr21:45206562..45209340,2	K562	blood:
8	chr21:45208647..45209350-chr3:12598128..12598853,2	MCF-7	breast:
9	chr21:45188049..45190841-chr21:45206908..45209310,2	MCF-7	breast:
10	chr21:45193334..45196312-chr21:45207752..45211007,4	MCF-7	breast:
11	chr21:45138000..45143848-chr21:45206375..45212489,9	MCF-7	breast:
12	chr21:45201612..45205256-chr21:45206995..45210818,5	MCF-7	breast:
13	chr21:45076259..45080839-chr21:45207005..45211007,4	MCF-7	breast:
14	chr21:45195743..45196721-chr21:45208905..45209461,2	MCF-7	breast:

Variant related genes	Relation type
RRP1	TF binding region
RRP1	CpG island
ENSG00000160207	Chromatin interaction
ENSG00000160209	Chromatin interaction
ENSG00000160218	Chromatin interaction
ENSG00000234030	Chromatin interaction
ENSG00000075975	Chromatin interaction
ENSG00000160213	Chromatin interaction
ENSG00000160208	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11089097	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1136072	0.89[EUR][1000 genomes]
rs11909278	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1537118	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1537120	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2070538	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2838364	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2838373	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2838376	0.80[AMR][1000 genomes]
rs2838379	0.80[AMR][1000 genomes]
rs2838380	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2838385	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2838391	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2838400	0.89[EUR][1000 genomes]
rs2838405	0.84[EUR][1000 genomes]
rs28759507	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3788072	0.85[AMR][1000 genomes]
rs4819314	0.95[ASN][1000 genomes]
rs55663506	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55825369	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55982230	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56387943	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60418573	0.96[ASN][1000 genomes]
rs62230077	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs62230079	0.85[AMR][1000 genomes]
rs6518321	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67676705	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7276362	0.81[EUR][1000 genomes]
rs7276547	0.86[EUR][1000 genomes]
rs8132984	0.82[EUR][1000 genomes]
rs915770	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9808695	0.81[AMR][1000 genomes]
rs9976535	0.92[ASN][1000 genomes]
rs9980220	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9984420	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531545	chr21:45095397-45395904	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv913876	chr21:45119629-45267193	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	esv2830066	chr21:45133868-45258047	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' 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 target site	44 gene(s)	inside rSNPs	diseases
4	nsv913879	chr21:45145286-45237039	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv913880	chr21:45145286-45263920	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv913881	chr21:45145286-45267193	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv470904	chr21:45151045-45258047	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv913882	chr21:45151874-45370715	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
9	nsv834107	chr21:45155325-45294546	Enhancers Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
10	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
11	nsv520305	chr21:45175958-45246326	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
12	nsv834108	chr21:45178037-45369641	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
13	nsv913883	chr21:45191139-45252838	Weak transcription Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
14	nsv913884	chr21:45191139-45255836	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
15	nsv544469	chr21:45194085-45257959	Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
16	esv3347263	chr21:45204424-45209222	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
17	nsv913885	chr21:45206355-45249474	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8128323	CSTB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45196800-45209000	Weak transcription	Aorta	Aorta
2	chr21:45204600-45209000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr21:45207200-45209000	Weak transcription	Lung	lung
4	chr21:45207200-45209400	Weak transcription	Spleen	Spleen
5	chr21:45207400-45209000	Weak transcription	Gastric	stomach
6	chr21:45208400-45209000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr21:45208400-45209400	Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr21:45208400-45209800	Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr21:45208400-45209800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr21:45208400-45210000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr21:45208400-45210200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr21:45208400-45210800	Active TSS	HSMM	muscle
13	chr21:45208600-45209000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
14	chr21:45208600-45209000	Flanking Active TSS	Primary B cells from peripheral blood	blood
15	chr21:45208600-45209000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
16	chr21:45208600-45209000	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr21:45208600-45209000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr21:45208600-45209000	Weak transcription	Fetal Brain Male	brain
19	chr21:45208600-45209000	Enhancers	Fetal Lung	lung
20	chr21:45208600-45209200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
21	chr21:45208600-45209400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr21:45208600-45209400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr21:45208600-45209800	Active TSS	Primary T killer memory cells from peripheral blood	blood
24	chr21:45208600-45209800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr21:45208600-45209800	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr21:45208600-45209800	Active TSS	HepG2	liver
27	chr21:45208600-45210000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr21:45208600-45210000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr21:45208600-45210000	Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr21:45208600-45210000	Active TSS	Brain Angular Gyrus	brain
31	chr21:45208600-45210000	Active TSS	Brain Germinal Matrix	brain
32	chr21:45208600-45210000	Active TSS	Brain Hippocampus Middle	brain
33	chr21:45208600-45210000	Active TSS	Brain Substantia Nigra	brain
34	chr21:45208600-45210000	Active TSS	Duodenum Mucosa	Duodenum
35	chr21:45208600-45210000	Active TSS	Duodenum Smooth Muscle	Duodenum
36	chr21:45208600-45210000	Active TSS	Fetal Intestine Small	intestine
37	chr21:45208600-45210000	Active TSS	HUVEC	blood vessel
38	chr21:45208600-45210000	Active TSS	NHEK	skin
39	chr21:45208600-45210000	Active TSS	Osteobl	bone
40	chr21:45208600-45210200	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr21:45208600-45210200	Active TSS	Muscle Satellite Cultured Cells	--
42	chr21:45208600-45210200	Active TSS	Fetal Intestine Large	intestine
43	chr21:45208600-45210200	Active TSS	Hela-S3	cervix
44	chr21:45208600-45210200	Active TSS	K562	blood
45	chr21:45208600-45210200	Active TSS	NHLF	lung
46	chr21:45208600-45210400	Active TSS	GM12878-XiMat	blood
47	chr21:45208600-45210400	Active TSS	HSMMtube	muscle
48	chr21:45208600-45210600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr21:45208600-45210800	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr21:45208600-45210800	Active TSS	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links