Variant report

Variant	rs2239704
Chromosome Location	chr6:31540141-31540142
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:99)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:99 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:31539711-31540627	GM12878	blood:	n/a	n/a
2	PAX5	chr6:31539655-31540555	GM12878	blood:	n/a	chr6:31539767-31539776
3	POLR2A	chr6:31539586-31540519	GM12878	blood:	n/a	n/a
4	POLR2A	chr6:31539699-31541638	GM15510	blood:	n/a	n/a
5	RUNX3	chr6:31539442-31540862	GM12878	blood:	n/a	n/a
6	ELF1	chr6:31539770-31540688	GM12878	blood:	n/a	n/a
7	RUNX3	chr6:31539519-31541026	GM12878	blood:	n/a	n/a
8	RELA	chr6:31539747-31540767	GM10847	blood:	n/a	n/a
9	ELF1	chr6:31539676-31541034	GM12878	blood:	n/a	n/a
10	CTCF	chr6:31540125-31540171	GM19238	blood:	n/a	n/a
11	POLR2A	chr6:31539710-31540863	GM12878	blood:	n/a	n/a
12	POU2F2	chr6:31539968-31540266	GM12878	blood:	n/a	n/a
13	POLR2A	chr6:31539762-31540800	Raji	blood:	n/a	n/a
14	YY1	chr6:31539939-31540479	GM12878	blood:	n/a	chr6:31540457-31540471
15	TCF12	chr6:31539734-31540365	GM12878	blood:	n/a	chr6:31539754-31539764
16	POLR2A	chr6:31539991-31540388	GM12878	blood:	n/a	n/a
17	NFIC	chr6:31539651-31540560	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:31539705-31540525	GM12878	blood:	n/a	n/a
19	RCOR1	chr6:31539837-31540236	GM12878	blood:	n/a	n/a
20	SMC3	chr6:31539909-31540466	GM12878	blood:	n/a	chr6:31539997-31540007
21	POLR2A	chr6:31539444-31550290	GM12892	blood:	n/a	n/a
22	EBF1	chr6:31539793-31540883	GM12878	blood:	n/a	n/a
23	TBP	chr6:31539848-31540388	GM12878	blood:	n/a	n/a
24	POLR2A	chr6:31539494-31550471	GM12892	blood:	n/a	n/a
25	POLR2A	chr6:31539573-31540769	GM12892	blood:	n/a	n/a
26	CHD1	chr6:31539754-31540365	GM12878	blood:	n/a	n/a
27	CTCF	chr6:31540040-31540190	GM12867	blood:	n/a	n/a
28	MTA3	chr6:31539044-31550840	GM12878	blood:	n/a	n/a
29	PML	chr6:31539100-31540711	GM12878	blood:	n/a	chr6:31539674-31539682
30	BCLAF1	chr6:31539845-31540535	GM12878	blood:	n/a	chr6:31539964-31539973 chr6:31539999-31540012 chr6:31539882-31539895
31	RELA	chr6:31539439-31540774	GM18951	blood:	n/a	n/a
32	POLR2A	chr6:31539714-31540962	GM19099	blood:	n/a	n/a
33	TCF12	chr6:31539965-31540357	GM12878	blood:	n/a	n/a
34	ATF2	chr6:31539680-31540596	GM12878	blood:	n/a	n/a
35	RELA	chr6:31539492-31540764	GM12892	blood:	n/a	n/a
36	BCL11A	chr6:31539993-31540379	GM12878	blood:	n/a	chr6:31539999-31540012
37	RELA	chr6:31539149-31540926	GM12891	blood:	n/a	n/a
38	RELA	chr6:31539494-31540694	GM19099	blood:	n/a	n/a
39	POLR2A	chr6:31539679-31550540	GM12892	blood:	n/a	n/a
40	POLR2A	chr6:31539740-31540967	GM18526	blood:	n/a	n/a
41	TBL1XR1	chr6:31539901-31540495	GM12878	blood:	n/a	n/a
42	YY1	chr6:31539813-31540667	GM12878	blood:	n/a	chr6:31540457-31540471
43	PBX3	chr6:31540094-31540374	GM12878	blood:	n/a	n/a
44	TAF1	chr6:31540018-31540265	GM12891	blood:	n/a	n/a
45	PAX5	chr6:31540062-31540391	GM12878	blood:	n/a	n/a
46	PML	chr6:31539880-31540360	GM12878	blood:	n/a	n/a
47	ZEB1	chr6:31539798-31540763	GM12878	blood:	n/a	chr6:31539935-31539943 chr6:31539934-31539943 chr6:31540612-31540625
48	BCLAF1	chr6:31539592-31540679	GM12878	blood:	n/a	chr6:31539964-31539973 chr6:31539999-31540012 chr6:31539882-31539895
49	POLR2A	chr6:31539661-31540809	GM12878	blood:	n/a	n/a
50	TAF1	chr6:31539795-31540520	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31540121-31540171	HEK293	kidney:	embryo
2	chr6:31540136-31540186	PFSK-1	brain:	n/a
3	chr6:31540136-31540186	SK-N-SH_RA	brain:	n/a
4	chr6:31540114-31540164	T-47D	breast:	n/a
5	chr6:31540121-31540171	T-47D	breast:	n/a
6	chr6:31540114-31540164	HEK293	kidney:	embryo
7	chr6:31540136-31540186	HNPCEpiC	eye:	n/a
8	chr6:31540136-31540186	U87	brain:	n/a
9	chr6:31540114-31540164	H1-hESC	embryonic stem cell:	embryo
10	chr6:31540121-31540171	HCM	heart:	n/a
11	chr6:31540114-31540164	NHBE	bronchial:	n/a
12	chr6:31540114-31540164	SKMC	muscle:	n/a
13	chr6:31540121-31540171	U87	brain:	n/a
14	chr6:31540114-31540164	HRPEpiC	eye:	n/a
15	chr6:31540114-31540164	HMEC	breast:	n/a
16	chr6:31540121-31540171	BJ	skin:	n/a
17	chr6:31540136-31540186	K562	blood:	n/a
18	chr6:31540136-31540186	IMR90	lung:	fetal
19	chr6:31540114-31540164	Caco-2	colon:	n/a
20	chr6:31540121-31540171	RPTEC	kidney:	n/a
21	chr6:31540121-31540171	Jurkat	blood:	n/a
22	chr6:31540114-31540164	U87	brain:	n/a
23	chr6:31540136-31540186	HCM	heart:	n/a
24	chr6:31540114-31540164	Hela-S3	cervix:	n/a
25	chr6:31540114-31540164	HCT-116	colon:	n/a
26	chr6:31540121-31540171	HRCEpiC	kidney:	n/a
27	chr6:31540136-31540186	HRE	kidney:	n/a
28	chr6:31540121-31540171	GM19239	blood:	n/a
29	chr6:31540114-31540164	NH-A	brain:	n/a
30	chr6:31540114-31540164	SK-N-SH_RA	brain:	n/a
31	chr6:31540121-31540171	ECC-1	luminal epithelium:	n/a
32	chr6:31540136-31540186	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:31540136-31540186	HRCEpiC	kidney:	n/a
34	chr6:31540121-31540171	GM12892	blood:	n/a
35	chr6:31540114-31540164	HRCEpiC	kidney:	n/a
36	chr6:31540136-31540186	PrEC	prostate:	n/a
37	chr6:31540114-31540164	HEEpiC	esophagus:	n/a
38	chr6:31540136-31540186	HCF	heart:	n/a
39	chr6:31540136-31540186	A549	lung:	n/a
40	chr6:31540121-31540171	SKMC	muscle:	n/a
41	chr6:31540114-31540164	ProgFib	skin:	n/a
42	chr6:31540114-31540164	AoSMC	blood vessel:	n/a
43	chr6:31540114-31540164	HCM	heart:	n/a
44	chr6:31540136-31540186	HAEpiC	amniotic membrane:	n/a
45	chr6:31540121-31540171	NT2-D1	testis:	n/a
46	chr6:31540114-31540164	AG04449	skin:	fetal
47	chr6:31540136-31540186	NB4	blood:	n/a
48	chr6:31540121-31540171	ProgFib	skin:	n/a
49	chr6:31540136-31540186	MCF10A-Er-Src	breast:	n/a
50	chr6:31540121-31540171	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:31539772..31542619-chr6:31581316..31584667,3	K562	blood:
2	chr6:31504619..31508588-chr6:31538806..31541615,4	K562	blood:
3	chr6:31504619..31510971-chr6:31539361..31543067,6	K562	blood:

No data

Variant related genes	Relation type
TNF	TF binding region
TNF	CpG island
ENSG00000265236	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204472	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 7 )

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

rs_ID	r²[population]
rs1121800	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2071590	0.80[AMR][1000 genomes]
rs2516390	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2516391	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2516479	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2523500	0.89[AMR][1000 genomes]
rs2844483	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2844484	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2844485	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2844486	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2857602	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2857710	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3094595	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3135042	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3135043	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs746868	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs928815	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
2	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
3	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
4	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer 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	250 gene(s)	inside rSNPs	diseases
13	esv2757162	chr6:31353329-31542308	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
14	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
15	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
16	nsv470809	chr6:31496915-31544189	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
17	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription 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 miRNA target site	206 gene(s)	inside rSNPs	diseases
18	nsv462870	chr6:31528130-31544189	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
19	nsv601941	chr6:31528130-31544189	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs2239704	XXbac-BPG248L24.12	cis	Whole Blood	GTEx
rs2239704	HLA-DRB5	cis	parietal	SCAN
rs2239704	TEAD3	cis	cerebellum	SCAN
rs2239704	DEF6	cis	parietal	SCAN
rs2239704	HIST1H3I	cis	cerebellum	SCAN
rs2239704	HIST1H1B	cis	cerebellum	SCAN
rs2239704	HLA-DRB5	cis	lymphoblastoid	GTEx

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31528600-31541200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:31529000-31541200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:31535800-31541200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:31536000-31546200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr6:31536000-31548400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:31536200-31541400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr6:31536400-31541200	Weak transcription	Spleen	Spleen
8	chr6:31536600-31544200	Weak transcription	K562	blood
9	chr6:31537400-31542200	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr6:31537400-31542800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:31537600-31542000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr6:31538000-31542400	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr6:31538200-31541200	Weak transcription	HSMMtube	muscle
14	chr6:31538600-31541000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr6:31538600-31541400	Enhancers	Primary hematopoietic stem cells	blood
16	chr6:31539000-31543200	Flanking Active TSS	GM12878-XiMat	blood
17	chr6:31539200-31540200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
18	chr6:31539200-31540200	Enhancers	Small Intestine	intestine
19	chr6:31539200-31540600	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr6:31539200-31541000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr6:31539400-31540800	Flanking Active TSS	Primary B cells from peripheral blood	blood
22	chr6:31539400-31540800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
23	chr6:31539400-31540800	Active TSS	Duodenum Mucosa	Duodenum
24	chr6:31539400-31540800	Flanking Active TSS	Fetal Thymus	thymus
25	chr6:31539400-31541000	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr6:31539400-31541000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr6:31539600-31541000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:31539800-31540200	Bivalent/Poised TSS	HepG2	liver
29	chr6:31539800-31540400	Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr6:31539800-31540400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr6:31539800-31540600	Active TSS	Primary T cells from cord blood	blood
32	chr6:31539800-31540800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:31540000-31540200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr6:31540000-31540200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
35	chr6:31540000-31540200	Transcr. at gene 5' and 3'	Thymus	Thymus
36	chr6:31540000-31540400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr6:31540000-31540400	Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr6:31540000-31540400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:31540000-31540400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
40	chr6:31540000-31540400	Active TSS	Esophagus	oesophagus
41	chr6:31540000-31540400	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr6:31540000-31540600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:31540000-31540600	Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr6:31540000-31540600	Active TSS	Rectal Mucosa Donor 29	rectum

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