Variant report

Variant	rs12884809
Chromosome Location	chr14:104095320-104095321
allele	A/G
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	JUN	chr14:104095300-104095623	HepG2	liver:	n/a	chr14:104095470-104095483
2	POLR2A	chr14:104094191-104096591	IMR90	lung:	n/a	n/a
3	TBP	chr14:104094298-104095879	H1-hESC	embryonic stem cell:	n/a	n/a
4	MXI1	chr14:104093880-104096688	IMR90	lung:	n/a	n/a
5	POLR2A	chr14:104094388-104095853	HUVEC	blood vessel:	n/a	n/a
6	MAZ	chr14:104094425-104096619	GM12878	blood:	n/a	n/a
7	POLR2A	chr14:104094626-104096416	NB4	blood:	n/a	n/a
8	TEAD4	chr14:104095269-104095659	K562	blood:	n/a	n/a
9	TAF7	chr14:104095002-104095937	H1-hESC	embryonic stem cell:	n/a	n/a
10	GTF2F1	chr14:104095316-104095501	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr14:104094508-104096467	GM12892	blood:	n/a	n/a
12	MAX	chr14:104094298-104095890	A549	lung:	n/a	n/a
13	YY1	chr14:104095233-104095919	H1-hESC	embryonic stem cell:	n/a	chr14:104095542-104095564 chr14:104095554-104095568 chr14:104095542-104095552 chr14:104095256-104095270 chr14:104095541-104095553
14	SIN3AK20	chr14:104095270-104096058	SK-N-SH	brain:	n/a	n/a
15	JUN	chr14:104095307-104095596	H1-hESC	embryonic stem cell:	n/a	chr14:104095470-104095483
16	FOXA1	chr14:104095298-104095604	T-47D	breast:	n/a	n/a
17	POLR2A	chr14:104094507-104096548	GM12878	blood:	n/a	n/a
18	POU2F2	chr14:104095181-104095820	GM12878	blood:	n/a	n/a
19	POLR2A	chr14:104094478-104096182	GM12878	blood:	n/a	n/a
20	SIN3AK20	chr14:104095103-104096515	PANC-1	pancreas:	n/a	n/a
21	POLR2A	chr14:104094360-104095985	HCT-116	colon:	n/a	n/a
22	POLR2A	chr14:104095165-104095927	GM12892	blood:	n/a	n/a
23	POLR2A	chr14:104095056-104096067	MCF-7	breast:	n/a	n/a
24	TAF1	chr14:104095274-104095678	SK-N-SH	brain:	n/a	n/a
25	POLR2A	chr14:104094445-104096315	MCF10A-Er-Src	breast:	n/a	n/a
26	TCF3	chr14:104095285-104095863	GM12878	blood:	n/a	n/a
27	TAF1	chr14:104095257-104095750	PFSK-1	brain:	n/a	n/a
28	POLR2A	chr14:104094382-104096602	HUVEC	blood vessel:	n/a	n/a
29	RAD21	chr14:104094513-104095909	IMR90	lung:	n/a	chr14:104095120-104095133 chr14:104095811-104095824 chr14:104095246-104095260
30	PBX3	chr14:104095304-104095712	A549	lung:	n/a	n/a
31	MAX	chr14:104095237-104095933	NB4	blood:	n/a	n/a
32	MAX	chr14:104094462-104095885	A549	lung:	n/a	n/a
33	POLR2A	chr14:104095125-104096061	GM12891	blood:	n/a	n/a
34	POLR2A	chr14:104094369-104096083	H1-hESC	embryonic stem cell:	n/a	n/a
35	CCNT2	chr14:104094413-104096405	K562	blood:	n/a	chr14:104095108-104095117 chr14:104094458-104094478 chr14:104094504-104094513 chr14:104095293-104095302 chr14:104095447-104095456
36	CREB1	chr14:104095171-104095887	K562	blood:	n/a	n/a
37	RCOR1	chr14:104095303-104095737	HepG2	liver:	n/a	n/a
38	MXI1	chr14:104094125-104097496	SK-N-SH	brain:	n/a	n/a
39	ZNF143	chr14:104095285-104095728	Hela-S3	cervix:	n/a	chr14:104095394-104095412
40	MAX	chr14:104095160-104095917	H1-hESC	embryonic stem cell:	n/a	n/a
41	EP300	chr14:104094550-104095871	HepG2	liver:	n/a	chr14:104095604-104095620 chr14:104095745-104095761
42	CREB1	chr14:104094986-104096377	A549	lung:	n/a	n/a
43	MXI1	chr14:104094505-104096491	HepG2	liver:	n/a	n/a
44	POLR2A	chr14:104094165-104095938	K562	blood:	n/a	n/a
45	POLR2A	chr14:104094992-104095939	A549	lung:	n/a	n/a
46	YY1	chr14:104094679-104096476	SK-N-SH	brain:	n/a	chr14:104096179-104096193 chr14:104095542-104095564 chr14:104095226-104095237 chr14:104095554-104095568 chr14:104095542-104095552 chr14:104096185-104096194 chr14:104095256-104095270 chr14:104095541-104095553 chr14:104096188-104096197 chr14:104095157-104095168 chr14:104096182-104096196
47	CTCF	chr14:104095180-104095330	GM12867	blood:	n/a	n/a
48	MAFK	chr14:104095282-104095500	HepG2	liver:	n/a	n/a
49	POLR2A	chr14:104094262-104096415	GM19193	blood:	n/a	n/a
50	MYC	chr14:104095210-104095788	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:104040559..104042718-chr14:104094686..104097466,2	K562	blood:
2	chr14:104094610..104096385-chr14:104176505..104178992,4	MCF-7	breast:
3	chr14:104092649..104097026-chr14:104179930..104185119,7	MCF-7	breast:
4	chr14:104092617..104095465-chr14:104143281..104145342,2	MCF-7	breast:
5	chr14:104026845..104031617-chr14:104090112..104098528,12	MCF-7	breast:
6	chr14:104095098..104097162-chr14:104179460..104182190,3	K562	blood:
7	chr14:104093558..104096899-chr14:104170639..104176222,7	MCF-7	breast:
8	chr14:104093419..104097122-chr14:104180603..104183015,4	K562	blood:
9	chr14:104095056..104095737-chr19:6530310..6531125,2	Hela-S3	cervix:
10	chr14:103800320..103802027-chr14:104094175..104096275,2	K562	blood:
11	chr14:104095140..104096884-chr14:104158687..104161252,3	MCF-7	breast:
12	chr14:104091773..104098220-chr14:104179036..104183968,10	MCF-7	breast:
13	chr14:104094844..104097550-chr17:58154950..58156929,2	MCF-7	breast:
14	chr11:10829389..10830011-chr14:104095148..104095969,2	Hela-S3	cervix:
15	chr14:104094584..104096859-chr14:104165203..104168753,3	MCF-7	breast:
16	chr14:104095132..104095741-chr5:172385493..172386243,2	Hela-S3	cervix:
17	chr14:104093531..104096163-chr14:104161716..104165608,3	MCF-7	breast:
18	chr14:103986778..103989691-chr14:104095238..104098302,4	K562	blood:
19	chr14:104092924..104095729-chr14:104175116..104177946,2	K562	blood:
20	chr14:104093231..104097862-chr14:104156769..104161796,10	MCF-7	breast:
21	chr14:104026767..104030601-chr14:104092111..104097061,5	MCF-7	breast:
22	chr14:104038550..104040272-chr14:104093339..104095462,2	MCF-7	breast:
23	chr14:104094629..104095486-chr9:130547796..130548645,2	Hela-S3	cervix:
24	chr14:104094760..104097289-chr14:104157296..104159578,3	K562	blood:
25	chr14:103799673..103801473-chr14:104094141..104096279,2	MCF-7	breast:
26	chr14:104092924..104097008-chr14:104171636..104177946,5	K562	blood:

Variant related genes	Relation type
KLC1	TF binding region
ENSG00000166170	Chromatin interaction
ENSG00000256053	Chromatin interaction
ENSG00000204758	Chromatin interaction
ENSG00000125657	Chromatin interaction
ENSG00000136807	Chromatin interaction
ENSG00000224997	Chromatin interaction
ENSG00000269940	Chromatin interaction
ENSG00000269963	Chromatin interaction
ENSG00000068097	Chromatin interaction
ENSG00000100711	Chromatin interaction
ENSG00000126215	Chromatin interaction
ENSG00000269958	Chromatin interaction
ENSG00000267416	Chromatin interaction
ENSG00000110321	Chromatin interaction
ENSG00000126214	Chromatin interaction
ENSG00000037241	Chromatin interaction
ENSG00000166165	Chromatin interaction
ENSG00000266070	Chromatin interaction
ENSG00000269910	Chromatin interaction
ENSG00000100664	Chromatin interaction
ENSG00000264904	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10459574	0.87[ASN][1000 genomes]
rs11540512	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11844466	0.92[AFR][1000 genomes]
rs11846404	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11846838	0.81[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs11851000	0.91[AFR][1000 genomes]
rs11851616	0.92[AFR][1000 genomes]
rs12147645	0.92[CEU][hapmap];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12590968	0.87[AFR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12888993	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12889403	0.88[CHD][hapmap];0.84[JPT][hapmap];0.91[MEX][hapmap]
rs12889731	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12892038	0.92[AFR][1000 genomes]
rs12896171	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1606	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1799796	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2273175	0.92[CEU][hapmap];0.81[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2295152	0.83[EUR][1000 genomes]
rs2296482	0.88[CHD][hapmap];0.91[MEX][hapmap]
rs2403197	0.82[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.95[MEX][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs3212024	0.83[EUR][1000 genomes]
rs3212038	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs3212076	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3212090	0.87[CEU][hapmap];0.88[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34000399	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34026011	0.88[CHD][hapmap];0.91[MEX][hapmap]
rs34843146	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35011804	0.83[AFR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35921969	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4525427	0.92[AFR][1000 genomes]
rs4900590	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4900591	1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4900592	0.85[EUR][1000 genomes]
rs4906335	0.90[CHD][hapmap];0.91[MEX][hapmap]
rs4906347	0.82[AFR][1000 genomes]
rs4906350	0.98[AFR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4906356	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57072546	0.89[AFR][1000 genomes]
rs60249782	0.89[AFR][1000 genomes]
rs61637848	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7148456	0.88[CHD][hapmap];0.91[MEX][hapmap]
rs7148857	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs729438	0.87[CEU][hapmap];0.88[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.85[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8017993	0.88[CHD][hapmap];0.91[MEX][hapmap]
rs8021229	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers 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 target site	162 gene(s)	inside rSNPs	diseases
2	nsv832883	chr14:103927687-104120953	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv902300	chr14:103967504-104205811	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription 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 target site	83 gene(s)	inside rSNPs	diseases
4	nsv1052010	chr14:104061472-104216267	Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Flanking 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	52 gene(s)	inside rSNPs	diseases
5	nsv542201	chr14:104061472-104216267	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
6	nsv456435	chr14:104061646-104198251	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
7	nsv566023	chr14:104061646-104198251	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
8	esv3490243	chr14:104083248-104099394	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription 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	28 gene(s)	inside rSNPs	diseases
9	esv3490244	chr14:104083248-104099394	Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	28 gene(s)	inside rSNPs	diseases
10	nsv902308	chr14:104087209-104211180	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs12884809	MARK3	cis	cerebellum	SCAN
rs12884809	ZFYVE21	cis	cerebellum	SCAN
rs12884809	RP11-73M18.8	cis	Artery Tibial	GTEx
rs12884809	RP11-73M18.8	cis	Whole Blood	GTEx
rs12884809	RP11-73M18.8	cis	Nerve Tibial	GTEx
rs12884809	ZFYVE21	cis	lymphoblastoid	seeQTL
rs12884809	C14orf153	cis	parietal	SCAN
rs12884809	KLC1	cis	Whole Blood	GTEx
rs12884809	C14orf153	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104094000-104095400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr14:104094200-104095400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:104094200-104095400	Flanking Active TSS	Stomach Smooth Muscle	stomach
4	chr14:104094400-104095400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr14:104094400-104096400	Active TSS	Duodenum Mucosa	Duodenum
6	chr14:104094400-104096800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:104094400-104096800	Active TSS	Fetal Brain Female	brain
8	chr14:104094400-104097200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr14:104094400-104097200	Active TSS	Psoas Muscle	Psoas
10	chr14:104094400-104097400	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr14:104094400-104097600	Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr14:104094600-104096600	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr14:104094600-104096600	Active TSS	Gastric	stomach
14	chr14:104094600-104096600	Active TSS	Left Ventricle	heart
15	chr14:104094600-104096800	Active TSS	H9 Cell Line	embryonic stem cell
16	chr14:104094600-104096800	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr14:104094600-104096800	Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr14:104094600-104096800	Active TSS	Brain Substantia Nigra	brain
19	chr14:104094600-104096800	Active TSS	HepG2	liver
20	chr14:104094600-104097000	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr14:104094600-104097200	Active TSS	Ovary	ovary
22	chr14:104094600-104097200	Active TSS	Right Atrium	heart
23	chr14:104094600-104097400	Active TSS	Aorta	Aorta
24	chr14:104094600-104097400	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr14:104094800-104095400	Flanking Active TSS	NH-A	brain
26	chr14:104094800-104096000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
27	chr14:104094800-104096400	Active TSS	Fetal Kidney	kidney
28	chr14:104094800-104096400	Active TSS	Small Intestine	intestine
29	chr14:104094800-104096600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:104094800-104096600	Active TSS	Esophagus	oesophagus
31	chr14:104094800-104096800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr14:104094800-104096800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr14:104094800-104096800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr14:104094800-104096800	Active TSS	Brain Anterior Caudate	brain
35	chr14:104094800-104096800	Active TSS	Brain Hippocampus Middle	brain
36	chr14:104094800-104096800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr14:104094800-104096800	Active TSS	GM12878-XiMat	blood
38	chr14:104094800-104097000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr14:104094800-104097000	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr14:104094800-104097200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr14:104094800-104097400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr14:104095000-104095400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:104095000-104095600	Active TSS	Brain Germinal Matrix	brain
44	chr14:104095000-104096200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr14:104095000-104096400	Active TSS	Primary monocytes fromperipheralblood	blood
46	chr14:104095000-104096400	Active TSS	Primary T cells from cord blood	blood
47	chr14:104095000-104096400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr14:104095000-104096400	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr14:104095000-104096400	Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr14:104095000-104096400	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood

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