Variant report

Variant	rs3754211
Chromosome Location	chr1:150951857-150951858
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	EP300	chr1:150951735-150952365	A549	lung:	n/a	n/a
2	CTCF	chr1:150951621-150952472	H1-hESC	embryonic stem cell:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
3	YY1	chr1:150951852-150952294	HepG2	liver:	n/a	chr1:150952157-150952167 chr1:150952157-150952179 chr1:150952160-150952168
4	CTCF	chr1:150951395-150952611	HCT-116	colon:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
5	FOXA1	chr1:150951728-150952170	HepG2	liver:	n/a	n/a
6	CTCF	chr1:150951706-150952519	A549	lung:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
7	RUNX3	chr1:150951744-150952268	GM12878	blood:	n/a	n/a
8	CTCF	chr1:150951587-150952454	K562	blood:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
9	CTCF	chr1:150951775-150951867	GM12878	blood:	n/a	n/a
10	TCF12	chr1:150951664-150952470	A549	lung:	n/a	chr1:150951726-150951734
11	FOXA2	chr1:150951539-150952206	HepG2	liver:	n/a	n/a
12	RAD21	chr1:150951838-150952400	H1-hESC	embryonic stem cell:	n/a	chr1:150952149-150952158 chr1:150952143-150952162 chr1:150952111-150952130
13	NFIC	chr1:150951846-150952448	SK-N-SH	brain:	n/a	n/a
14	MAX	chr1:150951432-150952214	K562	blood:	n/a	chr1:150951680-150951690
15	ZBTB7A	chr1:150951831-150952287	ECC-1	luminal epithelium:	n/a	n/a
16	HDAC2	chr1:150951833-150952340	HepG2	liver:	n/a	n/a
17	YY1	chr1:150951848-150952262	H1-hESC	embryonic stem cell:	n/a	chr1:150952157-150952167 chr1:150952157-150952179 chr1:150952160-150952168
18	ZC3H11A	chr1:150951690-150952258	K562	blood:	n/a	n/a
19	CTCF	chr1:150951624-150952580	K562	blood:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
20	PAX5	chr1:150951845-150952228	GM12878	blood:	n/a	n/a
21	PML	chr1:150951852-150952431	GM12878	blood:	n/a	n/a
22	RAD21	chr1:150951702-150952558	SK-N-SH	brain:	n/a	chr1:150952149-150952158 chr1:150952143-150952162 chr1:150952111-150952130
23	RFX5	chr1:150951824-150952353	HepG2	liver:	n/a	n/a
24	CTCF	chr1:150951639-150952338	HepG2	liver:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
25	MYBL2	chr1:150951790-150952421	HepG2	liver:	n/a	n/a
26	RAD21	chr1:150951836-150952376	H1-hESC	embryonic stem cell:	n/a	chr1:150952149-150952158 chr1:150952143-150952162 chr1:150952111-150952130
27	CTCF	chr1:150951797-150952432	A549	lung:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
28	CTCF	chr1:150951597-150952310	H1-hESC	embryonic stem cell:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
29	MAX	chr1:150951516-150952340	NB4	blood:	n/a	chr1:150951680-150951690
30	CTCF	chr1:150951746-150951893	GM19238	blood:	n/a	n/a
31	CTCF	chr1:150951840-150952302	Lung_OC	lung:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
32	MYC	chr1:150951545-150952311	NB4	blood:	n/a	chr1:150951680-150951690
33	CTCF	chr1:150951532-150952641	HCT-116	colon:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
34	RAD21	chr1:150951808-150952469	MCF-7	breast:	n/a	chr1:150952149-150952158 chr1:150952143-150952162 chr1:150952111-150952130
35	CTCF	chr1:150951757-150952344	T-47D	breast:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
36	ATF2	chr1:150951834-150952294	H1-hESC	embryonic stem cell:	n/a	n/a
37	NFIC	chr1:150951850-150952428	ECC-1	luminal epithelium:	n/a	n/a
38	BACH1	chr1:150951830-150952302	H1-hESC	embryonic stem cell:	n/a	n/a
39	FOXA1	chr1:150951624-150952141	HepG2	liver:	n/a	n/a
40	RUNX3	chr1:150951751-150952338	GM12878	blood:	n/a	n/a
41	CTCF	chr1:150951789-150952287	GM19240	blood:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
42	CTCF	chr1:150951531-150952540	K562	blood:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
43	CTCF	chr1:150951358-150952694	MCF-7	breast:	n/a	chr1:150952113-150952122 chr1:150952110-150952128 chr1:150952146-150952162 chr1:150952145-150952163 chr1:150952113-150952126 chr1:150952140-150952161 chr1:150952112-150952133
44	CTCF	chr1:150951807-150951955	Kidney_OC	kidney:	n/a	n/a
45	POLR2A	chr1:150951852-150952154	HepG2	liver:	n/a	n/a
46	FOXA1	chr1:150951620-150952030	T-47D	breast:	n/a	n/a
47	HMGN3	chr1:150951841-150952078	K562	blood:	n/a	n/a
48	MAZ	chr1:150951786-150952500	IMR90	lung:	n/a	n/a
49	ATF3	chr1:150951838-150952374	HepG2	liver:	n/a	chr1:150951938-150951951
50	MAX	chr1:150951840-150952395	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:150950114..150952556-chr1:150975284..150977893,2	K562	blood:
2	chr1:150951645..150956254-chr1:150963775..150970753,11	MCF-7	breast:
3	chr1:150951592..150952599-chr1:150967788..150968979,9	K562	blood:
4	chr1:150951726..150952264-chr1:150978956..150979621,3	MCF-7	breast:
5	chr1:150951698..150952219-chr2:98281076..98281596,2	MCF-7	breast:
6	chr1:150848210..150848854-chr1:150951690..150952505,2	K562	blood:
7	chr1:150898177..150900338-chr1:150951575..150953593,2	MCF-7	breast:
8	chr1:150950305..150952431-chr1:150971107..150975123,3	K562	blood:
9	chr1:150533509..150537383-chr1:150951108..150953934,3	K562	blood:
10	chr1:150897410..150900366-chr1:150947492..150952156,4	K562	blood:
11	chr1:150951620..150955085-chr1:150979651..150983018,4	K562	blood:
12	chr1:150951690..150952619-chr5:171180404..171181145,2	MCF-7	breast:
13	chr1:150950614..150952256-chr1:151042194..151044224,2	MCF-7	breast:
14	chr1:150951084..150953153-chr1:150955362..150957239,2	K562	blood:
15	chr1:150950100..150952046-chr1:150977560..150979538,2	MCF-7	breast:
16	chr1:150457058..150457964-chr1:150951784..150952748,2	K562	blood:
17	chr1:150951614..150952389-chr1:151128181..151129185,3	K562	blood:
18	chr1:150951711..150952336-chr17:59627467..59628156,2	MCF-7	breast:
19	chr1:150951680..150952626-chr1:150978638..150980238,11	MCF-7	breast:
20	chr1:150931619..150932303-chr1:150951721..150952541,2	K562	blood:
21	chr1:150951712..150952263-chr1:201481819..201482668,2	MCF-7	breast:
22	chr1:150943416..150944134-chr1:150951754..150952614,4	MCF-7	breast:
23	chr1:150533163..150533947-chr1:150951810..150952543,2	MCF-7	breast:
24	chr1:150950075..150953840-chr1:150979246..150981801,5	K562	blood:
25	chr1:150951796..150952519-chr20:53263209..53263715,2	MCF-7	breast:
26	chr1:150951698..150952590-chr1:151043181..151044003,3	K562	blood:
27	chr1:150940313..150941336-chr1:150951606..150952463,3	MCF-7	breast:
28	chr1:150950114..150953759-chr1:150976393..150978885,3	K562	blood:
29	chr1:150951734..150952504-chr17:55320266..55320869,2	MCF-7	breast:
30	chr1:150951720..150952259-chr5:171542423..171542944,2	MCF-7	breast:
31	chr1:150929171..150929726-chr1:150951821..150952601,2	MCF-7	breast:
32	chr1:150950574..150954547-chr1:151027400..151032185,6	MCF-7	breast:
33	chr1:150835862..150838203-chr1:150950221..150953041,2	K562	blood:
34	chr1:150951645..150952602-chr1:150985713..150986225,2	K562	blood:
35	chr1:150951736..150952574-chr1:150978895..150979837,4	K562	blood:
36	chr1:150748050..150749658-chr1:150951794..150953371,2	K562	blood:
37	chr1:150951440..150951966-chr1:150980502..150981090,2	MCF-7	breast:
38	chr1:150951497..150952389-chr3:63729971..63730474,2	MCF-7	breast:
39	chr1:150934059..150935054-chr1:150951631..150952393,3	MCF-7	breast:
40	chr1:150950155..150952613-chr1:151029273..151031994,2	MCF-7	breast:
41	chr1:150928686..150929491-chr1:150951648..150952588,2	K562	blood:
42	chr1:150951678..150952589-chr1:150967817..150969035,6	MCF-7	breast:
43	chr1:150951724..150952441-chr1:150967105..150967608,2	MCF-7	breast:
44	chr1:150898744..150899296-chr1:150951619..150952226,2	K562	blood:
45	chr1:150897987..150899186-chr1:150951760..150952511,3	MCF-7	breast:

Variant related genes	Relation type
CERS2	TF binding region
ANXA9	TF binding region
ENSG00000143379	Chromatin interaction
ENSG00000163156	Chromatin interaction
ENSG00000143409	Chromatin interaction
ENSG00000201806	Chromatin interaction
ENSG00000143418	Chromatin interaction
ENSG00000213190	Chromatin interaction
ENSG00000143458	Chromatin interaction
ENSG00000143363	Chromatin interaction
ENSG00000197622	Chromatin interaction
ENSG00000163154	Chromatin interaction
ENSG00000203804	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 35 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1081512	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11204735	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs11204737	1.00[CEU][hapmap];0.95[TSI][hapmap];0.83[EUR][1000 genomes]
rs11204749	0.84[YRI][hapmap]
rs11204752	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11204754	0.92[YRI][hapmap]
rs11587718	0.90[CHB][hapmap];0.87[ASN][1000 genomes]
rs11587720	0.89[ASN][1000 genomes]
rs12125650	1.00[CEU][hapmap];0.95[TSI][hapmap]
rs12126004	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12402006	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12404199	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12410050	0.87[EUR][1000 genomes]
rs12758227	0.84[EUR][1000 genomes]
rs1673160	0.85[CHB][hapmap];0.87[ASN][1000 genomes]
rs2089081	0.80[EUR][1000 genomes]
rs2280627	0.81[YRI][hapmap]
rs2305814	0.85[CHB][hapmap];0.98[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];0.86[MEX][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs267735	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs486836	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4970932	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6587551	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7412746	0.84[EUR][1000 genomes]
rs752376	0.83[MEX][hapmap]
rs7532008	0.85[CHB][hapmap];0.98[CHD][hapmap]
rs771201	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001897	chr1:150743271-151241600	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv535158	chr1:150743271-151241600	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv1008496	chr1:150845827-150970656	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
4	nsv522317	chr1:150933723-150974162	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv522840	chr1:150933723-151347746	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	169 gene(s)	inside rSNPs	diseases

mRNA abundance (count:35)

SNP	Gene	Cis/trans	Tissue	Source
rs3754211	RP11-316M1.12	cis	Esophagus Muscularis	GTEx
rs3754211	HORMAD1	cis	parietal	SCAN
rs3754211	CTSK	cis	lymphoblastoid	seeQTL
rs3754211	RP11-316M1.12	cis	Nerve Tibial	GTEx
rs3754211	RP11-316M1.12	cis	Adipose Subcutaneous	GTEx
rs3754211	ARNT	cis	multi-tissue	Pritchard
rs3754211	CTSK	Cis_1M	lymphoblastoid	RTeQTL
rs3754211	PSMD4	cis	parietal	SCAN
rs3754211	MCL1	cis	cerebellum	SCAN
rs3754211	HORMAD1	cis	lesional skin	skin_eQTL
rs3754211	CTSS	cis	cerebellum	SCAN
rs3754211	CTSK	cis	cerebellum	SCAN
rs3754211	RP11-316M1.12	cis	Skin Sun Exposed Lower leg	GTEx
rs3754211	RNU6-1042P	cis	Esophagus Mucosa	GTEx
rs3754211	ARNT	cis	normal skin	skin_eQTL
rs3754211	HORMAD1	cis	Esophagus Mucosa	GTEx
rs3754211	ARNT	cis	uninvolved skin	skin_eQTL
rs3754211	RP11-316M1.12	cis	Muscle Skeletal	GTEx
rs3754211	RP11-316M1.12	cis	Artery Tibial	GTEx
rs3754211	FLG	cis	cerebellum	SCAN
rs3754211	HORMAD1	cis	uninvolved skin	skin_eQTL
rs3754211	CTSK	cis	multi-tissue	Pritchard
rs3754211	RP11-316M1.12	cis	Thyroid	GTEx
rs3754211	RP11-316M1.12	cis	lung	GTEx
rs3754211	HORMAD1	cis	Skin Sun Exposed Lower leg	GTEx
rs3754211	CTSS	cis	parietal	SCAN
rs3754211	RP11-316M1.12	cis	Whole Blood	GTEx
rs3754211	CTSS	Cis_1M	lymphoblastoid	RTeQTL
rs3754211	ARNT	cis	cerebellum	SCAN
rs3754211	CTSS	cis	lymphoblastoid	seeQTL
rs3754211	CTSK	cis	parietal	SCAN
rs3754211	ARNT	Cis_1M	lymphoblastoid	RTeQTL
rs3754211	ARNT	cis	parietal	SCAN
rs3754211	HORMAD1	cis	Nerve Tibial	GTEx
rs3754211	FMO5	cis	cerebellum	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150948000-150952600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:150948000-150952600	Enhancers	Fetal Intestine Small	intestine
3	chr1:150948200-150952000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:150948600-150952800	Enhancers	Placenta	Placenta
5	chr1:150948800-150952000	Enhancers	Lung	lung
6	chr1:150949200-150952600	Enhancers	NH-A	brain
7	chr1:150950200-150952800	Enhancers	HMEC	breast
8	chr1:150950200-150953400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr1:150950200-150953400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:150950200-150953600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:150950200-150953600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:150950200-150953600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:150950200-150953800	Weak transcription	Right Ventricle	heart
14	chr1:150950200-150954200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr1:150950400-150952600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:150950400-150953400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:150950400-150953600	Weak transcription	HSMMtube	muscle
18	chr1:150950600-150952800	Enhancers	Hela-S3	cervix
19	chr1:150950800-150952200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr1:150951000-150952600	Enhancers	Fetal Muscle Leg	muscle
21	chr1:150951200-150953800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:150951400-150952000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr1:150951400-150952000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:150951400-150952000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:150951400-150952200	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr1:150951400-150952200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:150951400-150952200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr1:150951400-150952400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:150951400-150952400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr1:150951400-150952400	Flanking Active TSS	HepG2	liver
31	chr1:150951400-150952400	Flanking Active TSS	K562	blood
32	chr1:150951400-150952600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr1:150951400-150952600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:150951400-150952600	Enhancers	Stomach Mucosa	stomach
35	chr1:150951400-150952800	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr1:150951600-150952000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr1:150951600-150952000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:150951600-150952000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:150951600-150952000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:150951600-150952000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr1:150951600-150952000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr1:150951600-150952000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:150951600-150952000	Flanking Active TSS	Primary T cells from cord blood	blood
44	chr1:150951600-150952000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
45	chr1:150951600-150952000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr1:150951600-150952000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr1:150951600-150952000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr1:150951600-150952000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr1:150951600-150952000	Flanking Active TSS	Colon Smooth Muscle	Colon
50	chr1:150951600-150952000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum

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