Variant report

Variant	rs74115707
Chromosome Location	chr1:153722019-153722020
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	JUND	chr1:153721896-153722223	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr1:153721899-153722307	HepG2	liver:	n/a	chr1:153722139-153722152
3	MYC	chr1:153721972-153722198	MCF-7	breast:	n/a	chr1:153722140-153722151
4	MAX	chr1:153721896-153722275	Hela-S3	cervix:	n/a	chr1:153722140-153722151
5	CTCF	chr1:153721918-153722224	A549	lung:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
6	CTCF	chr1:153721747-153722322	MCF-7	breast:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
7	CTCF	chr1:153721940-153722090	AG04450	lung:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
8	CTCF	chr1:153721920-153722220	GM12891	blood:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
9	FOS	chr1:153721961-153722158	MCF10A-Er-Src	breast:	n/a	n/a
10	RAD21	chr1:153721797-153722319	ECC-1	luminal epithelium:	n/a	chr1:153722058-153722077
11	SPI1	chr1:153721906-153722252	GM12878	blood:	n/a	n/a
12	CTCF	chr1:153722000-153722150	GM12878	blood:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
13	CTCF	chr1:153722000-153722150	HPAF	blood vessel:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
14	CEBPB	chr1:153721846-153722208	A549	lung:	n/a	n/a
15	MXI1	chr1:153721903-153722246	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:153721917-153722224	Gliobla	brain:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
17	RAD21	chr1:153721879-153722222	K562	blood:	n/a	chr1:153722058-153722077
18	MYC	chr1:153721923-153722203	MCF10A-Er-Src	breast:	n/a	chr1:153722140-153722151
19	RAD21	chr1:153721811-153722292	ECC-1	luminal epithelium:	n/a	chr1:153722058-153722077
20	CTCF	chr1:153721860-153722219	ECC-1	luminal epithelium:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
21	CTCF	chr1:153722000-153722150	AG09319	gingival:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
22	RAD21	chr1:153721684-153722397	A549	lung:	n/a	chr1:153722058-153722077
23	CTCF	chr1:153721863-153722279	K562	blood:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
24	CTCF	chr1:153721891-153722186	A549	lung:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
25	EP300	chr1:153721962-153722209	K562	blood:	n/a	chr1:153722180-153722194
26	CTCF	chr1:153721960-153722110	HCT-116	colon:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
27	RAD21	chr1:153721827-153722273	IMR90	lung:	n/a	chr1:153722058-153722077
28	RAD21	chr1:153721878-153722263	A549	lung:	n/a	chr1:153722058-153722077
29	RAD21	chr1:153721806-153722272	HepG2	liver:	n/a	chr1:153722058-153722077
30	STAT1	chr1:153721936-153722227	GM12878	blood:	n/a	n/a
31	CTCF	chr1:153722000-153722150	AG10803	skin:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
32	BATF	chr1:153721944-153722245	GM12878	blood:	n/a	n/a
33	SPI1	chr1:153721957-153722280	GM12891	blood:	n/a	n/a
34	SMC3	chr1:153721657-153722468	SK-N-SH	brain:	n/a	chr1:153722062-153722076
35	BHLHE40	chr1:153721885-153723522	K562	blood:	n/a	chr1:153722139-153722152
36	CTCF	chr1:153722000-153722150	AG04449	skin:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
37	YY1	chr1:153721892-153722200	GM12891	blood:	n/a	n/a
38	CTCF	chr1:153721938-153722189	GM20000	blood:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
39	CTCF	chr1:153721782-153722383	MCF-7	breast:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
40	SMC3	chr1:153721800-153722327	Hela-S3	cervix:	n/a	chr1:153722062-153722076
41	CTCF	chr1:153721920-153722178	A549	lung:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
42	CHD2	chr1:153721914-153722212	Hela-S3	cervix:	n/a	n/a
43	ZNF143	chr1:153721895-153722240	K562	blood:	n/a	n/a
44	MYC	chr1:153721951-153722284	K562	blood:	n/a	chr1:153722140-153722151
45	CTCF	chr1:153721940-153722090	RPTEC	kidney:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
46	CTCF	chr1:153722000-153722150	Caco-2	colon:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
47	FOXM1	chr1:153721841-153722283	GM12878	blood:	n/a	n/a
48	CEBPB	chr1:153721841-153722197	HepG2	liver:	n/a	n/a
49	CTCF	chr1:153721933-153722221	HUVEC	blood vessel:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077
50	CTCF	chr1:153721980-153722130	Hela-S3	cervix:	n/a	chr1:153722067-153722074 chr1:153722060-153722078 chr1:153722055-153722076 chr1:153722061-153722077

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153721986-153722036	HCM	heart:	n/a
2	chr1:153721986-153722036	MCF10A-Er-Src	breast:	n/a
3	chr1:153721986-153722036	AG09319	gingival:	n/a
4	chr1:153721986-153722036	GM12892	blood:	n/a
5	chr1:153721986-153722036	NHBE	bronchial:	n/a
6	chr1:153721986-153722036	A549	lung:	n/a
7	chr1:153721986-153722036	NHDF-neo	bronchial:	n/a
8	chr1:153721986-153722036	SK-N-MC	brain:	n/a
9	chr1:153721986-153722036	GM19239	blood:	n/a
10	chr1:153721986-153722036	SK-N-SH_RA	brain:	n/a
11	chr1:153721986-153722036	HRE	kidney:	n/a
12	chr1:153721986-153722036	HCT-116	colon:	n/a
13	chr1:153721986-153722036	HCPEpiC	choroid plexus:	n/a
14	chr1:153721986-153722036	NT2-D1	testis:	n/a
15	chr1:153721986-153722036	PrEC	prostate:	n/a
16	chr1:153721986-153722036	AG10803	skin:	n/a
17	chr1:153721986-153722036	HCF	heart:	n/a
18	chr1:153721986-153722036	K562	blood:	n/a
19	chr1:153721986-153722036	HRPEpiC	eye:	n/a
20	chr1:153721986-153722036	H1-hESC	embryonic stem cell:	embryo
21	chr1:153721986-153722036	HL-60	blood:	n/a
22	chr1:153721986-153722036	HIPEpiC	eye:	n/a
23	chr1:153721986-153722036	ProgFib	skin:	n/a
24	chr1:153721986-153722036	NB4	blood:	n/a
25	chr1:153721986-153722036	AG09309	skin:	n/a
26	chr1:153721986-153722036	HepG2	liver:	n/a
27	chr1:153721986-153722036	ovcar-3	ovarian:	n/a
28	chr1:153721986-153722036	HEK293	kidney:	embryo
29	chr1:153721986-153722036	IMR90	lung:	fetal
30	chr1:153721986-153722036	RPTEC	kidney:	n/a
31	chr1:153721986-153722036	T-47D	breast:	n/a
32	chr1:153721986-153722036	HUVEC	blood vessel:	n/a
33	chr1:153721986-153722036	AoSMC	blood vessel:	n/a
34	chr1:153721986-153722036	ECC-1	luminal epithelium:	n/a
35	chr1:153721986-153722036	BE2_C	brain:	n/a
36	chr1:153721986-153722036	AG04450	lung:	fetal
37	chr1:153721986-153722036	PANC-1	pancreas:	n/a
38	chr1:153721986-153722036	BJ	skin:	n/a
39	chr1:153721986-153722036	Hela-S3	cervix:	n/a
40	chr1:153721986-153722036	MCF-7	breast:	n/a
41	chr1:153721986-153722036	HNPCEpiC	eye:	n/a
42	chr1:153721986-153722036	AG04449	skin:	fetal
43	chr1:153721986-153722036	SAEC	small airway:	n/a
44	chr1:153721986-153722036	SK-N-SH	brain:	n/a
45	chr1:153721986-153722036	HRCEpiC	kidney:	n/a
46	chr1:153721986-153722036	PFSK-1	brain:	n/a
47	chr1:153721986-153722036	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:153721986-153722036	LNCaP	prostate:	n/a
49	chr1:153721986-153722036	HMEC	breast:	n/a
50	chr1:153721986-153722036	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:153649801..153651197-chr1:153721624..153722795,7	K562	blood:
2	chr1:153720991..153724810-chr1:153725795..153729552,4	K562	blood:
3	chr1:153649948..153651441-chr1:153721197..153722962,13	MCF-7	breast:
4	chr1:153718689..153722494-chr1:153754565..153757255,3	MCF-7	breast:
5	chr1:153721609..153722201-chr1:153958885..153959530,2	MCF-7	breast:
6	chr1:153720153..153722132-chr1:153938351..153940941,2	K562	blood:
7	chr1:153649696..153652136-chr1:153718198..153722635,6	MCF-7	breast:
8	chr1:153641918..153644104-chr1:153718831..153722451,3	MCF-7	breast:
9	chr1:153649841..153650855-chr1:153721578..153722543,22	MCF-7	breast:
10	chr1:153325553..153326297-chr1:153721614..153722133,2	MCF-7	breast:
11	chr1:153483193..153484052-chr1:153721737..153722436,2	MCF-7	breast:
12	chr1:153619135..153622133-chr1:153720546..153722065,2	K562	blood:
13	chr1:153719991..153722380-chr1:153747538..153749558,2	K562	blood:
14	chr1:153604435..153608010-chr1:153720589..153722961,3	MCF-7	breast:
15	chr1:153481978..153482877-chr1:153721728..153722487,3	K562	blood:
16	chr1:153720924..153726415-chr1:153745287..153750957,9	MCF-7	breast:
17	chr1:153707078..153709228-chr1:153718414..153722643,3	MCF-7	breast:
18	chr1:153601040..153604537-chr1:153718761..153722093,3	K562	blood:
19	chr1:153721868..153723667-chr1:153746625..153749637,3	MCF-7	breast:
20	chr1:153544752..153545630-chr1:153721678..153722583,3	MCF-7	breast:
21	chr1:153588561..153590573-chr1:153720516..153722822,2	K562	blood:
22	chr1:153698814..153704322-chr1:153719587..153724035,6	MCF-7	breast:
23	chr1:153721928..153724175-chr1:153731100..153734049,2	MCF-7	breast:

Variant related genes	Relation type
INTS3	TF binding region
INTS3	CpG island
ENSG00000143554	Chromatin interaction
ENSG00000189171	Chromatin interaction
ENSG00000271853	Chromatin interaction
ENSG00000199565	Chromatin interaction
ENSG00000143570	Chromatin interaction
ENSG00000189334	Chromatin interaction
ENSG00000143621	Chromatin interaction
ENSG00000160679	Chromatin interaction
ENSG00000143624	Chromatin interaction
ENSG00000143578	Chromatin interaction
ENSG00000272030	Chromatin interaction
ENSG00000169418	Chromatin interaction
ENSG00000238511	Chromatin interaction
ENSG00000273026	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs16835535	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16835548	0.87[AFR][1000 genomes];1.00[AMR][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	esv2830411	chr1:153613393-153725007	Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Active TSS Weak transcription 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	48 gene(s)	inside rSNPs	diseases
2	nsv1067771	chr1:153613593-153724866	Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Enhancers Active TSS 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 miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv530052	chr1:153613593-153724866	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	nsv1005818	chr1:153613597-153724980	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	nsv535173	chr1:153613597-153724980	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	nsv1007835	chr1:153613597-153729959	Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Active 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	48 gene(s)	inside rSNPs	diseases
7	nsv535174	chr1:153613597-153729959	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
8	nsv1011897	chr1:153613597-153836703	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats 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	70 gene(s)	inside rSNPs	diseases
9	nsv464028	chr1:153622220-153723037	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	nsv547929	chr1:153622220-153723037	Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	nsv999364	chr1:153622634-154419436	Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
12	nsv535175	chr1:153622634-154419436	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	286 gene(s)	inside rSNPs	diseases
13	nsv1001312	chr1:153622834-153724867	Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv535176	chr1:153622834-153724867	Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv531892	chr1:153671910-153954090	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
16	nsv464039	chr1:153708906-153801098	Genic enhancers Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
17	nsv547941	chr1:153708906-153801098	Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers Bivalent Enhancer 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 miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153707200-153730400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:153707600-153722200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:153711400-153735600	Strong transcription	Fetal Muscle Leg	muscle
4	chr1:153712600-153722400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:153712600-153741400	Strong transcription	Placenta	Placenta
6	chr1:153712800-153725600	Strong transcription	Fetal Lung	lung
7	chr1:153712800-153737800	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr1:153712800-153737800	Strong transcription	Placenta Amnion	Placenta Amnion
9	chr1:153712800-153738000	Strong transcription	Fetal Brain Female	brain
10	chr1:153712800-153738200	Strong transcription	Thymus	Thymus
11	chr1:153712800-153742800	Strong transcription	Fetal Muscle Trunk	muscle
12	chr1:153712800-153743200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr1:153712800-153744800	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:153712800-153746400	Strong transcription	Brain Germinal Matrix	brain
15	chr1:153712800-153751800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:153713000-153725600	Strong transcription	Primary hematopoietic stem cells	blood
17	chr1:153713000-153728600	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:153713000-153734800	Strong transcription	Spleen	Spleen
19	chr1:153713000-153735200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:153713000-153738200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:153713000-153738600	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr1:153713000-153745400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr1:153713000-153745400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr1:153713000-153746400	Strong transcription	Primary T cells from cord blood	blood
25	chr1:153713000-153747000	Strong transcription	Dnd41	blood
26	chr1:153714000-153746800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:153715200-153738000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:153715400-153723000	Weak transcription	Right Atrium	heart
29	chr1:153715400-153724600	Strong transcription	NH-A	brain
30	chr1:153715400-153724800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:153715400-153745600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:153715600-153725600	Strong transcription	NHEK	skin
33	chr1:153715600-153727600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:153715600-153745600	Strong transcription	Fetal Thymus	thymus
35	chr1:153715800-153724400	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr1:153715800-153728400	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr1:153716000-153722200	Strong transcription	Fetal Intestine Large	intestine
38	chr1:153716000-153722200	Strong transcription	Fetal Intestine Small	intestine
39	chr1:153716400-153722600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr1:153716400-153723200	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr1:153716400-153723200	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr1:153716400-153746000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr1:153717000-153723400	Strong transcription	GM12878-XiMat	blood
44	chr1:153717200-153722400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr1:153718400-153727800	Strong transcription	Primary B cells from cord blood	blood
46	chr1:153718800-153724400	Strong transcription	NHLF	lung
47	chr1:153718800-153730000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:153719200-153722600	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr1:153719200-153723000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr1:153719400-153725000	Strong transcription	Fetal Brain Male	brain

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