Variant report

Variant	rs10133539
Chromosome Location	chr14:21736596-21736597
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MBD4	chr14:21736436-21738477	HepG2	liver:	n/a	n/a
2	POLR2A	chr14:21736266-21736828	GM12892	blood:	n/a	n/a
3	TEAD4	chr14:21736198-21738533	HepG2	liver:	n/a	n/a
4	POLR2A	chr14:21736592-21736618	K562	blood:	n/a	n/a
5	MYC	chr14:21736535-21738520	NB4	blood:	n/a	chr14:21736997-21737006
6	MYBL2	chr14:21735757-21738673	HepG2	liver:	n/a	chr14:21737687-21737701
7	TBL1XR1	chr14:21736493-21738461	GM12878	blood:	n/a	n/a
8	POLR2A	chr14:21735369-21736757	HUVEC	blood vessel:	n/a	n/a
9	MXI1	chr14:21736372-21738472	Hela-S3	cervix:	n/a	n/a
10	CHD1	chr14:21734912-21738567	IMR90	lung:	n/a	n/a
11	BRCA1	chr14:21736455-21737204	Hela-S3	cervix:	n/a	n/a
12	NFIC	chr14:21736240-21738284	HepG2	liver:	n/a	n/a
13	MYC	chr14:21736316-21738428	K562	blood:	n/a	chr14:21736997-21737006
14	REST	chr14:21736324-21738570	H1-neurons	neurons:	n/a	n/a
15	POLR2A	chr14:21735381-21738234	GM12878	blood:	n/a	n/a
16	CUX1	chr14:21735661-21736646	GM12878	blood:	n/a	n/a
17	POLR2A	chr14:21735190-21738569	GM12891	blood:	n/a	n/a
18	POLR2A	chr14:21735413-21738447	Hela-S3	cervix:	n/a	n/a
19	STAT3	chr14:21736339-21736971	MCF10A-Er-Src	breast:	n/a	chr14:21736686-21736694
20	POLR2A	chr14:21736359-21736789	Hela-S3	cervix:	n/a	n/a
21	MAX	chr14:21736358-21738623	A549	lung:	n/a	chr14:21736997-21737006
22	POLR2A	chr14:21735370-21738563	GM12878	blood:	n/a	n/a
23	E2F4	chr14:21736479-21736710	MCF10A-Er-Src	breast:	n/a	n/a
24	MYC	chr14:21736413-21738430	MCF10A-Er-Src	breast:	n/a	chr14:21736997-21737006
25	MAX	chr14:21736503-21738464	Hela-S3	cervix:	n/a	chr14:21736997-21737006
26	POLR2A	chr14:21735761-21738261	IMR90	lung:	n/a	n/a
27	MYC	chr14:21736476-21738443	K562	blood:	n/a	chr14:21736997-21737006
28	POLR2A	chr14:21735622-21738337	MCF10A-Er-Src	breast:	n/a	n/a
29	NFIC	chr14:21735252-21738638	GM12878	blood:	n/a	n/a
30	POLR2A	chr14:21736556-21736800	GM12891	blood:	n/a	n/a
31	POLR2A	chr14:21736298-21738760	SK-N-MC	brain:	n/a	n/a
32	FOS	chr14:21736401-21736754	MCF10A-Er-Src	breast:	n/a	n/a
33	PML	chr14:21736507-21738634	GM12878	blood:	n/a	chr14:21737514-21737522
34	POLR2A	chr14:21736217-21738412	Hela-S3	cervix:	n/a	n/a
35	MBD4	chr14:21736438-21737808	HepG2	liver:	n/a	n/a
36	POLR2A	chr14:21736383-21736828	GM12891	blood:	n/a	n/a
37	POLR2A	chr14:21736423-21738550	GM12892	blood:	n/a	n/a
38	POLR2A	chr14:21735520-21737795	GM12891	blood:	n/a	n/a
39	POLR2A	chr14:21735285-21738416	MCF10A-Er-Src	breast:	n/a	n/a
40	TAF7	chr14:21736255-21736695	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr14:21736446-21738418	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr14:21736562-21737756	K562	blood:	n/a	n/a
43	POLR2A	chr14:21731378-21738564	GM12878	blood:	n/a	n/a
44	EP300	chr14:21736269-21737077	K562	blood:	n/a	chr14:21736876-21736885
45	POLR2A	chr14:21735239-21737808	HepG2	liver:	n/a	n/a
46	FOS	chr14:21736429-21736697	MCF10A-Er-Src	breast:	n/a	n/a
47	SIN3A	chr14:21735535-21738006	H1-hESC	embryonic stem cell:	n/a	chr14:21737984-21737995
48	POLR2A	chr14:21736485-21738541	GM19193	blood:	n/a	n/a
49	POLR2A	chr14:21728578-21737722	K562	blood:	n/a	n/a
50	SIN3AK20	chr14:21735442-21738552	MCF-7	breast:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21731892..21738562-chr14:21850801..21854193,10	MCF-7	breast:
2	chr14:21678499..21681454-chr14:21736107..21737906,2	MCF-7	breast:
3	chr14:21736434..21738367-chr14:21826392..21828107,2	MCF-7	breast:
4	chr14:21736080..21739636-chr14:21765775..21769584,7	MCF-7	breast:
5	chr14:21734081..21737638-chr14:21753111..21756446,3	K562	blood:
6	chr1:151429381..151432201-chr14:21736244..21738881,2	MCF-7	breast:
7	chr14:21732396..21736856-chr14:21795995..21798414,4	K562	blood:
8	chr14:21698033..21699942-chr14:21736432..21738329,2	MCF-7	breast:
9	chr14:21736489..21738626-chr14:21851688..21853909,3	K562	blood:
10	chr14:21736096..21738321-chr14:38062641..38065635,3	MCF-7	breast:
11	chr14:21735788..21737662-chr17:57969823..57971989,2	MCF-7	breast:

No data

Variant related genes	Relation type
HNRNPC	TF binding region
ENSG00000139865	Chromatin interaction
ENSG00000092200	Chromatin interaction
ENSG00000092201	Chromatin interaction
ENSG00000260830	Chromatin interaction
ENSG00000143442	Chromatin interaction
ENSG00000108443	Chromatin interaction
ENSG00000092199	Chromatin interaction
ENSG00000129514	Chromatin interaction
ENSG00000108423	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10142669	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10142891	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10145423	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10148570	1.00[CEU][hapmap];0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10148682	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10148961	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10149383	1.00[CEU][hapmap];0.87[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10150735	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10150916	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11846887	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11848128	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11848510	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11849527	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11849571	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11850109	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17092556	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17102606	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17102889	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17103007	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17103550	1.00[CEU][hapmap]
rs1957415	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28510166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28609318	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8014450	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8016283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8016287	1.00[AMR][1000 genomes]
rs9322956	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv530770	chr14:21526410-21852363	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers 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	57 gene(s)	inside rSNPs	diseases
7	nsv1043570	chr14:21575068-21899964	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv541977	chr14:21575068-21899964	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1048032	chr14:21602341-21847247	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
10	nsv541978	chr14:21602341-21847247	Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS 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	29 gene(s)	inside rSNPs	diseases
11	nsv948957	chr14:21616875-21928338	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription 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
12	nsv901477	chr14:21625262-21750308	Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
13	nsv901478	chr14:21626497-21750308	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
14	nsv1044822	chr14:21659344-21860081	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	nsv541980	chr14:21672540-21742729	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
16	nsv541983	chr14:21676221-21742729	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
17	esv1825348	chr14:21691941-21829404	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS 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 miRNA target site	18 gene(s)	inside rSNPs	diseases
18	nsv1051407	chr14:21692670-21907366	Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv541984	chr14:21692670-21907366	Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
20	nsv530010	chr14:21692670-21923767	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
21	nsv541987	chr14:21692703-21742729	Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
22	nsv541989	chr14:21696056-21742729	Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
23	esv3357025	chr14:21702262-21737534	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
24	nsv541990	chr14:21702771-21757737	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
25	nsv428617	chr14:21721165-21871164	Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers 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 miRNA target site	32 gene(s)	inside rSNPs	diseases
26	nsv983804	chr14:21730434-21759672	Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21728600-21737400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
2	chr14:21729200-21736800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
3	chr14:21730200-21737600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
4	chr14:21730800-21736800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr14:21731600-21736800	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
6	chr14:21731600-21737000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
7	chr14:21731600-21737200	Transcr. at gene 5' and 3'	A549	lung
8	chr14:21731600-21737400	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
9	chr14:21731800-21736800	Transcr. at gene 5' and 3'	HUVEC	blood vessel
10	chr14:21731800-21737200	Transcr. at gene 5' and 3'	Dnd41	blood
11	chr14:21731800-21737400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
12	chr14:21732000-21736800	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
13	chr14:21732800-21737200	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
14	chr14:21733000-21737600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr14:21733600-21736800	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine
16	chr14:21733800-21736800	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:21733800-21736800	Transcr. at gene 5' and 3'	Osteobl	bone
18	chr14:21734000-21737600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr14:21734000-21737800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr14:21734000-21738400	Active TSS	Right Ventricle	heart
21	chr14:21734000-21738600	Active TSS	Psoas Muscle	Psoas
22	chr14:21734200-21736800	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr14:21734200-21737600	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr14:21734200-21737800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr14:21734200-21738000	Active TSS	Rectal Smooth Muscle	rectum
26	chr14:21734200-21738400	Active TSS	H9 Cell Line	embryonic stem cell
27	chr14:21734400-21736600	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr14:21734400-21736800	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
29	chr14:21734600-21736600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr14:21734600-21736600	Weak transcription	Esophagus	oesophagus
31	chr14:21734600-21736600	Weak transcription	Gastric	stomach
32	chr14:21734600-21737000	Weak transcription	Spleen	Spleen
33	chr14:21734600-21737800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:21734600-21738200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr14:21734800-21736800	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
36	chr14:21734800-21736800	Transcr. at gene 5' and 3'	HSMM	muscle
37	chr14:21734800-21737600	Active TSS	Ovary	ovary
38	chr14:21734800-21737600	Active TSS	NHLF	lung
39	chr14:21734800-21738200	Active TSS	Right Atrium	heart
40	chr14:21734800-21738600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr14:21735000-21736800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
42	chr14:21735000-21736800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr14:21735000-21737000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:21735000-21737600	Active TSS	Placenta	Placenta
45	chr14:21735000-21737600	Active TSS	Pancreas	Pancrea
46	chr14:21735000-21738000	Active TSS	Duodenum Mucosa	Duodenum
47	chr14:21735000-21738000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
48	chr14:21735000-21738000	Active TSS	Stomach Smooth Muscle	stomach
49	chr14:21735000-21738200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:21735000-21738200	Active TSS	Duodenum Smooth Muscle	Duodenum

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