Variant report

Variant	rs7665125
Chromosome Location	chr4:120402079-120402080
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:120401525..120403278-chr4:120407490..120410209,2	MCF-7	breast:
2	chr4:120372429..120374699-chr4:120400382..120402462,2	K562	blood:
3	chr4:120395792..120397416-chr4:120401451..120404061,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-8	chr4:120401906-120402691	NONHSAT098084

Variant related genes	Relation type
ENSG00000245958	Chromatin interaction

Extended variants
information (count: 193 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:180)

rs_ID	r²[population]
rs10003567	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs10006259	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs10006525	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10006706	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10006793	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10006877	0.90[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap]
rs10008459	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10009450	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10009626	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs10013042	0.85[JPT][hapmap]
rs10013305	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs10017335	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs10018280	0.82[CEU][hapmap];0.80[CHB][hapmap];0.95[JPT][hapmap]
rs10018726	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10019674	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs10026516	0.80[ASN][1000 genomes]
rs10026736	0.82[ASN][1000 genomes]
rs10026952	0.81[ASN][1000 genomes]
rs10030660	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs10031483	0.90[CEU][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10031665	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10032151	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10032158	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10034623	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1010739	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs1010740	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs10518300	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs10518328	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10518329	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11098501	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs11098506	1.00[CEU][hapmap];0.96[CHB][hapmap];0.83[JPT][hapmap]
rs11098524	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11098525	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11098526	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11098527	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11098530	0.90[CEU][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11098531	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs1155576	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs11723090	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs11729521	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11731756	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs11734241	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11737395	0.95[JPT][hapmap]
rs11933966	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs11934314	0.81[ASN][1000 genomes]
rs11934940	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11935596	0.90[CEU][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11940028	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11943877	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11947234	0.90[CEU][hapmap];0.95[JPT][hapmap]
rs12498599	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs12499324	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12502423	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12505735	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs12505953	0.83[ASN][1000 genomes]
rs12507565	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs12507964	0.90[CEU][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12508504	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12510138	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12511640	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs12513083	0.82[CHB][hapmap];0.80[JPT][hapmap]
rs12711071	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs13104219	0.82[CHB][hapmap]
rs13107475	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13128602	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs13134517	0.87[CHB][hapmap]
rs13134665	0.89[CEU][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs13145352	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13149407	0.91[JPT][hapmap]
rs1383532	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs1480930	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1480931	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1480933	0.82[CHB][hapmap]
rs1480936	0.84[CEU][hapmap];0.90[JPT][hapmap]
rs1480940	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs1511017	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs1511025	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs1546502	0.90[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap]
rs1546503	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs1546505	0.89[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap]
rs1552092	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs1552095	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs17005535	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17006190	0.90[CEU][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17046116	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17046118	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17050695	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs1980025	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1980026	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs2127821	0.88[CEU][hapmap];0.95[JPT][hapmap]
rs2127823	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs2170276	0.83[CEU][hapmap];0.95[JPT][hapmap]
rs2291185	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs2306455	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2306456	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs2389803	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2389809	0.90[CEU][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs28374462	0.82[ASN][1000 genomes]
rs28441656	0.80[ASN][1000 genomes]
rs28444327	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28461559	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28479042	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28499576	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28535956	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs28559989	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28571712	0.81[ASN][1000 genomes]
rs28578366	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs28587142	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28632018	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28685688	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28845498	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2892848	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs34858317	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35063680	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3733519	0.86[CEU][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3733520	0.90[CEU][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3733523	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3733524	0.89[CEU][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3736115	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs3756156	0.95[JPT][hapmap]
rs3775841	0.83[CEU][hapmap];0.95[JPT][hapmap]
rs3775843	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs3775844	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs3775845	0.83[CEU][hapmap];0.95[JPT][hapmap]
rs3775848	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs3775852	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs3806808	0.86[JPT][hapmap]
rs3822192	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs3822194	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs3822195	0.83[CEU][hapmap];0.95[JPT][hapmap]
rs41464847	0.87[CHB][hapmap]
rs4577559	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56270433	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6534139	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs6820115	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6822679	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6824111	1.00[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap]
rs6832740	0.95[JPT][hapmap]
rs6834796	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6835635	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs6837828	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6838814	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6842762	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6843229	0.86[CHB][hapmap]
rs6844263	0.83[CHB][hapmap]
rs6848389	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6849171	0.90[CEU][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6849561	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6853998	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs714899	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs71614444	0.81[ASN][1000 genomes]
rs71614448	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71614449	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7436506	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7654529	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7654546	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7654587	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7656252	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7659336	0.80[ASN][1000 genomes]
rs7659501	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs7672594	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs7681214	0.80[ASN][1000 genomes]
rs7681544	0.90[CEU][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7681978	0.83[ASN][1000 genomes]
rs7687843	0.90[CEU][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7688802	0.89[CEU][hapmap];0.95[JPT][hapmap]
rs7692994	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7695620	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs7699064	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap]
rs878372	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs907205	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs9884402	0.84[CEU][hapmap];0.95[JPT][hapmap]
rs9991959	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs9993199	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9994730	0.81[ASN][1000 genomes]
rs9994810	0.81[ASN][1000 genomes]
rs9995136	1.00[CEU][hapmap];0.96[CHB][hapmap];0.83[JPT][hapmap]
rs9997631	0.82[CEU][hapmap];0.95[JPT][hapmap]
rs9998585	0.90[CEU][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9999724	0.80[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv879842	chr4:120244085-120424087	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv427694	chr4:120250511-120501728	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv879843	chr4:120326323-120502461	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv879844	chr4:120341296-120449810	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv879846	chr4:120341296-120491714	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv879845	chr4:120341296-120502461	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv879847	chr4:120371729-120450159	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv964092	chr4:120392750-120412350	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	esv1802153	chr4:120397829-120457682	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs7665125	LOC284701///FLJ14186///LOC441124///LOC641693///LOC642788///LOC653056	cis	normal skin	skin_eQTL
rs7665125	RP11-33B1.4	cis	Whole Blood	GTEx
rs7665125	RP11-33B1.1	cis	Heart Left Ventricle	GTEx
rs7665125	FLJ14186///LOC284701///LOC441124///LOC728624	Cis_1M	lymphoblastoid	RTeQTL
rs7665125	RP11-33B1.1	cis	Whole Blood	GTEx
rs7665125	RP11-33B1.1	cis	lung	GTEx
rs7665125	RP11-33B1.1	cis	Nerve Tibial	GTEx
rs7665125	RP11-33B1.1	cis	Artery Tibial	GTEx
rs7665125	RP11-384K6.6	cis	Whole Blood	GTEx
rs7665125	RP11-33B1.1	cis	Esophagus Mucosa	GTEx
rs7665125	LOC645513	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120376400-120471600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:120376600-120419200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr4:120377000-120416000	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:120377200-120403400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:120377200-120415600	Weak transcription	Brain Substantia Nigra	brain
6	chr4:120377200-120416200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr4:120377200-120419600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:120377200-120433800	Weak transcription	Gastric	stomach
9	chr4:120377400-120403000	Weak transcription	Fetal Brain Female	brain
10	chr4:120377400-120415200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr4:120377400-120416200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr4:120377400-120439000	Weak transcription	Small Intestine	intestine
13	chr4:120377400-120439000	Weak transcription	Spleen	Spleen
14	chr4:120377600-120402200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:120377600-120403000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr4:120377600-120441000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr4:120377600-120501200	Weak transcription	Pancreas	Pancrea
18	chr4:120384400-120439200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr4:120384600-120416200	Weak transcription	Fetal Brain Male	brain
20	chr4:120385600-120403000	Weak transcription	Fetal Kidney	kidney
21	chr4:120387000-120402600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:120387400-120403600	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr4:120388600-120402400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:120390400-120409400	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr4:120390600-120409200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:120390800-120419800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr4:120391600-120408800	Weak transcription	NHDF-Ad	bronchial
28	chr4:120391600-120415600	Weak transcription	HUVEC	blood vessel
29	chr4:120392400-120402600	Strong transcription	HSMM	muscle
30	chr4:120392600-120402400	Strong transcription	Fetal Thymus	thymus
31	chr4:120393200-120419800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr4:120393800-120409800	Weak transcription	NH-A	brain
33	chr4:120394800-120415200	Weak transcription	NHEK	skin
34	chr4:120395600-120404800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:120396000-120404000	Strong transcription	Dnd41	blood
36	chr4:120396200-120402800	Strong transcription	Primary T cells from cord blood	blood
37	chr4:120396800-120402200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr4:120397000-120403400	Strong transcription	Placenta	Placenta
39	chr4:120397200-120402200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr4:120397200-120403600	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr4:120397600-120415000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr4:120397800-120403200	Weak transcription	Fetal Lung	lung
43	chr4:120397800-120404800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr4:120397800-120416400	Weak transcription	HSMMtube	muscle
45	chr4:120397800-120442600	Weak transcription	Hela-S3	cervix
46	chr4:120398200-120419600	Weak transcription	Fetal Stomach	stomach
47	chr4:120398400-120402200	Enhancers	Fetal Intestine Small	intestine
48	chr4:120398400-120403800	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr4:120398600-120402400	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr4:120398600-120402400	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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