Variant report

Variant	rs1316393
Chromosome Location	chr4:1315619-1315620
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:1281929..1283740-chr4:1313199..1316127,2	MCF-7	breast:
2	chr4:1307443..1309271-chr4:1314999..1317229,2	K562	blood:
3	chr4:1314077..1316689-chr4:1338914..1341716,2	MCF-7	breast:
4	chr4:1282487..1285160-chr4:1313904..1316772,2	MCF-7	breast:
5	chr4:1310884..1316010-chr4:1322677..1327905,6	MCF-7	breast:
6	chr4:1240559..1242857-chr4:1315029..1317757,2	MCF-7	breast:
7	chr4:1241359..1243168-chr4:1314910..1317673,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000090316	Chromatin interaction
ENSG00000196810	Chromatin interaction
ENSG00000163945	Chromatin interaction
ENSG00000159692	Chromatin interaction

Extended variants
information (count: 101 )
Associated
traits (count: 17 )

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs11247983	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11247994	0.82[ASW][hapmap];0.83[JPT][hapmap]
rs11247996	0.83[JPT][hapmap]
rs11721789	0.81[CEU][hapmap];1.00[YRI][hapmap]
rs11727167	0.84[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.81[TSI][hapmap];1.00[YRI][hapmap]
rs12499546	0.82[CEU][hapmap]
rs12502916	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12508446	0.88[CEU][hapmap]
rs12512607	0.82[ASW][hapmap];1.00[YRI][hapmap]
rs12641735	0.81[CEU][hapmap]
rs12642410	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[ASN][1000 genomes]
rs12647145	1.00[CHB][hapmap]
rs13103860	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13110563	0.82[CEU][hapmap];1.00[YRI][hapmap]
rs13112706	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13114968	0.90[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs13115173	0.92[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13124383	0.82[AFR][1000 genomes]
rs13128045	0.96[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13128825	0.83[ASN][1000 genomes]
rs13134106	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13134568	0.83[ASN][1000 genomes]
rs13135102	0.82[ASW][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs13141992	0.82[ASW][hapmap];0.83[JPT][hapmap]
rs13142772	0.82[AFR][1000 genomes]
rs13145722	0.83[ASN][1000 genomes]
rs13149575	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.81[TSI][hapmap]
rs13149952	1.00[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];0.82[ASN][1000 genomes]
rs13150571	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1316394	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1564508	0.82[CEU][hapmap]
rs1680073	0.81[CEU][hapmap]
rs1680074	0.81[CEU][hapmap]
rs1732100	0.81[CEU][hapmap]
rs1732107	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1960426	0.82[CEU][hapmap];0.89[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap]
rs2199956	0.81[CEU][hapmap]
rs2279281	0.81[CEU][hapmap]
rs2291199	0.84[ASW][hapmap];0.82[CEU][hapmap];1.00[YRI][hapmap]
rs2335855	0.82[CEU][hapmap]
rs35201724	0.85[ASN][1000 genomes]
rs35705197	0.83[ASN][1000 genomes]
rs3755920	0.81[CEU][hapmap]
rs3775099	1.00[YRI][hapmap]
rs3796616	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs3915420	0.82[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4045131	1.00[YRI][hapmap]
rs4246685	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4405964	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4428235	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4493483	0.96[CEU][hapmap];0.89[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs4516656	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4519749	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4642180	0.96[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4974551	0.83[ASN][1000 genomes]
rs4974552	0.83[ASN][1000 genomes]
rs4974574	1.00[YRI][hapmap]
rs4974582	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4974594	0.81[CEU][hapmap]
rs4974602	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs4974603	0.83[JPT][hapmap]
rs56115381	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6822570	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs6826415	1.00[ASW][hapmap];0.83[JPT][hapmap]
rs7671242	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7673398	0.81[CEU][hapmap]
rs7695691	0.81[CEU][hapmap]
rs900027	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs900028	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs900029	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs922698	0.81[CEU][hapmap]
rs9631804	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv878328	chr4:1141573-1990425	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
5	nsv878330	chr4:1147407-1523930	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
6	nsv461152	chr4:1159680-1415698	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
7	nsv593278	chr4:1159680-1415698	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
8	nsv997971	chr4:1191256-1518521	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer 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 miRNA target site	67 gene(s)	inside rSNPs	diseases
9	nsv461155	chr4:1203265-1352685	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Weak transcription Active 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	66 gene(s)	inside rSNPs	diseases
10	nsv593281	chr4:1203265-1352685	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
11	nsv1002097	chr4:1212573-1320086	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers 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	51 gene(s)	inside rSNPs	diseases
12	nsv536986	chr4:1212573-1320086	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
13	nsv593298	chr4:1244267-1342521	Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
14	nsv878338	chr4:1277826-1358449	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
15	nsv878339	chr4:1277826-1363886	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
16	nsv878340	chr4:1277826-1386570	Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
17	nsv878341	chr4:1277826-1391400	Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
18	nsv1002635	chr4:1282603-1402761	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
19	nsv878342	chr4:1291337-1363886	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
20	nsv878343	chr4:1291337-1391400	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS 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	30 gene(s)	inside rSNPs	diseases
21	nsv878344	chr4:1291337-1414684	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
22	nsv878345	chr4:1291337-1563920	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
23	nsv461157	chr4:1300077-1352685	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
24	nsv593301	chr4:1300077-1352685	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
25	nsv878346	chr4:1300077-1363886	Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
26	nsv878347	chr4:1300077-1866358	Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
27	nsv878348	chr4:1305269-1386570	Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
28	esv1833544	chr4:1305962-1327941	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
29	esv1794294	chr4:1307119-1817474	Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases

mRNA abundance (count:17)

SNP	Gene	Cis/trans	Tissue	Source
rs1316393	UVSSA	cis	Whole Blood	GTEx
rs1316393	CRIPAK	cis	parietal	SCAN
rs1316393	UVSSA	cis	Thyroid	GTEx
rs1316393	MAEA	cis	Thyroid	GTEx
rs1316393	KIAA1530	cis	multi-tissue	Pritchard
rs1316393	KIAA1530	cis	parietal	SCAN
rs1316393	ADD1	cis	cerebellum	SCAN
rs1316393	SPON2	cis	multi-tissue	Pritchard
rs1316393	KIAA1530	cis	cerebellum	SCAN
rs1316393	MAEA	cis	Nerve Tibial	GTEx
rs1316393	UVSSA	cis	Stomach	GTEx
rs1316393	MAEA	cis	cerebellum	SCAN
rs1316393	CRIPAK	cis	cerebellum	SCAN
rs1316393	CRIPAK	cis	Thyroid	GTEx
rs1316393	C4orf42	cis	cerebellum	SCAN
rs1316393	CTBP1	cis	multi-tissue	Pritchard
rs1316393	UVSSA	cis	Skin Sun Exposed Lower leg	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1303600-1339400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:1304400-1317200	Weak transcription	HSMMtube	muscle
3	chr4:1304400-1317400	Weak transcription	Fetal Brain Male	brain
4	chr4:1305000-1327200	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr4:1305200-1326600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr4:1305200-1330200	Weak transcription	Fetal Heart	heart
7	chr4:1305400-1316000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:1305800-1317400	Weak transcription	Right Atrium	heart
9	chr4:1306000-1323400	Strong transcription	Fetal Muscle Trunk	muscle
10	chr4:1306200-1322200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:1308800-1321200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:1309200-1330400	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr4:1309400-1317000	Weak transcription	NH-A	brain
14	chr4:1310400-1316400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr4:1310600-1317400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr4:1310600-1321400	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr4:1310800-1321800	Strong transcription	Primary T cells from cord blood	blood
18	chr4:1310800-1323200	Weak transcription	Psoas Muscle	Psoas
19	chr4:1311200-1321000	Weak transcription	Small Intestine	intestine
20	chr4:1311800-1321000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr4:1311800-1322400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr4:1312200-1317000	Weak transcription	Stomach Mucosa	stomach
23	chr4:1312200-1321800	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr4:1312600-1316200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr4:1312800-1317000	Weak transcription	HUVEC	blood vessel
26	chr4:1312800-1317200	Weak transcription	NHDF-Ad	bronchial
27	chr4:1312800-1317400	Weak transcription	Brain Substantia Nigra	brain
28	chr4:1313000-1317400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:1313000-1318800	Weak transcription	Aorta	Aorta
30	chr4:1313200-1316000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr4:1313200-1316000	Weak transcription	Colon Smooth Muscle	Colon
32	chr4:1313200-1316400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr4:1313200-1317000	Weak transcription	Hela-S3	cervix
34	chr4:1313200-1317600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr4:1313400-1315800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:1313400-1315800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr4:1313400-1316000	Weak transcription	Gastric	stomach
38	chr4:1313400-1316200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:1313400-1316200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr4:1313400-1316200	Weak transcription	K562	blood
41	chr4:1313400-1317200	Weak transcription	Primary B cells from cord blood	blood
42	chr4:1313400-1320800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:1313600-1315800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr4:1313600-1315800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr4:1313600-1315800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:1313600-1315800	Weak transcription	Brain Angular Gyrus	brain
47	chr4:1313600-1315800	Weak transcription	Fetal Intestine Large	intestine
48	chr4:1313600-1315800	Weak transcription	A549	lung
49	chr4:1313600-1316000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr4:1313600-1316000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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