Variant report

Variant	rs7668661
Chromosome Location	chr4:1300172-1300173
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUND	chr4:1299889-1300208	HepG2	liver:	n/a	chr4:1300048-1300059
2	JUN	chr4:1299696-1300314	K562	blood:	n/a	n/a
3	STAT3	chr4:1299875-1300202	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr4:1299905-1300206	MCF10A-Er-Src	breast:	n/a	n/a
5	ATF3	chr4:1299875-1300211	K562	blood:	n/a	n/a
6	POU2F2	chr4:1299833-1300221	GM12891	blood:	n/a	chr4:1300031-1300044
7	POU2F2	chr4:1299910-1300215	GM12878	blood:	n/a	chr4:1300031-1300044
8	FOSL1	chr4:1298902-1300342	HCT-116	colon:	n/a	n/a
9	POLR2A	chr4:1299393-1301435	K562	blood:	n/a	n/a
10	POU2F2	chr4:1299761-1300270	GM12878	blood:	n/a	chr4:1300031-1300044
11	JUND	chr4:1299875-1300212	K562	blood:	n/a	chr4:1300048-1300059
12	POU2F2	chr4:1299823-1300224	GM12891	blood:	n/a	chr4:1300031-1300044
13	FOS	chr4:1299897-1300227	MCF10A-Er-Src	breast:	n/a	n/a
14	STAT3	chr4:1299905-1300236	MCF10A-Er-Src	breast:	n/a	n/a
15	RUNX3	chr4:1299834-1300202	GM12878	blood:	n/a	n/a
16	STAT3	chr4:1299893-1300234	MCF10A-Er-Src	breast:	n/a	n/a
17	JUND	chr4:1298851-1300376	HCT-116	colon:	n/a	chr4:1300048-1300059 chr4:1299313-1299324
18	FOS	chr4:1299911-1300195	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr4:1299892-1300212	MCF10A-Er-Src	breast:	n/a	n/a
20	FOSL1	chr4:1299859-1300233	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1300163-1300213	MCF-7	breast:	n/a
2	chr4:1300163-1300213	GM12878	blood:	n/a
3	chr4:1300163-1300213	HIPEpiC	eye:	n/a
4	chr4:1300163-1300213	HNPCEpiC	eye:	n/a
5	chr4:1300163-1300213	SK-N-SH	brain:	n/a
6	chr4:1300163-1300213	HEEpiC	esophagus:	n/a
7	chr4:1300163-1300213	SAEC	small airway:	n/a
8	chr4:1300163-1300213	GM06990	blood:	n/a
9	chr4:1300163-1300213	HAEpiC	amniotic membrane:	n/a
10	chr4:1300163-1300213	HCM	heart:	n/a
11	chr4:1300163-1300213	A549	lung:	n/a
12	chr4:1300163-1300213	HRCEpiC	kidney:	n/a
13	chr4:1300163-1300213	H1-hESC	embryonic stem cell:	embryo
14	chr4:1300163-1300213	HCF	heart:	n/a
15	chr4:1300163-1300213	NT2-D1	testis:	n/a
16	chr4:1300163-1300213	ECC-1	luminal epithelium:	n/a
17	chr4:1300163-1300213	GM12891	blood:	n/a
18	chr4:1300163-1300213	PrEC	prostate:	n/a
19	chr4:1300163-1300213	T-47D	breast:	n/a
20	chr4:1300163-1300213	HRPEpiC	eye:	n/a
21	chr4:1300163-1300213	Jurkat	blood:	n/a
22	chr4:1300163-1300213	SK-N-SH_RA	brain:	n/a
23	chr4:1300163-1300213	Hepatocyte	liver:	n/a
24	chr4:1300163-1300213	NHDF-neo	bronchial:	n/a
25	chr4:1300163-1300213	AG04450	lung:	fetal
26	chr4:1300163-1300213	K562	blood:	n/a
27	chr4:1300163-1300213	PFSK-1	brain:	n/a
28	chr4:1300163-1300213	HepG2	liver:	n/a
29	chr4:1300163-1300213	HRE	kidney:	n/a
30	chr4:1300163-1300213	U87	brain:	n/a
31	chr4:1300163-1300213	BJ	skin:	n/a
32	chr4:1300163-1300213	AG10803	skin:	n/a
33	chr4:1300163-1300213	SKMC	muscle:	n/a
34	chr4:1300163-1300213	BE2_C	brain:	n/a
35	chr4:1300163-1300213	NB4	blood:	n/a
36	chr4:1300163-1300213	NH-A	brain:	n/a
37	chr4:1300163-1300213	RPTEC	kidney:	n/a
38	chr4:1300163-1300213	GM12892	blood:	n/a
39	chr4:1300163-1300213	HL-60	blood:	n/a
40	chr4:1300163-1300213	HCT-116	colon:	n/a
41	chr4:1300163-1300213	HUVEC	blood vessel:	n/a
42	chr4:1300163-1300213	AG04449	skin:	fetal
43	chr4:1300163-1300213	GM19239	blood:	n/a
44	chr4:1300163-1300213	SK-N-MC	brain:	n/a
45	chr4:1300163-1300213	LNCaP	prostate:	n/a
46	chr4:1300163-1300213	CMK	blood:	n/a
47	chr4:1300163-1300213	HMEC	breast:	n/a
48	chr4:1300163-1300213	IMR90	lung:	fetal
49	chr4:1300163-1300213	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:1300163-1300213	PANC-1	pancreas:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1298051..1300752-chr4:1304629..1306876,2	MCF-7	breast:
2	chr4:1232098..1233809-chr4:1299016..1301525,2	K562	blood:
3	chr4:1299735..1301885-chr4:1304010..1308406,3	MCF-7	breast:
4	chr4:1240987..1244613-chr4:1297662..1300562,3	MCF-7	breast:

No data

Variant related genes	Relation type
MAEA	TF binding region
MAEA	CpG island
ENSG00000196810	Chromatin interaction
ENSG00000159692	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10000874	0.85[EUR][1000 genomes]
rs10023922	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10024013	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11247984	0.83[EUR][1000 genomes]
rs11247986	0.82[EUR][1000 genomes]
rs11247987	0.83[EUR][1000 genomes]
rs12509700	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12641735	0.95[EUR][1000 genomes]
rs12642396	0.83[EUR][1000 genomes]
rs12642410	0.88[EUR][1000 genomes]
rs13109112	0.83[EUR][1000 genomes]
rs13112706	0.89[EUR][1000 genomes]
rs13119532	0.89[EUR][1000 genomes]
rs13124383	0.89[EUR][1000 genomes]
rs13128045	0.89[EUR][1000 genomes]
rs13134106	0.89[EUR][1000 genomes]
rs13142772	0.89[EUR][1000 genomes]
rs13149952	0.89[EUR][1000 genomes]
rs1316419	0.83[EUR][1000 genomes]
rs1620928	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1680072	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1680073	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1680074	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1732099	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1732100	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1732102	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2293633	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2293634	0.90[EUR][1000 genomes]
rs2293635	0.83[EUR][1000 genomes]
rs35201724	0.81[EUR][1000 genomes]
rs4974584	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4974594	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4974596	0.89[EUR][1000 genomes]
rs62293658	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs66987549	0.81[EUR][1000 genomes]
rs6826029	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6851528	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7673398	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7695691	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs922698	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9631804	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9631805	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9992932	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9992934	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 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	nsv829835	chr4:1097586-1304239	Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription 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	59 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	nsv461156	chr4:1254930-1312394	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Enhancers 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	16 gene(s)	inside rSNPs	diseases
16	nsv593299	chr4:1254930-1312394	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS 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	16 gene(s)	inside rSNPs	diseases
17	nsv593300	chr4:1272664-1312394	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs7668661	CTBP1	Cis_1M	lymphoblastoid	RTeQTL
rs7668661	UVSSA	cis	Skin Sun Exposed Lower leg	GTEx
rs7668661	CRIPAK	cis	Artery Aorta	GTEx
rs7668661	UVSSA	cis	Thyroid	GTEx
rs7668661	UVSSA	cis	Stomach	GTEx
rs7668661	UVSSA	cis	Whole Blood	GTEx
rs7668661	CRIPAK	cis	Thyroid	GTEx
rs7668661	MAEA	cis	Nerve Tibial	GTEx
rs7668661	MAEA	cis	Thyroid	GTEx
rs7668661	UVSSA	cis	Artery Aorta	GTEx
rs7668661	CTBP1	cis	multi-tissue	Pritchard

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1285200-1303400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:1285400-1302400	Weak transcription	Fetal Kidney	kidney
3	chr4:1285800-1302200	Weak transcription	NHDF-Ad	bronchial
4	chr4:1286200-1302400	Weak transcription	Fetal Brain Male	brain
5	chr4:1289400-1302200	Weak transcription	Fetal Heart	heart
6	chr4:1290000-1302400	Strong transcription	Fetal Stomach	stomach
7	chr4:1290400-1301200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:1290400-1302200	Weak transcription	Right Atrium	heart
9	chr4:1290800-1302600	Weak transcription	Colon Smooth Muscle	Colon
10	chr4:1292000-1302200	Weak transcription	Fetal Lung	lung
11	chr4:1292000-1302600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:1292000-1302600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr4:1292000-1303400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr4:1292600-1302200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr4:1293200-1312000	Weak transcription	Hela-S3	cervix
16	chr4:1293600-1301800	Weak transcription	Brain Anterior Caudate	brain
17	chr4:1293800-1302200	Weak transcription	Brain Cingulate Gyrus	brain
18	chr4:1293800-1303400	Weak transcription	Aorta	Aorta
19	chr4:1294200-1302000	Weak transcription	Osteobl	bone
20	chr4:1294400-1301800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr4:1294400-1302200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:1294400-1302600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr4:1294600-1300600	Weak transcription	Psoas Muscle	Psoas
24	chr4:1294600-1301000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:1294800-1302000	Weak transcription	Brain Angular Gyrus	brain
26	chr4:1294800-1302200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr4:1294800-1302200	Weak transcription	Brain Substantia Nigra	brain
28	chr4:1295000-1301400	Weak transcription	NHLF	lung
29	chr4:1295000-1302000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr4:1295000-1302400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:1295000-1302600	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr4:1295200-1301800	Weak transcription	Left Ventricle	heart
33	chr4:1295200-1302000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr4:1295200-1302600	Weak transcription	Brain Germinal Matrix	brain
35	chr4:1295200-1303400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr4:1295200-1303400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:1295400-1300400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr4:1295400-1302800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr4:1295400-1302800	Weak transcription	NH-A	brain
40	chr4:1295600-1302000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr4:1295600-1302000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr4:1295600-1302200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr4:1295800-1301800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:1295800-1302600	Weak transcription	HSMMtube	muscle
45	chr4:1296000-1301800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:1296000-1302000	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr4:1296000-1302600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:1296000-1302600	Weak transcription	HUVEC	blood vessel
49	chr4:1296200-1302400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:1296200-1302800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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