Variant report

Variant	rs649101
Chromosome Location	chr1:10490111-10490112
allele	C/T
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	EGR1	chr1:10490088-10491191	HCT-116	colon:	n/a	chr1:10490750-10490759 chr1:10490721-10490735 chr1:10490350-10490360
2	POLR2A	chr1:10490008-10491366	GM12878	blood:	n/a	n/a
3	POLR2A	chr1:10490088-10491011	K562	blood:	n/a	n/a
4	JUND	chr1:10490031-10491147	K562	blood:	n/a	n/a
5	FOXM1	chr1:10490105-10491180	GM12878	blood:	n/a	n/a
6	MAX	chr1:10489978-10491108	HUVEC	blood vessel:	n/a	chr1:10490255-10490262
7	TBL1XR1	chr1:10490105-10491547	K562	blood:	n/a	n/a
8	POLR2A	chr1:10490001-10491062	GM12891	blood:	n/a	n/a
9	SIN3AK20	chr1:10490052-10491405	PANC-1	pancreas:	n/a	n/a
10	EP300	chr1:10490096-10490461	K562	blood:	n/a	n/a
11	POLR2A	chr1:10490088-10491133	PANC-1	pancreas:	n/a	n/a
12	KAP1	chr1:10490063-10490709	HEK293	kidney:	n/a	n/a
13	ATF2	chr1:10490050-10491090	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr1:10490083-10491658	HepG2	liver:	n/a	n/a
15	MAZ	chr1:10489707-10491577	IMR90	lung:	n/a	chr1:10490255-10490262
16	SMC3	chr1:10489751-10491449	SK-N-SH	brain:	n/a	chr1:10490428-10490438 chr1:10490424-10490438
17	HA-E2F1	chr1:10489950-10491592	MCF-7	breast:	n/a	chr1:10490750-10490759 chr1:10490696-10490706 chr1:10490431-10490440
18	MXI1	chr1:10490029-10491225	GM12878	blood:	n/a	chr1:10490791-10490806
19	MAX	chr1:10490078-10491505	HepG2	liver:	n/a	chr1:10490255-10490262
20	E2F6	chr1:10490010-10491552	H1-hESC	embryonic stem cell:	n/a	chr1:10490750-10490759 chr1:10490696-10490706 chr1:10490431-10490440 chr1:10490495-10490506
21	MAX	chr1:10490019-10491554	H1-hESC	embryonic stem cell:	n/a	chr1:10490255-10490262
22	CREB1	chr1:10489834-10491148	GM12878	blood:	n/a	n/a
23	PML	chr1:10489957-10491391	GM12878	blood:	n/a	n/a
24	MXI1	chr1:10489861-10491608	IMR90	lung:	n/a	chr1:10490791-10490806
25	MAX	chr1:10490006-10491361	MCF-7	breast:	n/a	chr1:10490255-10490262
26	POLR2A	chr1:10489904-10491135	HUVEC	blood vessel:	n/a	n/a
27	MYC	chr1:10490095-10491330	K562	blood:	n/a	chr1:10490255-10490262
28	GATA2	chr1:10489832-10490480	HUVEC	blood vessel:	n/a	n/a
29	REST	chr1:10489888-10491538	H1-neurons	neurons:	n/a	chr1:10490770-10490783 chr1:10490697-10490707
30	POLR2A	chr1:10490092-10491064	K562	blood:	n/a	n/a
31	MTA3	chr1:10489921-10491265	GM12878	blood:	n/a	n/a
32	MXI1	chr1:10489950-10491658	SK-N-SH	brain:	n/a	chr1:10490791-10490806
33	CTCF	chr1:10490060-10490210	HCM	heart:	n/a	n/a
34	POLR2A	chr1:10490063-10491434	H1-neurons	neurons:	n/a	n/a
35	RAD21	chr1:10489837-10491455	SK-N-SH	brain:	n/a	chr1:10490428-10490438 chr1:10490378-10490388 chr1:10490696-10490709 chr1:10490423-10490442
36	CTCF	chr1:10490098-10491052	K562	blood:	n/a	chr1:10490427-10490437 chr1:10490422-10490440 chr1:10490425-10490438 chr1:10490423-10490439 chr1:10490696-10490709 chr1:10490425-10490438 chr1:10490425-10490434
37	SMC3	chr1:10489966-10491022	GM12878	blood:	n/a	chr1:10490428-10490438 chr1:10490424-10490438
38	CREB1	chr1:10490051-10491363	H1-hESC	embryonic stem cell:	n/a	n/a
39	SP1	chr1:10490044-10490866	A549	lung:	n/a	n/a
40	TEAD4	chr1:10490072-10491170	K562	blood:	n/a	n/a
41	MAX	chr1:10490021-10491522	H1-hESC	embryonic stem cell:	n/a	chr1:10490255-10490262
42	RELA	chr1:10490055-10491417	GM10847	blood:	n/a	n/a
43	RUNX3	chr1:10490087-10491345	GM12878	blood:	n/a	chr1:10490788-10490805
44	POLR2A	chr1:10490043-10491305	GM12891	blood:	n/a	n/a
45	RUNX3	chr1:10489882-10490698	GM12878	blood:	n/a	n/a
46	SPI1	chr1:10489944-10490129	K562	blood:	n/a	chr1:10490028-10490037
47	MBD4	chr1:10489996-10490545	HepG2	liver:	n/a	n/a
48	JUN	chr1:10489840-10491572	K562	blood:	n/a	n/a
49	BCLAF1	chr1:10490079-10490957	GM12878	blood:	n/a	chr1:10490694-10490707
50	E2F6	chr1:10489951-10491580	K562	blood:	n/a	chr1:10490750-10490759 chr1:10490696-10490706 chr1:10490431-10490440 chr1:10490495-10490506

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10490063-10490113	PFSK-1	brain:	n/a
2	chr1:10490063-10490113	H1-hESC	embryonic stem cell:	embryo
3	chr1:10490063-10490113	Hepatocyte	liver:	n/a
4	chr1:10490063-10490113	SK-N-MC	brain:	n/a
5	chr1:10490063-10490113	BE2_C	brain:	n/a
6	chr1:10490063-10490113	NB4	blood:	n/a
7	chr1:10490063-10490113	A549	lung:	n/a
8	chr1:10490063-10490113	HEEpiC	esophagus:	n/a
9	chr1:10490063-10490113	PANC-1	pancreas:	n/a
10	chr1:10490063-10490113	SAEC	small airway:	n/a
11	chr1:10490063-10490113	GM19239	blood:	n/a
12	chr1:10490063-10490113	Jurkat	blood:	n/a
13	chr1:10490063-10490113	U87	brain:	n/a
14	chr1:10490063-10490113	CMK	blood:	n/a
15	chr1:10490063-10490113	HCM	heart:	n/a
16	chr1:10490063-10490113	ECC-1	luminal epithelium:	n/a
17	chr1:10490063-10490113	HMEC	breast:	n/a
18	chr1:10490063-10490113	MCF10A-Er-Src	breast:	n/a
19	chr1:10490063-10490113	GM12878	blood:	n/a
20	chr1:10490063-10490113	IMR90	lung:	fetal
21	chr1:10490063-10490113	HCF	heart:	n/a
22	chr1:10490063-10490113	SKMC	muscle:	n/a
23	chr1:10490063-10490113	T-47D	breast:	n/a
24	chr1:10490063-10490113	HRPEpiC	eye:	n/a
25	chr1:10490063-10490113	ovcar-3	ovarian:	n/a
26	chr1:10490063-10490113	SK-N-SH	brain:	n/a
27	chr1:10490063-10490113	NT2-D1	testis:	n/a
28	chr1:10490063-10490113	HIPEpiC	eye:	n/a
29	chr1:10490063-10490113	AoSMC	blood vessel:	n/a
30	chr1:10490063-10490113	ProgFib	skin:	n/a
31	chr1:10490063-10490113	LNCaP	prostate:	n/a
32	chr1:10490063-10490113	AG04449	skin:	fetal
33	chr1:10490063-10490113	HepG2	liver:	n/a
34	chr1:10490063-10490113	GM12892	blood:	n/a
35	chr1:10490063-10490113	AG09309	skin:	n/a
36	chr1:10490063-10490113	PrEC	prostate:	n/a
37	chr1:10490063-10490113	HRCEpiC	kidney:	n/a
38	chr1:10490063-10490113	HNPCEpiC	eye:	n/a
39	chr1:10490063-10490113	HCT-116	colon:	n/a
40	chr1:10490063-10490113	HL-60	blood:	n/a
41	chr1:10490063-10490113	AG09319	gingival:	n/a
42	chr1:10490063-10490113	NH-A	brain:	n/a
43	chr1:10490063-10490113	HAEpiC	amniotic membrane:	n/a
44	chr1:10490063-10490113	AG10803	skin:	n/a
45	chr1:10490063-10490113	AG04450	lung:	fetal
46	chr1:10490063-10490113	NHDF-neo	bronchial:	n/a
47	chr1:10490063-10490113	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:10490063-10490113	HUVEC	blood vessel:	n/a
49	chr1:10490063-10490113	K562	blood:	n/a
50	chr1:10490063-10490113	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:10475041..10475642-chr1:10489986..10490702,2	K562	blood:
2	chr1:10457794..10460664-chr1:10487844..10492697,5	K562	blood:
3	chr1:10488008..10492443-chr1:10531123..10534892,8	K562	blood:
4	chr1:10490085..10492364-chr1:10508772..10511442,3	K562	blood:
5	chr1:10488905..10491611-chr1:10518532..10520834,2	MCF-7	breast:
6	chr1:10489993..10493018-chr1:10531254..10535234,5	MCF-7	breast:
7	chr1:10489448..10493967-chr1:10494423..10498103,7	K562	blood:
8	chr1:10457794..10461321-chr1:10487053..10491931,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DFFA-1	chr1:10489938-10490734	ENSG00000271989.1

Variant related genes	Relation type
APITD1-CORT	TF binding region
APITD1	TF binding region
APITD1	CpG island
APITD1-CORT	CpG island
ENSG00000142655	Chromatin interaction
ENSG00000160049	Chromatin interaction
ENSG00000203469	Chromatin interaction
ENSG00000142657	Chromatin interaction
ENSG00000251503	Chromatin interaction
ENSG00000241563	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 4 )

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

rs_ID	r²[population]
rs10746494	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11121579	0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1203122	0.87[EUR][1000 genomes]
rs12565133	0.88[CEU][hapmap];0.95[CHB][hapmap];0.85[CHD][hapmap];0.84[GIH][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap]
rs1307485	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1307487	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1750349	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1760664	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2483679	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap]
rs2483684	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2781233	0.92[CEU][hapmap];0.81[CHD][hapmap];0.91[GIH][hapmap];0.82[JPT][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes]
rs36013615	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs475549	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs481571	0.93[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.96[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs491880	0.93[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs505141	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs517241	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs519472	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs520964	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs522029	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs522280	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs524150	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs528713	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs579398	0.93[ASN][1000 genomes]
rs583515	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs585703	0.96[ASN][1000 genomes]
rs586096	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs586223	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs597441	0.92[CEU][hapmap];0.89[GIH][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes]
rs628462	0.90[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs632690	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs634358	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs643400	0.89[EUR][1000 genomes]
rs649639	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs655271	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs666583	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs667366	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs670666	0.92[CEU][hapmap];0.95[CHB][hapmap];0.85[CHD][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];0.84[TSI][hapmap]
rs672606	0.86[EUR][1000 genomes]
rs673254	0.92[CEU][hapmap]
rs678850	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs681448	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs681495	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs684016	0.88[CEU][hapmap];0.80[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757722	chr1:10238070-10582554	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv2758920	chr1:10238070-10582554	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv817370	chr1:10305470-10697150	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1008021	chr1:10363794-10802633	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv2764192	chr1:10383734-10594186	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1003498	chr1:10445928-10607351	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription 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 miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv998731	chr1:10464176-10607351	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	esv3373675	chr1:10489565-10491863	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs649101	NPPA	cis	cerebellum	SCAN
rs649101	APITD1	cis	cerebellum	SCAN
rs649101	PLEKHG5	cis	parietal	SCAN
rs649101	KIAA2013	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10460000-10490200	Weak transcription	Psoas Muscle	Psoas
2	chr1:10479800-10490200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:10480200-10490400	Weak transcription	Aorta	Aorta
4	chr1:10480800-10490200	Weak transcription	Left Ventricle	heart
5	chr1:10481400-10490200	Weak transcription	Ovary	ovary
6	chr1:10482000-10490200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:10489800-10490200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:10489800-10490200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:10489800-10490200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:10489800-10490400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr1:10489800-10490400	Flanking Active TSS	Primary T cells from cord blood	blood
12	chr1:10489800-10490400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
13	chr1:10489800-10490400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:10489800-10490400	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr1:10489800-10490400	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr1:10489800-10490400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
17	chr1:10489800-10490400	Enhancers	Lung	lung
18	chr1:10489800-10490400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr1:10489800-10490400	Flanking Active TSS	Dnd41	blood
20	chr1:10489800-10490400	Flanking Active TSS	GM12878-XiMat	blood
21	chr1:10489800-10490400	Flanking Active TSS	Hela-S3	cervix
22	chr1:10489800-10490400	Flanking Active TSS	K562	blood
23	chr1:10489800-10491400	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr1:10489800-10491400	Active TSS	Brain Germinal Matrix	brain
25	chr1:10489800-10491600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:10489800-10491600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr1:10490000-10490200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:10490000-10490200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:10490000-10490200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:10490000-10490200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr1:10490000-10490200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr1:10490000-10490200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr1:10490000-10490200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr1:10490000-10490200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:10490000-10490200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:10490000-10490200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr1:10490000-10490200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:10490000-10490200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
39	chr1:10490000-10490200	Flanking Active TSS	Colon Smooth Muscle	Colon
40	chr1:10490000-10490200	Enhancers	Fetal Intestine Large	intestine
41	chr1:10490000-10490200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr1:10490000-10490200	Enhancers	Gastric	stomach
43	chr1:10490000-10490200	Flanking Active TSS	Right Atrium	heart
44	chr1:10490000-10490200	Enhancers	Right Ventricle	heart
45	chr1:10490000-10490200	Flanking Active TSS	Thymus	Thymus
46	chr1:10490000-10490200	Enhancers	Spleen	Spleen
47	chr1:10490000-10490200	Flanking Active TSS	A549	lung
48	chr1:10490000-10490400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
49	chr1:10490000-10490400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:10490000-10490400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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