Variant report

Variant	rs1419045
Chromosome Location	chr4:2937485-2937486
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:0)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBP	chr4:2937112-2938144	Hela-S3	cervix:	n/a	n/a
2	MAX	chr4:2936358-2937610	A549	lung:	n/a	n/a
3	POLR2A	chr4:2936416-2939933	GM18505	blood:	n/a	n/a
4	POLR2A	chr4:2936463-2940004	GM12891	blood:	n/a	n/a
5	SMC3	chr4:2936999-2938243	Hela-S3	cervix:	n/a	n/a
6	MAX	chr4:2936291-2937684	A549	lung:	n/a	n/a
7	POLR2A	chr4:2936427-2939614	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr4:2935540-2939822	Hela-S3	cervix:	n/a	n/a
9	MAX	chr4:2936301-2939648	HCT-116	colon:	n/a	n/a
10	YY1	chr4:2937461-2937703	K562	blood:	n/a	n/a
11	HCFC1	chr4:2936424-2938309	Hela-S3	cervix:	n/a	n/a
12	RELA	chr4:2937153-2939870	GM18505	blood:	n/a	n/a
13	MTA3	chr4:2936419-2940060	GM12878	blood:	n/a	n/a
14	POLR2A	chr4:2936420-2939905	K562	blood:	n/a	n/a
15	POLR2A	chr4:2936475-2940008	GM12891	blood:	n/a	n/a
16	POLR2A	chr4:2937124-2940033	K562	blood:	n/a	n/a
17	SIN3AK20	chr4:2936414-2939621	HCT-116	colon:	n/a	n/a
18	USF1	chr4:2937167-2937501	SK-N-SH_RA	brain:	n/a	n/a
19	WRNIP1	chr4:2937435-2937966	GM12878	blood:	n/a	n/a
20	POLR2A	chr4:2937075-2939631	H1-hESC	embryonic stem cell:	n/a	n/a
21	NFATC1	chr4:2936959-2939864	GM12878	blood:	n/a	n/a
22	JUND	chr4:2937092-2939655	HCT-116	colon:	n/a	n/a
23	NR2F2	chr4:2936909-2938256	K562	blood:	n/a	n/a
24	MAX	chr4:2937145-2937752	K562	blood:	n/a	n/a
25	POLR2A	chr4:2936428-2940062	K562	blood:	n/a	n/a
26	POLR2A	chr4:2936474-2938797	IMR90	lung:	n/a	n/a
27	POLR2A	chr4:2936942-2939390	SK-N-SH	brain:	n/a	n/a
28	HA-E2F1	chr4:2936657-2937802	MCF-7	breast:	n/a	n/a
29	POLR2A	chr4:2936392-2939634	HCT-116	colon:	n/a	n/a
30	POLR2A	chr4:2936273-2939674	MCF-7	breast:	n/a	n/a
31	ZNF263	chr4:2936629-2937899	HEK293-T-REx	kidney:	n/a	n/a
32	POLR2A	chr4:2936425-2939503	HCT-116	colon:	n/a	n/a
33	POLR2A	chr4:2936447-2940060	GM12892	blood:	n/a	n/a
34	NR2F2	chr4:2937218-2938099	K562	blood:	n/a	n/a
35	MAX	chr4:2936446-2938044	Hela-S3	cervix:	n/a	n/a
36	MXI1	chr4:2936462-2938347	GM12878	blood:	n/a	n/a
37	POLR2A	chr4:2936448-2937524	ECC-1	luminal epithelium:	n/a	n/a
38	RELA	chr4:2936499-2938801	GM12891	blood:	n/a	n/a
39	SMC3	chr4:2937065-2937801	GM12878	blood:	n/a	n/a
40	GTF2F1	chr4:2937407-2938144	Hela-S3	cervix:	n/a	n/a
41	MAX	chr4:2937369-2937509	HepG2	liver:	n/a	n/a
42	POLR2A	chr4:2936481-2939398	PBDE	blood:	n/a	n/a
43	POLR2A	chr4:2936416-2940081	GM12878	blood:	n/a	n/a
44	MAX	chr4:2936461-2937627	ECC-1	luminal epithelium:	n/a	n/a
45	MYC	chr4:2937183-2939811	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr4:2937058-2939858	K562	blood:	n/a	n/a
47	POLR2A	chr4:2936414-2940014	GM12878	blood:	n/a	n/a
48	POLR2A	chr4:2936327-2940084	HL-60	blood:	n/a	n/a
49	POLR2A	chr4:2937183-2939836	PANC-1	pancreas:	n/a	n/a
50	MAX	chr4:2937043-2937500	SK-N-SH	brain:	n/a	n/a

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2937223..2937791-chrX:15808121..15808824,2	Hela-S3	cervix:
2	chr4:2756410..2759745-chr4:2935120..2939466,6	K562	blood:
3	chr4:2830493..2833231-chr4:2936573..2940194,3	MCF-7	breast:
4	chr4:2903718..2915473-chr4:2930612..2941584,27	MCF-7	breast:
5	chr4:2795447..2803617-chr4:2934606..2939244,18	MCF-7	breast:
6	chr4:2818590..2823604-chr4:2934968..2940177,8	MCF-7	breast:
7	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:
8	chr4:2935808..2938115-chr4:3076304..3078834,3	K562	blood:
9	chr4:2744637..2750348-chr4:2934999..2939149,7	MCF-7	breast:
10	chr4:2866956..2870306-chr4:2932983..2937533,4	K562	blood:
11	chr1:149856723..149858846-chr4:2935922..2938266,2	MCF-7	breast:
12	chr4:2756586..2759605-chr4:2935863..2938872,4	K562	blood:
13	chr4:2936565..2939326-chr4:2970679..2973500,2	K562	blood:
14	chr4:2842030..2853279-chr4:2934021..2940851,24	MCF-7	breast:
15	chr4:2935142..2937747-chr4:2962615..2966345,4	MCF-7	breast:
16	chr4:2867681..2870567-chr4:2936383..2939288,2	MCF-7	breast:
17	chr4:2898532..2900285-chr4:2936066..2937849,2	MCF-7	breast:
18	chr4:2937332..2937943-chrX:41193378..41193993,2	Hela-S3	cervix:
19	chr4:2799331..2801814-chr4:2936733..2939693,2	K562	blood:
20	chr4:2936328..2940860-chr4:2961848..2966602,8	K562	blood:
21	chr4:774518..776312-chr4:2935741..2938166,2	MCF-7	breast:
22	chr4:2753882..2759883-chr4:2932429..2941474,15	MCF-7	breast:
23	chr4:2906552..2911481-chr4:2934891..2942965,11	MCF-7	breast:
24	chr4:2844179..2847079-chr4:2935598..2937938,4	MCF-7	breast:
25	chr18:3447926..3450158-chr4:2936583..2939331,2	MCF-7	breast:
26	chr4:2818330..2820965-chr4:2936129..2938646,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADD1-1	chr4:2937273-2939869	ENSG00000249673
2	lnc-ADD1-1	chr4:2937273-2938617	ENSG00000249673
3	lnc-ADD1-1	chr4:2937278-2939869	NR_015453
4	lnc-ADD1-1	chr4:2937273-2938617	ENSG00000249673.2

No data

Variant related genes	Relation type
NOP14-AS1	TF binding region
MFSD10	TF binding region
ENSG00000177426	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000087266	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000125388	Chromatin interaction
ENSG00000215301	Chromatin interaction
ENSG00000168884	Chromatin interaction
ENSG00000249592	Chromatin interaction
ENSG00000197386	Chromatin interaction
ENSG00000169249	Chromatin interaction
ENSG00000087274	Chromatin interaction
ENSG00000087269	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1012365	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1242228	0.86[CHB][hapmap]
rs1263338	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1263339	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1263342	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1263344	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1263345	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1263347	0.94[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1263349	1.00[CEU][hapmap];0.83[CHB][hapmap];0.81[CHD][hapmap];0.92[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1263360	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs12642795	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16843452	0.94[CEU][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];0.92[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs16843523	0.86[ASW][hapmap];0.89[CEU][hapmap];0.86[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.86[YRI][hapmap]
rs2051560	0.87[ASW][hapmap];1.00[CEU][hapmap];0.83[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.96[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2071695	1.00[CEU][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.92[EUR][1000 genomes]
rs2097081	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes]
rs2185885	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2237004	0.87[ASW][hapmap];0.94[CEU][hapmap];0.81[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.81[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2239728	0.87[ASW][hapmap];0.94[CEU][hapmap];0.87[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2282772	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2282773	0.92[EUR][1000 genomes]
rs2282774	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2285084	0.87[ASW][hapmap];0.94[CEU][hapmap];0.87[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2301374	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2857866	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3775068	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs3796469	0.94[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs4690000	0.89[CEU][hapmap]
rs4690001	0.89[CEU][hapmap];0.87[CHB][hapmap];0.89[CHD][hapmap];0.85[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap]
rs4690065	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4961	0.88[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4963	0.94[CEU][hapmap];0.86[JPT][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4964	0.87[ASW][hapmap];0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.94[MEX][hapmap];0.86[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73189458	0.90[EUR][1000 genomes]
rs762847	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs7664801	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats 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	63 gene(s)	inside rSNPs	diseases
3	nsv461163	chr4:2906285-3234980	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
4	nsv593437	chr4:2906285-3234980	Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	esv3440752	chr4:2934679-2937727	Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	esv3446681	chr4:2934779-2937527	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs1419045	HELT	trans	parietal	SCAN
rs1419045	ZNF732	cis	cerebellum	SCAN
rs1419045	ZFYVE28	cis	parietal	SCAN
rs1419045	DGKQ	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2934800-2937600	Active TSS	A549	lung
2	chr4:2935000-2937800	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr4:2935200-2938000	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr4:2935200-2938000	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr4:2935400-2937600	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr4:2935400-2937600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:2935400-2937600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:2935400-2937800	Active TSS	H9 Cell Line	embryonic stem cell
9	chr4:2935400-2938000	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr4:2935800-2937600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:2935800-2937600	Active TSS	GM12878-XiMat	blood
12	chr4:2936600-2937600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr4:2936600-2937600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:2936600-2937600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
15	chr4:2936600-2937600	Flanking Active TSS	Colonic Mucosa	Colon
16	chr4:2936600-2937600	Active TSS	Stomach Mucosa	stomach
17	chr4:2936600-2937800	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr4:2936600-2939600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
19	chr4:2936800-2937600	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr4:2936800-2937600	Flanking Active TSS	Pancreas	Pancrea
21	chr4:2936800-2937600	Flanking Active TSS	Stomach Smooth Muscle	stomach
22	chr4:2936800-2937800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:2936800-2937800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:2936800-2937800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr4:2936800-2937800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr4:2936800-2937800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr4:2936800-2938000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:2936800-2938400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
29	chr4:2936800-2939000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr4:2937000-2937600	Flanking Active TSS	Primary B cells from peripheral blood	blood
31	chr4:2937000-2937600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr4:2937000-2937600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr4:2937000-2937600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
34	chr4:2937000-2937600	Flanking Active TSS	Liver	Liver
35	chr4:2937000-2937600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr4:2937000-2937600	Flanking Active TSS	Brain Substantia Nigra	brain
37	chr4:2937000-2937600	Flanking Active TSS	Esophagus	oesophagus
38	chr4:2937000-2937600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr4:2937000-2937600	Flanking Active TSS	Fetal Muscle Trunk	muscle
40	chr4:2937000-2937600	Flanking Active TSS	Fetal Stomach	stomach
41	chr4:2937000-2937600	Flanking Active TSS	Fetal Thymus	thymus
42	chr4:2937000-2937600	Flanking Active TSS	Placenta Amnion	Placenta Amnion
43	chr4:2937000-2937600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr4:2937000-2937600	Flanking Active TSS	Right Ventricle	heart
45	chr4:2937000-2937600	Flanking Active TSS	HUVEC	blood vessel
46	chr4:2937000-2937600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr4:2937000-2937800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:2937000-2937800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:2937000-2937800	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr4:2937000-2937800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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