Variant report

Variant	rs2798851
Chromosome Location	chr1:144859929-144859930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:144859781-144860006	HepG2	liver:	n/a	n/a
2	CTCF	chr1:144859840-144859990	Hela-S3	cervix:	n/a	n/a
3	RAD21	chr1:144859831-144860008	GM12878	blood:	n/a	n/a
4	CTCF	chr1:144859800-144859950	HCM	heart:	n/a	n/a
5	CTCF	chr1:144859820-144859970	BJ	skin:	n/a	n/a
6	CTCF	chr1:144859820-144859970	GM12878	blood:	n/a	n/a
7	RAD21	chr1:144859841-144860033	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr1:144859800-144859950	BJ	skin:	n/a	n/a
9	CTCF	chr1:144859880-144860030	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr1:144859800-144859950	GM12875	blood:	n/a	n/a
11	CTCF	chr1:144859872-144860001	Hela-S3	cervix:	n/a	n/a
12	JUND	chr1:144859830-144859952	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr1:144859840-144859990	GM12870	blood:	n/a	n/a
14	CTCF	chr1:144859840-144859990	NB4	blood:	n/a	n/a
15	CHD2	chr1:144859804-144859990	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:144859824-144860026	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:144859860-144860010	GM12865	blood:	n/a	n/a
18	CTCF	chr1:144859880-144859996	K562	blood:	n/a	n/a
19	CTCF	chr1:144859780-144859930	AG09319	gingival:	n/a	n/a
20	EP300	chr1:144859686-144860069	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:144859860-144860010	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr1:144859820-144859970	GM12864	blood:	n/a	n/a
23	RAD21	chr1:144859603-144860188	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:144859800-144859950	GM12869	blood:	n/a	n/a
25	CTCF	chr1:144859860-144860010	GM12868	blood:	n/a	n/a
26	CTCF	chr1:144859860-144860010	GM12875	blood:	n/a	n/a
27	CTCF	chr1:144859880-144860030	GM12871	blood:	n/a	n/a
28	CTCF	chr1:144859728-144860076	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr1:144859860-144860010	K562	blood:	n/a	n/a
30	CTCF	chr1:144859860-144860010	GM12873	blood:	n/a	n/a
31	CTCF	chr1:144859883-144860020	GM12878	blood:	n/a	n/a
32	CTCF	chr1:144859840-144859990	HEK293	kidney:	n/a	n/a
33	CTCF	chr1:144859840-144859990	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr1:144859840-144859990	NHEK	skin:	n/a	n/a
35	CTCF	chr1:144859860-144860010	HCFaa	heart:	n/a	n/a
36	CTCF	chr1:144859820-144859970	HCT-116	colon:	n/a	n/a
37	CTCF	chr1:144859860-144860010	GM12878	blood:	n/a	n/a
38	CTCF	chr1:144859860-144860010	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr1:144859818-144860050	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:144859860-144860010	GM12866	blood:	n/a	n/a
41	CTCF	chr1:144859869-144860005	HepG2	liver:	n/a	n/a
42	CTCF	chr1:144859683-144860136	H1-hESC	embryonic stem cell:	n/a	n/a
43	RAD21	chr1:144859675-144860214	HCT-116	colon:	n/a	n/a
44	ZNF143	chr1:144859760-144860049	H1-hESC	embryonic stem cell:	n/a	n/a
45	RAD21	chr1:144859704-144860074	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr1:144859760-144860009	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr1:144859778-144860216	MCF-7	breast:	n/a	n/a
48	SP1	chr1:144859668-144860060	H1-hESC	embryonic stem cell:	n/a	chr1:144859816-144859827
49	SMC3	chr1:144859862-144860026	GM12878	blood:	n/a	n/a
50	CTCF	chr1:144859860-144860010	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144859929-144859979	SK-N-SH	brain:	n/a
2	chr1:144859929-144859979	GM12892	blood:	n/a
3	chr1:144859929-144859979	HCM	heart:	n/a
4	chr1:144859929-144859979	Caco-2	colon:	n/a
5	chr1:144859929-144859979	GM06990	blood:	n/a
6	chr1:144859929-144859979	SKMC	muscle:	n/a
7	chr1:144859929-144859979	HL-60	blood:	n/a
8	chr1:144859929-144859979	AG09309	skin:	n/a
9	chr1:144859929-144859979	IMR90	lung:	fetal
10	chr1:144859929-144859979	ECC-1	luminal epithelium:	n/a
11	chr1:144859929-144859979	H1-hESC	embryonic stem cell:	embryo
12	chr1:144859929-144859979	HRPEpiC	eye:	n/a
13	chr1:144859929-144859979	HEK293	kidney:	embryo
14	chr1:144859929-144859979	HepG2	liver:	n/a
15	chr1:144859929-144859979	HCT-116	colon:	n/a
16	chr1:144859929-144859979	Hepatocyte	liver:	n/a
17	chr1:144859929-144859979	AG10803	skin:	n/a
18	chr1:144859929-144859979	SK-N-MC	brain:	n/a
19	chr1:144859929-144859979	HAEpiC	amniotic membrane:	n/a
20	chr1:144859929-144859979	NT2-D1	testis:	n/a
21	chr1:144859929-144859979	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:144859929-144859979	K562	blood:	n/a
23	chr1:144859929-144859979	ovcar-3	ovarian:	n/a
24	chr1:144859929-144859979	CMK	blood:	n/a
25	chr1:144859929-144859979	AG04450	lung:	fetal
26	chr1:144859929-144859979	HCF	heart:	n/a
27	chr1:144859929-144859979	HEEpiC	esophagus:	n/a
28	chr1:144859929-144859979	NH-A	brain:	n/a
29	chr1:144859929-144859979	RPTEC	kidney:	n/a
30	chr1:144859929-144859979	HRE	kidney:	n/a
31	chr1:144859929-144859979	PANC-1	pancreas:	n/a
32	chr1:144859929-144859979	BJ	skin:	n/a
33	chr1:144859929-144859979	SK-N-SH_RA	brain:	n/a
34	chr1:144859929-144859979	NHBE	bronchial:	n/a
35	chr1:144859929-144859979	T-47D	breast:	n/a
36	chr1:144859929-144859979	ProgFib	skin:	n/a
37	chr1:144859929-144859979	MCF10A-Er-Src	breast:	n/a
38	chr1:144859929-144859979	AG04449	skin:	fetal
39	chr1:144859929-144859979	GM12878	blood:	n/a
40	chr1:144859929-144859979	Jurkat	blood:	n/a
41	chr1:144859929-144859979	GM19239	blood:	n/a
42	chr1:144859929-144859979	PrEC	prostate:	n/a
43	chr1:144859929-144859979	A549	lung:	n/a
44	chr1:144859929-144859979	HUVEC	blood vessel:	n/a
45	chr1:144859929-144859979	AoSMC	blood vessel:	n/a
46	chr1:144859929-144859979	HRCEpiC	kidney:	n/a
47	chr1:144859929-144859979	HMEC	breast:	n/a
48	chr1:144859929-144859979	NB4	blood:	n/a
49	chr1:144859929-144859979	MCF-7	breast:	n/a
50	chr1:144859929-144859979	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:144858012..144861709-chr1:144865100..144867014,3	K562	blood:
2	chr1:144858037..144860054-chr1:144867098..144869572,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPIAL4B-6	chr1:144859759-144860234	NONHSAT005854

No data

Variant related genes	Relation type
PDE4DIP	TF binding region
PDE4DIP	CpG island
ENSG00000178104	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1343471	1.00[EUR][1000 genomes]
rs1698597	1.00[EUR][1000 genomes]
rs1747899	1.00[EUR][1000 genomes]
rs1778104	1.00[EUR][1000 genomes]
rs1778121	1.00[EUR][1000 genomes]
rs2653678	1.00[EUR][1000 genomes]
rs2653711	1.00[EUR][1000 genomes]
rs2798889	1.00[EUR][1000 genomes]
rs2798894	1.00[EUR][1000 genomes]
rs2798904	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3795671	1.00[EUR][1000 genomes]
rs719603	1.00[EUR][1000 genomes]

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	nsv1001989	chr1:144007818-144873327	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
2	nsv997949	chr1:144007818-144876884	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
3	nsv1010670	chr1:144007818-144880405	Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
4	nsv1010163	chr1:144007818-144884322	Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	265 gene(s)	inside rSNPs	diseases
5	nsv1014985	chr1:144007818-144949963	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
6	esv1828275	chr1:144274482-145098718	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer 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 miRNA target site	304 gene(s)	inside rSNPs	diseases
7	nsv1014641	chr1:144337917-144880405	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
8	nsv998833	chr1:144337917-144885032	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
9	nsv1009682	chr1:144471974-144876884	Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking 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	255 gene(s)	inside rSNPs	diseases
10	nsv1008142	chr1:144471974-144880405	Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
11	nsv1001693	chr1:144471974-145290292	Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	311 gene(s)	inside rSNPs	diseases
12	nsv872206	chr1:144544101-144881389	Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
13	nsv872208	chr1:144560355-144875799	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
14	nsv872209	chr1:144600291-144881389	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv872210	chr1:144617179-144924792	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
16	esv3359519	chr1:144674517-144950252	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS 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	33 gene(s)	inside rSNPs	diseases
17	esv3493993	chr1:144674667-144950191	Strong transcription ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
18	esv3493994	chr1:144674667-144950191	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
19	esv1830469	chr1:144679113-145320996	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
20	nsv436611	chr1:144709882-144978624	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking 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 miRNA target site	32 gene(s)	inside rSNPs	diseases
21	nsv435736	chr1:144709964-144987027	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	esv18675	chr1:144810749-144882876	Genic enhancers ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
23	nsv946244	chr1:144811539-144897508	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
24	nsv831315	chr1:144813808-144962476	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
25	nsv872211	chr1:144828599-144894697	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
26	esv2761854	chr1:144832255-144921857	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
27	esv2630464	chr1:144841079-144893666	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
28	nsv872212	chr1:144850451-145073750	Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
29	esv21270	chr1:144851761-144876388	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144821400-144865000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:144824600-144863400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:144826600-144860000	Weak transcription	Fetal Kidney	kidney
4	chr1:144841600-144861800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:144843800-144864800	Weak transcription	Fetal Lung	lung
6	chr1:144843800-144865000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr1:144843800-144880600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:144849800-144871600	Strong transcription	Skeletal Muscle Male	skeletal muscle
9	chr1:144850000-144860400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:144850000-144860400	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr1:144850000-144860600	Strong transcription	Left Ventricle	heart
12	chr1:144850000-144860600	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr1:144850000-144865600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr1:144850000-144865800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:144850000-144868800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:144850000-144870400	Strong transcription	Skeletal Muscle Female	skeletal muscle
17	chr1:144850000-144874000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr1:144850000-144875800	Strong transcription	Liver	Liver
19	chr1:144850000-144883200	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr1:144850000-144883600	Strong transcription	Duodenum Mucosa	Duodenum
21	chr1:144850000-144883800	Strong transcription	Muscle Satellite Cultured Cells	--
22	chr1:144850000-144885800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:144850000-144886200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:144850000-144886200	Strong transcription	Osteobl	bone
25	chr1:144850000-144886400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr1:144850000-144894000	Strong transcription	Stomach Smooth Muscle	stomach
27	chr1:144850200-144860400	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr1:144850200-144860400	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr1:144850400-144883400	Strong transcription	Fetal Brain Female	brain
30	chr1:144850400-144886200	Strong transcription	HSMMtube	muscle
31	chr1:144850400-144886600	Strong transcription	Adipose Nuclei	Adipose
32	chr1:144850400-144894200	Strong transcription	Brain Germinal Matrix	brain
33	chr1:144851200-144884400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:144851600-144860200	Strong transcription	Fetal Stomach	stomach
35	chr1:144851600-144860600	Strong transcription	Aorta	Aorta
36	chr1:144851600-144884000	Strong transcription	Placenta	Placenta
37	chr1:144852200-144913200	Weak transcription	Stomach Mucosa	stomach
38	chr1:144852600-144860200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:144852600-144860400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr1:144853800-144860400	Strong transcription	Rectal Smooth Muscle	rectum
41	chr1:144854000-144865200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr1:144854000-144867800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:144854200-144870200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:144854200-144886000	Weak transcription	Right Atrium	heart
45	chr1:144854400-144860200	Strong transcription	Ovary	ovary
46	chr1:144854800-144865200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr1:144855000-144860400	Strong transcription	Fetal Intestine Large	intestine
48	chr1:144855200-144860200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:144855400-144862800	Strong transcription	Psoas Muscle	Psoas
50	chr1:144855800-144860400	Strong transcription	Primary T cells from cord blood	blood

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