Variant report

Variant	rs2655794
Chromosome Location	chr1:144534635-144534636
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:113)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:144533879..144534865-chr5:77071427..77072208,2	Hela-S3	cervix:
2	chr1:144534225..144536279-chr2:5765333..5766332,12	MCF-7	breast:
3	chr1:144526974..144536279-chr1:149221211..149226185,98	K562	blood:
4	chr1:144533498..144535527-chr14:56140284..56141806,2	K562	blood:
5	chr1:144530771..144535863-chr1:144988447..145007040,21	K562	blood:
6	chr1:144533798..144534678-chr6:33239455..33240159,2	Hela-S3	cervix:
7	chr1:144534120..144534744-chr11:62648041..62648567,2	Hela-S3	cervix:
8	chr1:144533858..144534676-chr5:137800598..137801362,2	HCT-116	colon:
9	chr1:144534046..144534703-chr8:119123617..119124191,2	Hela-S3	cervix:
10	chr1:144533721..144534707-chr20:1305699..1306434,2	Hela-S3	cervix:
11	chr1:144533804..144534642-chrX:77359329..77359942,2	Hela-S3	cervix:
12	chr1:45187271..45188987-chr1:144532926..144535604,2	K562	blood:
13	chr1:144533848..144534656-chr15:51057553..51058077,2	Hela-S3	cervix:
14	chr1:144533945..144534883-chr3:133292589..133293471,2	Hela-S3	cervix:
15	chr1:144534120..144534711-chr12:12870119..12870939,2	Hela-S3	cervix:
16	chr1:144533638..144534730-chr2:88315452..88316503,4	Hela-S3	cervix:
17	chr1:144534155..144534665-chr1:150551597..150552482,2	Hela-S3	cervix:
18	chr1:144533892..144534669-chr7:65958197..65958873,2	Hela-S3	cervix:
19	chr1:144534065..144535931-chr1:145036199..145038965,3	K562	blood:
20	chr1:144533842..144534691-chr2:136633807..136634701,2	Hela-S3	cervix:
21	chr1:144534120..144534663-chr12:8185207..8185847,2	Hela-S3	cervix:
22	chr1:144533735..144534707-chr3:52187701..52188643,2	Hela-S3	cervix:
23	chr1:144532709..144537146-chr1:146553385..146558827,17	K562	blood:
24	chr1:144534213..144536284-chr1:145054889..145056789,2	MCF-7	breast:
25	chr1:144527325..144537192-chr1:149221188..149227183,106	K562	blood:
26	chr1:36235021..36235536-chr1:144534159..144534971,2	Hela-S3	cervix:
27	chr1:144534122..144534747-chr11:70049000..70049903,2	Hela-S3	cervix:
28	chr1:144532854..144535765-chr1:148603401..148605214,4	K562	blood:
29	chr1:144529973..144534952-chr1:149221200..149225268,6	MCF-7	breast:
30	chr1:144526732..144539178-chr1:149221186..149225476,28	MCF-7	breast:
31	chr1:144533861..144534724-chr7:130791151..130791980,2	Hela-S3	cervix:
32	chr1:144534039..144536275-chr2:121126928..121129908,2	K562	blood:
33	chr1:144534227..144534761-chr6:86353322..86354100,2	Hela-S3	cervix:
34	chr1:120428374..120430929-chr1:144532739..144535945,3	K562	blood:
35	chr1:144534224..144534761-chr17:39845113..39845806,2	Hela-S3	cervix:
36	chr1:144533744..144537008-chr1:149856854..149861459,6	K562	blood:
37	chr1:144534089..144535693-chr1:145093143..145095512,2	K562	blood:
38	chr1:17229738..17236634-chr1:144531729..144537089,21	K562	blood:
39	chr1:144532329..144535680-chr1:145012343..145016063,5	K562	blood:
40	chr1:144533872..144534647-chr17:62206901..62207643,2	Hela-S3	cervix:
41	chr1:144533809..144535358-chr1:149604555..149606316,2	K562	blood:
42	chr1:144532746..144535679-chr1:148240132..148243070,2	K562	blood:
43	chr1:144533839..144534637-chr9:130374190..130374874,2	Hela-S3	cervix:
44	chr1:144534165..144535123-chr19:16186001..16186846,2	Hela-S3	cervix:
45	chr1:144533960..144534647-chr17:16342053..16342570,2	Hela-S3	cervix:
46	chr1:144533737..144534794-chr20:47537863..47538708,3	Hela-S3	cervix:
47	chr1:144531278..144537146-chr1:146553717..146557612,11	K562	blood:
48	chr1:144533804..144534765-chr16:31884832..31885496,2	Hela-S3	cervix:
49	chr1:144532673..144535225-chr1:149604575..149607265,3	K562	blood:
50	chr1:144534129..144534996-chr2:5764850..5765853,7	HCT-116	colon:

No data

Variant related genes	Relation type
ENSG00000231721	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000236943	Chromatin interaction
ENSG00000102144	Chromatin interaction
ENSG00000272755	Chromatin interaction
ENSG00000133398	Chromatin interaction
ENSG00000202408	Chromatin interaction
ENSG00000111276	Chromatin interaction
ENSG00000270141	Chromatin interaction
ENSG00000207205	Chromatin interaction
ENSG00000223473	Chromatin interaction
ENSG00000182197	Chromatin interaction
ENSG00000237310	Chromatin interaction
ENSG00000113580	Chromatin interaction
ENSG00000252826	Chromatin interaction
ENSG00000236200	Chromatin interaction
ENSG00000175061	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000153208	Chromatin interaction
ENSG00000147123	Chromatin interaction
ENSG00000120093	Chromatin interaction
ENSG00000207349	Chromatin interaction
ENSG00000138085	Chromatin interaction
ENSG00000272426	Chromatin interaction
ENSG00000178607	Chromatin interaction
ENSG00000268172	Chromatin interaction
ENSG00000169189	Chromatin interaction
ENSG00000076003	Chromatin interaction
ENSG00000245888	Chromatin interaction
ENSG00000223501	Chromatin interaction
ENSG00000222724	Chromatin interaction
ENSG00000185947	Chromatin interaction
ENSG00000083838	Chromatin interaction
ENSG00000272993	Chromatin interaction
ENSG00000007968	Chromatin interaction
ENSG00000170633	Chromatin interaction
ENSG00000126777	Chromatin interaction
ENSG00000171530	Chromatin interaction
ENSG00000206737	Chromatin interaction
ENSG00000196204	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000252656	Chromatin interaction
ENSG00000181991	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000168040	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000115073	Chromatin interaction
ENSG00000063177	Chromatin interaction
ENSG00000207501	Chromatin interaction
ENSG00000182872	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000138600	Chromatin interaction
ENSG00000202496	Chromatin interaction
ENSG00000231500	Chromatin interaction
ENSG00000079999	Chromatin interaction
ENSG00000234684	Chromatin interaction
ENSG00000124193	Chromatin interaction
ENSG00000167460	Chromatin interaction
ENSG00000173812	Chromatin interaction
ENSG00000089053	Chromatin interaction
ENSG00000185825	Chromatin interaction
ENSG00000091527	Chromatin interaction
ENSG00000168003	Chromatin interaction
ENSG00000226446	Chromatin interaction
ENSG00000129810	Chromatin interaction
ENSG00000243452	Chromatin interaction
ENSG00000100227	Chromatin interaction
ENSG00000270022	Chromatin interaction
ENSG00000136854	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000184277	Chromatin interaction
ENSG00000269501	Chromatin interaction
ENSG00000176619	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000117054	Chromatin interaction
ENSG00000125775	Chromatin interaction
ENSG00000124198	Chromatin interaction
ENSG00000230832	Chromatin interaction
ENSG00000178104	Chromatin interaction
ENSG00000120306	Chromatin interaction
ENSG00000232151	Chromatin interaction
ENSG00000164087	Chromatin interaction
ENSG00000120738	Chromatin interaction
ENSG00000065970	Chromatin interaction
ENSG00000108511	Chromatin interaction
ENSG00000135316	Chromatin interaction
ENSG00000138074	Chromatin interaction
ENSG00000092853	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10737112	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs12130335	0.82[AMR][1000 genomes]
rs17161431	0.82[AMR][1000 genomes]
rs2455992	0.91[AMR][1000 genomes]
rs2655742	0.84[AMR][1000 genomes]
rs2655793	0.91[AMR][1000 genomes]
rs28663124	0.91[AMR][1000 genomes]
rs2938632	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2940060	0.91[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003583	chr1:144007818-144543442	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
2	nsv1002681	chr1:144007818-144560590	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
3	nsv1012104	chr1:144007818-144682096	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	260 gene(s)	inside rSNPs	diseases
4	nsv1006330	chr1:144007818-144849544	Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	262 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	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
9	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
10	nsv1002373	chr1:144013582-144682096	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	258 gene(s)	inside rSNPs	diseases
11	nsv1007748	chr1:144015838-144682096	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	258 gene(s)	inside rSNPs	diseases
12	nsv997876	chr1:144033939-144538748	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
13	nsv524682	chr1:144034888-144617179	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
14	nsv1007246	chr1:144036737-144560590	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
15	nsv1006612	chr1:144050098-144560590	Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
16	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
17	esv2512286	chr1:144321887-144560360	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	251 gene(s)	inside rSNPs	diseases
18	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
19	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
20	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
21	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
22	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
23	nsv831292	chr1:144506093-144613511	Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS 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	248 gene(s)	inside rSNPs	diseases
24	nsv831303	chr1:144523643-144617215	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	248 gene(s)	inside rSNPs	diseases
25	nsv946237	chr1:144533425-144535801	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	246 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144532800-144534800	ZNF genes & repeats	Right Atrium	heart
2	chr1:144533600-144535000	Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr1:144533600-144535000	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr1:144533600-144535000	Active TSS	A549	lung
5	chr1:144533800-144535000	Active TSS	K562	blood
6	chr1:144534000-144537400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:144534200-144535000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:144534200-144537400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:144534200-144537600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:144534400-144535000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr1:144534400-144535000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr1:144534400-144535000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:144534400-144535000	Weak transcription	HSMM	muscle
14	chr1:144534400-144535000	Weak transcription	NHDF-Ad	bronchial
15	chr1:144534400-144535200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:144534400-144535200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:144534400-144535200	Bivalent Enhancer	Primary T cells from cord blood	blood
18	chr1:144534400-144535200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:144534400-144535200	Weak transcription	Lung	lung
20	chr1:144534400-144535200	Weak transcription	Psoas Muscle	Psoas
21	chr1:144534400-144535200	Weak transcription	Thymus	Thymus
22	chr1:144534400-144535200	Enhancers	GM12878-XiMat	blood
23	chr1:144534400-144535200	Weak transcription	NH-A	brain
24	chr1:144534400-144535400	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr1:144534400-144535600	Enhancers	Fetal Muscle Trunk	muscle
26	chr1:144534400-144535800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr1:144534400-144536000	Enhancers	Primary T cells fromperipheralblood	blood
28	chr1:144534400-144536000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr1:144534400-144536000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr1:144534400-144536000	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr1:144534400-144536600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:144534400-144536600	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr1:144534400-144536800	Enhancers	Primary B cells from peripheral blood	blood
34	chr1:144534400-144537200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:144534400-144537200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr1:144534400-144537200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr1:144534400-144537200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr1:144534400-144537200	Weak transcription	Gastric	stomach
39	chr1:144534400-144537200	Weak transcription	Pancreas	Pancrea
40	chr1:144534400-144537400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr1:144534400-144537400	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr1:144534400-144537400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:144534400-144537600	Weak transcription	Colonic Mucosa	Colon
44	chr1:144534400-144537800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr1:144534400-144539400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:144534400-144539400	Weak transcription	Right Ventricle	heart
47	chr1:144534400-144540400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr1:144534600-144534800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr1:144534600-144534800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr1:144534600-144534800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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