Variant report

Variant	esv34666
Chromosome Location	chr12:34374879-34760333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1511)
CpG islands
(count:9776)
Chromatin interactive
region (count:35)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1511 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:34417095-34417295	K562	blood:	n/a	n/a
2	ATF1	chr12:34407159-34407233	K562	blood:	n/a	n/a
3	ATF1	chr12:34430831-34430993	K562	blood:	n/a	n/a
4	ATF3	chr12:34509237-34509520	K562	blood:	n/a	n/a
5	ATF3	chr12:34509280-34509455	K562	blood:	n/a	n/a
6	BACH1	chr12:34428886-34428914	K562	blood:	n/a	n/a
7	BACH1	chr12:34486593-34486711	K562	blood:	n/a	n/a
8	BACH1	chr12:34429857-34430227	K562	blood:	n/a	n/a
9	BACH1	chr12:34500299-34500489	K562	blood:	n/a	n/a
10	BACH1	chr12:34417965-34418172	K562	blood:	n/a	n/a
11	BACH1	chr12:34489607-34489683	K562	blood:	n/a	n/a
12	BACH1	chr12:34429537-34429559	K562	blood:	n/a	n/a
13	BACH1	chr12:34417075-34417361	K562	blood:	n/a	n/a
14	BATF	chr12:34575360-34575508	GM12878	blood:	n/a	n/a
15	BATF	chr12:34575259-34575544	GM12878	blood:	n/a	n/a
16	BATF	chr12:34374801-34375081	GM12878	blood:	n/a	n/a
17	BATF	chr12:34387277-34387522	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:34575348-34575583	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:34575364-34575543	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:34575344-34575524	HepG2	liver:	n/a	n/a
21	BHLHE40	chr12:34500243-34500651	K562	blood:	n/a	chr12:34500434-34500450
22	BHLHE40	chr12:34428714-34428914	K562	blood:	n/a	n/a
23	BHLHE40	chr12:34501989-34502240	K562	blood:	n/a	n/a
24	BHLHE40	chr12:34509153-34509543	K562	blood:	n/a	n/a
25	BHLHE40	chr12:34645482-34645650	HepG2	liver:	n/a	n/a
26	BHLHE40	chr12:34503265-34503867	K562	blood:	n/a	chr12:34503364-34503380
27	BHLHE40	chr12:34489695-34490283	K562	blood:	n/a	chr12:34490108-34490124
28	BHLHE40	chr12:34484701-34484766	K562	blood:	n/a	n/a
29	BHLHE40	chr12:34417073-34417446	K562	blood:	n/a	n/a
30	BHLHE40	chr12:34499722-34499980	K562	blood:	n/a	n/a
31	BHLHE40	chr12:34488959-34488987	K562	blood:	n/a	n/a
32	BHLHE40	chr12:34417796-34417999	K562	blood:	n/a	n/a
33	BHLHE40	chr12:34501108-34501225	K562	blood:	n/a	n/a
34	BHLHE40	chr12:34429855-34430232	K562	blood:	n/a	n/a
35	BHLHE40	chr12:34499008-34499021	K562	blood:	n/a	n/a
36	BHLHE40	chr12:34544817-34545121	K562	blood:	n/a	n/a
37	BHLHE40	chr12:34494224-34494316	K562	blood:	n/a	n/a
38	BRCA1	chr12:34429859-34430235	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr12:34516242-34516252	HepG2	liver:	n/a	n/a
40	BRCA1	chr12:34417803-34417997	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr12:34429536-34429561	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr12:34417797-34418168	GM12878	blood:	n/a	n/a
43	BRCA1	chr12:34429446-34429561	GM12878	blood:	n/a	n/a
44	BRCA1	chr12:34417092-34417445	GM12878	blood:	n/a	n/a
45	BRCA1	chr12:34429856-34430234	GM12878	blood:	n/a	n/a
46	CBX3	chr12:34438038-34438225	K562	blood:	n/a	n/a
47	CBX3	chr12:34503332-34503995	K562	blood:	n/a	n/a
48	CBX3	chr12:34560747-34561019	K562	blood:	n/a	n/a
49	CBX3	chr12:34488602-34489199	K562	blood:	n/a	n/a
50	CBX3	chr12:34499643-34499985	K562	blood:	n/a	n/a

(count:9776 , 50 per page) page: 1 2 3 4 5 6 7 ... 196

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34481883-34481933	HEK293	kidney:	embryo
2	chr12:34556603-34556653	NB4	blood:	n/a
3	chr12:34478388-34478438	BE2_C	brain:	n/a
4	chr12:34503176-34503226	HRCEpiC	kidney:	n/a
5	chr12:34534365-34534415	HAEpiC	amniotic membrane:	n/a
6	chr12:34474362-34474412	T-47D	breast:	n/a
7	chr12:34453757-34453807	AG04450	lung:	fetal
8	chr12:34755568-34755618	HUVEC	blood vessel:	n/a
9	chr12:34489995-34490045	AoSMC	blood vessel:	n/a
10	chr12:34491142-34491192	HRCEpiC	kidney:	n/a
11	chr12:34500813-34500863	SK-N-SH_RA	brain:	n/a
12	chr12:34480428-34480478	GM19239	blood:	n/a
13	chr12:34446650-34446700	AG09319	gingival:	n/a
14	chr12:34755568-34755618	HEEpiC	esophagus:	n/a
15	chr12:34506462-34506512	GM12892	blood:	n/a
16	chr12:34498372-34498422	GM12878	blood:	n/a
17	chr12:34481883-34481933	HEK293	kidney:	embryo
18	chr12:34556603-34556653	NB4	blood:	n/a
19	chr12:34478388-34478438	BE2_C	brain:	n/a
20	chr12:34503176-34503226	HRCEpiC	kidney:	n/a
21	chr12:34534365-34534415	HAEpiC	amniotic membrane:	n/a
22	chr12:34474362-34474412	T-47D	breast:	n/a
23	chr12:34453757-34453807	AG04450	lung:	fetal
24	chr12:34755568-34755618	HUVEC	blood vessel:	n/a
25	chr12:34489995-34490045	AoSMC	blood vessel:	n/a
26	chr12:34491142-34491192	HRCEpiC	kidney:	n/a
27	chr12:34500813-34500863	SK-N-SH_RA	brain:	n/a
28	chr12:34480428-34480478	GM19239	blood:	n/a
29	chr12:34446650-34446700	AG09319	gingival:	n/a
30	chr12:34755568-34755618	HEEpiC	esophagus:	n/a
31	chr12:34506462-34506512	GM12892	blood:	n/a
32	chr12:34498372-34498422	GM12878	blood:	n/a
33	chr12:34478695-34478745	BE2_C	brain:	n/a
34	chr12:34480142-34480192	AoSMC	blood vessel:	n/a
35	chr12:34457254-34457304	RPTEC	kidney:	n/a
36	chr12:34511886-34511936	ECC-1	luminal epithelium:	n/a
37	chr12:34554116-34554166	GM12891	blood:	n/a
38	chr12:34546775-34546825	HCM	heart:	n/a
39	chr12:34523825-34523875	AG10803	skin:	n/a
40	chr12:34481804-34481854	GM12892	blood:	n/a
41	chr12:34522534-34522584	AG09309	skin:	n/a
42	chr12:34547604-34547654	GM19239	blood:	n/a
43	chr12:34491142-34491192	Hepatocyte	liver:	n/a
44	chr12:34530380-34530430	HEEpiC	esophagus:	n/a
45	chr12:34554116-34554166	HRCEpiC	kidney:	n/a
46	chr12:34511504-34511554	PFSK-1	brain:	n/a
47	chr12:34756291-34756341	HEEpiC	esophagus:	n/a
48	chr12:34480221-34480271	PrEC	prostate:	n/a
49	chr12:34457912-34457962	HepG2	liver:	n/a
50	chr12:34487126-34487176	Jurkat	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:34500138..34502153-chr12:34504147..34506890,2	K562	blood:
2	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
3	chr12:34472451..34474607-chr12:34482688..34484610,2	K562	blood:
4	chr12:34542219..34546005-chr12:34547286..34550175,4	K562	blood:
5	chr12:34544160..34546005-chr12:34547460..34549884,2	K562	blood:
6	chr12:34416477..34418281-chr16:33956682..33958772,3	MCF-7	breast:
7	chr12:34500138..34502153-chr12:34504147..34506890,2	K562	blood:
8	chr12:34497129..34499259-chr12:34508235..34509796,2	K562	blood:
9	chr12:34480099..34482680-chr12:34485043..34486658,2	K562	blood:
10	chr12:34497467..34501951-chr12:34506676..34509735,4	K562	blood:
11	chr12:34501359..34504154-chr12:34510668..34513544,2	K562	blood:
12	chr12:34376481..34379453-chr12:34384361..34386376,2	K562	blood:
13	chr12:34497610..34503522-chr12:34523490..34528831,5	K562	blood:
14	chr12:34279057..34280887-chr12:34440053..34441876,2	K562	blood:
15	chr12:34427757..34428277-chr16:33958747..33959470,2	MCF-7	breast:
16	chr12:34544160..34546005-chr12:34547460..34549884,2	K562	blood:
17	chr12:34542219..34546005-chr12:34547286..34550175,4	K562	blood:
18	chr12:34416748..34417268-chr2:133025884..133026405,2	MCF-7	breast:
19	chr12:34480099..34482680-chr12:34485043..34486658,2	K562	blood:
20	chr12:34543477..34545374-chr12:34550348..34552407,2	K562	blood:
21	chr12:34376481..34379453-chr12:34384361..34386376,2	K562	blood:
22	chr12:34513093..34516192-chr12:34527570..34530403,3	K562	blood:
23	chr12:34472451..34474607-chr12:34482688..34484610,2	K562	blood:
24	chr12:34405769..34407368-chr12:38464924..38466718,2	K562	blood:
25	chr12:34497610..34503522-chr12:34523490..34528831,5	K562	blood:
26	chr12:34497467..34501951-chr12:34506676..34509735,4	K562	blood:
27	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:
28	chr12:34497129..34499259-chr12:34508235..34509796,2	K562	blood:
29	chr12:34491491..34493706-chr12:34544208..34545803,2	K562	blood:
30	chr12:34513093..34516192-chr12:34527570..34530403,3	K562	blood:
31	chr12:34487742..34489883-chr12:34492282..34495193,2	K562	blood:
32	chr12:34501359..34504154-chr12:34510668..34513544,2	K562	blood:
33	chr12:34543477..34545374-chr12:34550348..34552407,2	K562	blood:
34	chr12:34487742..34489883-chr12:34492282..34495193,2	K562	blood:
35	chr12:34491491..34493706-chr12:34544208..34545803,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-4	chr12:34402416-34402893	NONHSAT140067
2	lnc-ALG10-5	chr12:34421984-34422141	NONHSAT027661
3	lnc-ALG10-5	chr12:34430929-34431017	NONHSAT027661

No data

Variant related genes	Relation type
ENSG00000255652	TF binding region
ENSG00000256614	TF binding region
ENSG00000255652	CpG island
ENSG00000256614	CpG island

Extended variants
information (count: 21583 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:21583 , 50 per page) page: 1 2 3 4 5 6 7 ... 432

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7961508	chr12:34374879-34374880	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138764870	chr12:34374880-34374881	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs557171755	chr12:34374899-34374900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs575696930	chr12:34374939-34374940	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs550057631	chr12:34374947-34374948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs551969596	chr12:34374958-34374959	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs189914182	chr12:34374981-34374982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs561996421	chr12:34374995-34374996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534334323	chr12:34375003-34375004	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs376516056	chr12:34375021-34375022	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs34781558	chr12:34375058-34375059	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs138081643	chr12:34375063-34375064	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs549839776	chr12:34375930-34375931	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs74073574	chr12:34375933-34375934	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs112089223	chr12:34376154-34376155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs111553995	chr12:34376158-34376159	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs147708277	chr12:34376178-34376179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs117234245	chr12:34376439-34376440	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573735989	chr12:34382637-34382638	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs187571951	chr12:34382641-34382642	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs562478955	chr12:34382714-34382715	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs541109159	chr12:34382719-34382720	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs11358455	chr12:34382720-34382721	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs397697007	chr12:34382734-34382735	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs74073581	chr12:34382748-34382749	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs182565083	chr12:34382770-34382771	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs188030390	chr12:34382790-34382791	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs547527218	chr12:34382809-34382810	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs544484182	chr12:34382888-34382889	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs530104884	chr12:34382941-34382942	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs557998727	chr12:34382978-34382979	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs372836385	chr12:34383058-34383059	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs549921720	chr12:34383128-34383129	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs563136264	chr12:34383130-34383131	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs192658017	chr12:34383147-34383148	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs569887383	chr12:34383192-34383193	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs184996783	chr12:34383211-34383212	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs59728650	chr12:34383214-34383215	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145610305	chr12:34383225-34383226	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs551773709	chr12:34383227-34383228	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs560485693	chr12:34383283-34383284	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs114703210	chr12:34383290-34383291	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs115617952	chr12:34383317-34383318	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs567393697	chr12:34383347-34383348	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs112603971	chr12:34383357-34383358	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs375947992	chr12:34383400-34383401	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs375530743	chr12:34383426-34383427	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs549445863	chr12:34383485-34383486	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs376706771	chr12:34383523-34383524	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs55885152	chr12:34383552-34383553	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19214233	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34382600-34385600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:34388800-34389400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr12:34388800-34389800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr12:34389000-34389200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:34389000-34389200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
6	chr12:34389000-34389400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:34389000-34389400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:34389000-34389400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
9	chr12:34389000-34389400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr12:34389000-34389400	ZNF genes & repeats	Liver	Liver
11	chr12:34389000-34389400	ZNF genes & repeats	Brain Angular Gyrus	brain
12	chr12:34389000-34389400	ZNF genes & repeats	Fetal Brain Male	brain
13	chr12:34389000-34389400	ZNF genes & repeats	Fetal Heart	heart
14	chr12:34389000-34389400	ZNF genes & repeats	Fetal Kidney	kidney
15	chr12:34389000-34389400	ZNF genes & repeats	Fetal Lung	lung
16	chr12:34389000-34389400	Enhancers	Gastric	stomach
17	chr12:34389000-34389400	ZNF genes & repeats	Pancreas	Pancrea
18	chr12:34389000-34389400	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
19	chr12:34389000-34389600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
20	chr12:34389200-34389400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr12:34389400-34392000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr12:34392800-34394600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:34398400-34399800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:34399000-34399400	ZNF genes & repeats	Primary T cells from cord blood	blood
25	chr12:34412600-34412800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
26	chr12:34412800-34413200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr12:34413600-34414000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:34415600-34415800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
29	chr12:34415800-34431400	Weak transcription	Right Atrium	heart
30	chr12:34416600-34416800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr12:34416600-34417600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:34416800-34417200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:34417000-34417200	Bivalent/Poised TSS	Liver	Liver
34	chr12:34417000-34418600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr12:34418000-34418600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr12:34418200-34427200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr12:34418600-34427000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr12:34419200-34431400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
39	chr12:34426000-34426200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr12:34426000-34426200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr12:34426200-34427000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr12:34426200-34427200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr12:34426800-34431400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:34427000-34427200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
45	chr12:34427000-34427200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:34427000-34427200	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr12:34427000-34427200	Bivalent/Poised TSS	Gastric	stomach
48	chr12:34427000-34427400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
49	chr12:34427000-34427400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr12:34427000-34427400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell

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