Variant report

Variant	nsv428277
Chromosome Location	chr12:34394298-34571308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1248)
CpG islands
(count:8668)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1248 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr12:34486593-34486711	K562	blood:	n/a	n/a
7	BACH1	chr12:34428886-34428914	K562	blood:	n/a	n/a
8	BACH1	chr12:34429537-34429559	K562	blood:	n/a	n/a
9	BACH1	chr12:34489607-34489683	K562	blood:	n/a	n/a
10	BACH1	chr12:34417965-34418172	K562	blood:	n/a	n/a
11	BACH1	chr12:34417075-34417361	K562	blood:	n/a	n/a
12	BACH1	chr12:34500299-34500489	K562	blood:	n/a	n/a
13	BACH1	chr12:34429857-34430227	K562	blood:	n/a	n/a
14	BHLHE40	chr12:34501108-34501225	K562	blood:	n/a	n/a
15	BHLHE40	chr12:34500243-34500651	K562	blood:	n/a	chr12:34500434-34500450
16	BHLHE40	chr12:34489695-34490283	K562	blood:	n/a	chr12:34490108-34490124
17	BHLHE40	chr12:34544817-34545121	K562	blood:	n/a	n/a
18	BHLHE40	chr12:34488959-34488987	K562	blood:	n/a	n/a
19	BHLHE40	chr12:34499722-34499980	K562	blood:	n/a	n/a
20	BHLHE40	chr12:34499008-34499021	K562	blood:	n/a	n/a
21	BHLHE40	chr12:34417073-34417446	K562	blood:	n/a	n/a
22	BHLHE40	chr12:34417796-34417999	K562	blood:	n/a	n/a
23	BHLHE40	chr12:34509153-34509543	K562	blood:	n/a	n/a
24	BHLHE40	chr12:34503265-34503867	K562	blood:	n/a	chr12:34503364-34503380
25	BHLHE40	chr12:34484701-34484766	K562	blood:	n/a	n/a
26	BHLHE40	chr12:34428714-34428914	K562	blood:	n/a	n/a
27	BHLHE40	chr12:34494224-34494316	K562	blood:	n/a	n/a
28	BHLHE40	chr12:34429855-34430232	K562	blood:	n/a	n/a
29	BHLHE40	chr12:34501989-34502240	K562	blood:	n/a	n/a
30	BRCA1	chr12:34417092-34417445	GM12878	blood:	n/a	n/a
31	BRCA1	chr12:34429859-34430235	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr12:34516242-34516252	HepG2	liver:	n/a	n/a
33	BRCA1	chr12:34429446-34429561	GM12878	blood:	n/a	n/a
34	BRCA1	chr12:34417803-34417997	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr12:34429536-34429561	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr12:34429856-34430234	GM12878	blood:	n/a	n/a
37	BRCA1	chr12:34417797-34418168	GM12878	blood:	n/a	n/a
38	CBX3	chr12:34438330-34438744	K562	blood:	n/a	n/a
39	CBX3	chr12:34488602-34489199	K562	blood:	n/a	n/a
40	CBX3	chr12:34438299-34438731	K562	blood:	n/a	n/a
41	CBX3	chr12:34500168-34500641	K562	blood:	n/a	n/a
42	CBX3	chr12:34486285-34486611	K562	blood:	n/a	n/a
43	CBX3	chr12:34503332-34503995	K562	blood:	n/a	n/a
44	CBX3	chr12:34489373-34490412	K562	blood:	n/a	n/a
45	CBX3	chr12:34560747-34561019	K562	blood:	n/a	n/a
46	CBX3	chr12:34438038-34438225	K562	blood:	n/a	n/a
47	CBX3	chr12:34499643-34499985	K562	blood:	n/a	n/a
48	CCNT2	chr12:34503324-34503866	K562	blood:	n/a	n/a
49	CCNT2	chr12:34488797-34489551	K562	blood:	n/a	n/a
50	CCNT2	chr12:34489857-34490127	K562	blood:	n/a	n/a

(count:8668 , 50 per page) page: 1 2 3 4 5 6 7 ... 174

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34532907-34532957	BE2_C	brain:	n/a
2	chr12:34448653-34448703	ovcar-3	ovarian:	n/a
3	chr12:34477398-34477448	HepG2	liver:	n/a
4	chr12:34506462-34506512	AG10803	skin:	n/a
5	chr12:34478388-34478438	NHBE	bronchial:	n/a
6	chr12:34494852-34494902	MCF-7	breast:	n/a
7	chr12:34532907-34532957	BE2_C	brain:	n/a
8	chr12:34448653-34448703	ovcar-3	ovarian:	n/a
9	chr12:34477398-34477448	HepG2	liver:	n/a
10	chr12:34506462-34506512	AG10803	skin:	n/a
11	chr12:34478388-34478438	NHBE	bronchial:	n/a
12	chr12:34494852-34494902	MCF-7	breast:	n/a
13	chr12:34552411-34552461	MCF-7	breast:	n/a
14	chr12:34471260-34471310	HL-60	blood:	n/a
15	chr12:34534365-34534415	BJ	skin:	n/a
16	chr12:34503503-34503553	HAEpiC	amniotic membrane:	n/a
17	chr12:34457072-34457122	PANC-1	pancreas:	n/a
18	chr12:34506462-34506512	HMEC	breast:	n/a
19	chr12:34507257-34507307	MCF10A-Er-Src	breast:	n/a
20	chr12:34493996-34494046	SKMC	muscle:	n/a
21	chr12:34452063-34452113	AG09309	skin:	n/a
22	chr12:34471143-34471193	HCF	heart:	n/a
23	chr12:34501300-34501350	SK-N-SH_RA	brain:	n/a
24	chr12:34445021-34445071	MCF10A-Er-Src	breast:	n/a
25	chr12:34485526-34485576	PFSK-1	brain:	n/a
26	chr12:34536156-34536206	NHDF-neo	bronchial:	n/a
27	chr12:34492938-34492988	AG04449	skin:	fetal
28	chr12:34443436-34443486	HNPCEpiC	eye:	n/a
29	chr12:34447816-34447866	IMR90	lung:	fetal
30	chr12:34442705-34442755	HCM	heart:	n/a
31	chr12:34478388-34478438	Hela-S3	cervix:	n/a
32	chr12:34498372-34498422	HEEpiC	esophagus:	n/a
33	chr12:34452063-34452113	NT2-D1	testis:	n/a
34	chr12:34453300-34453350	HL-60	blood:	n/a
35	chr12:34527230-34527280	HCM	heart:	n/a
36	chr12:34480142-34480192	HepG2	liver:	n/a
37	chr12:34547337-34547387	GM06990	blood:	n/a
38	chr12:34507257-34507307	T-47D	breast:	n/a
39	chr12:34480428-34480478	Caco-2	colon:	n/a
40	chr12:34446650-34446700	PrEC	prostate:	n/a
41	chr12:34528521-34528571	PFSK-1	brain:	n/a
42	chr12:34453498-34453548	ECC-1	luminal epithelium:	n/a
43	chr12:34511909-34511959	PANC-1	pancreas:	n/a
44	chr12:34532907-34532957	PFSK-1	brain:	n/a
45	chr12:34530799-34530849	AG04449	skin:	fetal
46	chr12:34529645-34529695	NH-A	brain:	n/a
47	chr12:34453300-34453350	PrEC	prostate:	n/a
48	chr12:34480142-34480192	T-47D	breast:	n/a
49	chr12:34489995-34490045	HNPCEpiC	eye:	n/a
50	chr12:34552411-34552461	SK-N-SH_RA	brain:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:34500138..34502153-chr12:34504147..34506890,2	K562	blood:
2	chr12:34501359..34504154-chr12:34510668..34513544,2	K562	blood:
3	chr12:34472451..34474607-chr12:34482688..34484610,2	K562	blood:
4	chr12:34472451..34474607-chr12:34482688..34484610,2	K562	blood:
5	chr12:34542219..34546005-chr12:34547286..34550175,4	K562	blood:
6	chr12:34497467..34501951-chr12:34506676..34509735,4	K562	blood:
7	chr12:34513093..34516192-chr12:34527570..34530403,3	K562	blood:
8	chr12:34497129..34499259-chr12:34508235..34509796,2	K562	blood:
9	chr12:34491491..34493706-chr12:34544208..34545803,2	K562	blood:
10	chr12:34487742..34489883-chr12:34492282..34495193,2	K562	blood:
11	chr12:34491491..34493706-chr12:34544208..34545803,2	K562	blood:
12	chr12:34416748..34417268-chr2:133025884..133026405,2	MCF-7	breast:
13	chr12:34497610..34503522-chr12:34523490..34528831,5	K562	blood:
14	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:
15	chr12:34405769..34407368-chr12:38464924..38466718,2	K562	blood:
16	chr12:34544160..34546005-chr12:34547460..34549884,2	K562	blood:
17	chr12:34497467..34501951-chr12:34506676..34509735,4	K562	blood:
18	chr12:34543477..34545374-chr12:34550348..34552407,2	K562	blood:
19	chr12:34487742..34489883-chr12:34492282..34495193,2	K562	blood:
20	chr12:34279057..34280887-chr12:34440053..34441876,2	K562	blood:
21	chr12:34500138..34502153-chr12:34504147..34506890,2	K562	blood:
22	chr12:34543477..34545374-chr12:34550348..34552407,2	K562	blood:
23	chr12:34416477..34418281-chr16:33956682..33958772,3	MCF-7	breast:
24	chr12:34497610..34503522-chr12:34523490..34528831,5	K562	blood:
25	chr12:34544160..34546005-chr12:34547460..34549884,2	K562	blood:
26	chr12:34542219..34546005-chr12:34547286..34550175,4	K562	blood:
27	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
28	chr12:34513093..34516192-chr12:34527570..34530403,3	K562	blood:
29	chr12:34497129..34499259-chr12:34508235..34509796,2	K562	blood:
30	chr12:34501359..34504154-chr12:34510668..34513544,2	K562	blood:
31	chr12:34427757..34428277-chr16:33958747..33959470,2	MCF-7	breast:
32	chr12:34480099..34482680-chr12:34485043..34486658,2	K562	blood:
33	chr12:34480099..34482680-chr12:34485043..34486658,2	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
ENSG00000256614	TF binding region
ENSG00000256614	CpG island

Extended variants
information (count: 10783 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:10783 , 50 per page) page: 1 2 3 4 5 6 7 ... 216

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80227712	chr12:34394321-34394322	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs188542063	chr12:34394377-34394378	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs576158152	chr12:34394412-34394413	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs193239203	chr12:34394422-34394423	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs145312125	chr12:34394455-34394456	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs376031459	chr12:34394456-34394457	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs73100250	chr12:34394486-34394487	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs115935950	chr12:34394536-34394537	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs560422209	chr12:34394556-34394557	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs73100252	chr12:34394560-34394561	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs200891464	chr12:34394568-34394569	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs11053169	chr12:34394592-34394593	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574224279	chr12:34397659-34397660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs138687739	chr12:34397730-34397731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs527300569	chr12:34397746-34397747	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563000975	chr12:34397772-34397773	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs11614133	chr12:34397786-34397787	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs369359230	chr12:34397825-34397826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs559808350	chr12:34397832-34397833	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs149386372	chr12:34397841-34397842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs541516854	chr12:34397848-34397849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs548526545	chr12:34397873-34397874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs568666919	chr12:34397906-34397907	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs563091472	chr12:34397930-34397931	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs537598618	chr12:34397955-34397956	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs114182777	chr12:34397966-34397967	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs184876224	chr12:34398008-34398009	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs145787296	chr12:34398053-34398054	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570912125	chr12:34398062-34398063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs530967031	chr12:34398087-34398088	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552365912	chr12:34398097-34398098	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs74899966	chr12:34398099-34398100	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs79289664	chr12:34398103-34398104	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs189922300	chr12:34398104-34398105	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs554392558	chr12:34398107-34398108	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs112344224	chr12:34398145-34398146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs116466994	chr12:34398153-34398154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs547004371	chr12:34398177-34398178	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs79156822	chr12:34398202-34398203	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs147478113	chr12:34398206-34398207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs573625925	chr12:34398228-34398229	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559278712	chr12:34398299-34398300	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs528829419	chr12:34398313-34398314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs548854673	chr12:34398329-34398330	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs192002412	chr12:34398356-34398357	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs138158078	chr12:34398357-34398358	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs74075611	chr12:34398384-34398385	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570975361	chr12:34398407-34398408	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184557887	chr12:34398430-34398431	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs143620516	chr12:34398451-34398452	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34392800-34394600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:34398400-34399800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:34399000-34399400	ZNF genes & repeats	Primary T cells from cord blood	blood
4	chr12:34412600-34412800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr12:34412800-34413200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr12:34413600-34414000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:34415600-34415800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr12:34415800-34431400	Weak transcription	Right Atrium	heart
9	chr12:34416600-34416800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr12:34416600-34417600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr12:34416800-34417200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:34417000-34417200	Bivalent/Poised TSS	Liver	Liver
13	chr12:34417000-34418600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:34418000-34418600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr12:34418200-34427200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr12:34418600-34427000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr12:34419200-34431400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr12:34426000-34426200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr12:34426000-34426200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr12:34426200-34427000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr12:34426200-34427200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr12:34426800-34431400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:34427000-34427200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr12:34427000-34427200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:34427000-34427200	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:34427000-34427200	Bivalent/Poised TSS	Gastric	stomach
27	chr12:34427000-34427400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
28	chr12:34427000-34427400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr12:34427000-34427400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
30	chr12:34427000-34427400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
31	chr12:34427000-34427400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr12:34427000-34427400	ZNF genes & repeats	Colon Smooth Muscle	Colon
33	chr12:34427000-34427600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr12:34427000-34428200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:34427200-34427400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
36	chr12:34427200-34427800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr12:34427200-34428600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr12:34429200-34431200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chr12:34429400-34431200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
40	chr12:34430400-34431400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
41	chr12:34430600-34431200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
42	chr12:34434200-34440800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
43	chr12:34438000-34439000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr12:34438800-34446600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:34439000-34441400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
46	chr12:34439200-34439800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
47	chr12:34439400-34445000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr12:34439400-34445400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr12:34440000-34446600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
50	chr12:34442200-34444000	Active TSS	K562	blood

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