Variant report

Variant	nsv1039604
Chromosome Location	chr12:34312577-34435009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1253)
CpG islands
(count:1648)
Chromatin interactive
region (count:27)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	ARID3A	chr12:34367118-34367148	K562	blood:	n/a	n/a
3	ARID3A	chr12:34372445-34372838	K562	blood:	n/a	n/a
4	ATF1	chr12:34372443-34372838	K562	blood:	n/a	n/a
5	ATF1	chr12:34340026-34340130	K562	blood:	n/a	n/a
6	ATF1	chr12:34430831-34430993	K562	blood:	n/a	n/a
7	ATF1	chr12:34407159-34407233	K562	blood:	n/a	n/a
8	ATF3	chr12:34372504-34372902	A549	lung:	n/a	n/a
9	ATF3	chr12:34372398-34372788	A549	lung:	n/a	n/a
10	BACH1	chr12:34429857-34430227	K562	blood:	n/a	n/a
11	BACH1	chr12:34369832-34370042	K562	blood:	n/a	n/a
12	BACH1	chr12:34417965-34418172	K562	blood:	n/a	n/a
13	BACH1	chr12:34417075-34417361	K562	blood:	n/a	n/a
14	BACH1	chr12:34429537-34429559	K562	blood:	n/a	n/a
15	BACH1	chr12:34428886-34428914	K562	blood:	n/a	n/a
16	BATF	chr12:34387277-34387522	GM12878	blood:	n/a	n/a
17	BATF	chr12:34374801-34375081	GM12878	blood:	n/a	n/a
18	BATF	chr12:34372475-34372720	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:34367954-34368142	GM12878	blood:	n/a	n/a
20	BCL3	chr12:34372532-34372732	GM12878	blood:	n/a	n/a
21	BCL3	chr12:34372500-34372832	A549	lung:	n/a	n/a
22	BCLAF1	chr12:34372504-34372752	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:34372453-34372844	K562	blood:	n/a	n/a
24	BHLHE40	chr12:34357708-34357899	K562	blood:	n/a	n/a
25	BHLHE40	chr12:34371217-34371696	K562	blood:	n/a	n/a
26	BHLHE40	chr12:34417073-34417446	K562	blood:	n/a	n/a
27	BHLHE40	chr12:34428714-34428914	K562	blood:	n/a	n/a
28	BHLHE40	chr12:34328719-34328742	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:34417796-34417999	K562	blood:	n/a	n/a
30	BHLHE40	chr12:34429855-34430232	K562	blood:	n/a	n/a
31	BRCA1	chr12:34371358-34371611	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr12:34372453-34372842	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr12:34429859-34430235	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr12:34362157-34362478	GM12878	blood:	n/a	n/a
35	BRCA1	chr12:34429446-34429561	GM12878	blood:	n/a	n/a
36	BRCA1	chr12:34372453-34372841	HepG2	liver:	n/a	n/a
37	BRCA1	chr12:34429536-34429561	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr12:34429856-34430234	GM12878	blood:	n/a	n/a
39	BRCA1	chr12:34367120-34367268	GM12878	blood:	n/a	n/a
40	BRCA1	chr12:34417797-34418168	GM12878	blood:	n/a	n/a
41	BRCA1	chr12:34417803-34417997	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr12:34417092-34417445	GM12878	blood:	n/a	n/a
43	CEBPB	chr12:34432648-34432896	HepG2	liver:	n/a	chr12:34432753-34432764
44	CEBPB	chr12:34341977-34342278	A549	lung:	n/a	chr12:34342091-34342100 chr12:34342091-34342102 chr12:34342119-34342132 chr12:34342120-34342131 chr12:34342089-34342102 chr12:34342089-34342100 chr12:34342119-34342130
45	CEBPB	chr12:34370851-34371004	K562	blood:	n/a	n/a
46	CEBPB	chr12:34406746-34407058	K562	blood:	n/a	n/a
47	CEBPB	chr12:34341921-34342286	K562	blood:	n/a	chr12:34342091-34342100 chr12:34342091-34342102 chr12:34342119-34342132 chr12:34342120-34342131 chr12:34342089-34342102 chr12:34342089-34342100 chr12:34342119-34342130
48	CEBPB	chr12:34415583-34415933	MCF-7	breast:	n/a	n/a
49	CEBPB	chr12:34362439-34362466	HepG2	liver:	n/a	n/a
50	CEBPB	chr12:34361630-34361854	HepG2	liver:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34362315-34362365	RPTEC	kidney:	n/a
2	chr12:34362315-34362365	RPTEC	kidney:	n/a
3	chr12:34371861-34371911	RPTEC	kidney:	n/a
4	chr12:34371529-34371579	PrEC	prostate:	n/a
5	chr12:34319939-34319989	HEEpiC	esophagus:	n/a
6	chr12:34317569-34317619	SAEC	small airway:	n/a
7	chr12:34362529-34362579	SAEC	small airway:	n/a
8	chr12:34358399-34358449	NHBE	bronchial:	n/a
9	chr12:34317983-34318033	Caco-2	colon:	n/a
10	chr12:34319822-34319872	LNCaP	prostate:	n/a
11	chr12:34361589-34361639	HCM	heart:	n/a
12	chr12:34319740-34319790	NT2-D1	testis:	n/a
13	chr12:34371784-34371834	GM12892	blood:	n/a
14	chr12:34319734-34319784	GM12891	blood:	n/a
15	chr12:34318704-34318754	AG09319	gingival:	n/a
16	chr12:34323943-34323993	NHDF-neo	bronchial:	n/a
17	chr12:34319740-34319790	PFSK-1	brain:	n/a
18	chr12:34371529-34371579	HRCEpiC	kidney:	n/a
19	chr12:34319740-34319790	NH-A	brain:	n/a
20	chr12:34319740-34319790	LNCaP	prostate:	n/a
21	chr12:34319740-34319790	Hepatocyte	liver:	n/a
22	chr12:34363587-34363637	PrEC	prostate:	n/a
23	chr12:34371529-34371579	GM06990	blood:	n/a
24	chr12:34318115-34318165	HCM	heart:	n/a
25	chr12:34317569-34317619	HMEC	breast:	n/a
26	chr12:34318704-34318754	HCF	heart:	n/a
27	chr12:34358399-34358449	GM12892	blood:	n/a
28	chr12:34372299-34372349	IMR90	lung:	fetal
29	chr12:34361006-34361056	HIPEpiC	eye:	n/a
30	chr12:34318115-34318165	Hepatocyte	liver:	n/a
31	chr12:34371861-34371911	SK-N-SH	brain:	n/a
32	chr12:34363872-34363922	GM19239	blood:	n/a
33	chr12:34371784-34371834	HEEpiC	esophagus:	n/a
34	chr12:34361006-34361056	ovcar-3	ovarian:	n/a
35	chr12:34362315-34362365	ProgFib	skin:	n/a
36	chr12:34374453-34374503	GM12891	blood:	n/a
37	chr12:34318115-34318165	HEK293	kidney:	embryo
38	chr12:34361006-34361056	Jurkat	blood:	n/a
39	chr12:34319734-34319784	PrEC	prostate:	n/a
40	chr12:34361589-34361639	Hepatocyte	liver:	n/a
41	chr12:34319734-34319784	NHDF-neo	bronchial:	n/a
42	chr12:34323943-34323993	NH-A	brain:	n/a
43	chr12:34371861-34371911	AG10803	skin:	n/a
44	chr12:34371529-34371579	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:34323943-34323993	HUVEC	blood vessel:	n/a
46	chr12:34319822-34319872	AG04449	skin:	fetal
47	chr12:34367670-34367720	ovcar-3	ovarian:	n/a
48	chr12:34374453-34374503	HMEC	breast:	n/a
49	chr12:34318527-34318577	HCF	heart:	n/a
50	chr12:34361589-34361639	AoSMC	blood vessel:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:34405769..34407368-chr12:38464924..38466718,2	K562	blood:
2	chr12:34372136..34372665-chr12:127650606..127651138,2	MCF-7	breast:
3	chr1:91852303..91852973-chr12:34372638..34373146,2	HCT-116	colon:
4	chr12:34372145..34372649-chr9:79186173..79186679,2	MCF-7	breast:
5	chr12:34416748..34417268-chr2:133025884..133026405,2	MCF-7	breast:
6	chr12:34376481..34379453-chr12:34384361..34386376,2	K562	blood:
7	chr12:34372661..34373161-chrX:108297704..108298236,2	HCT-116	colon:
8	chr1:91852330..91853034-chr12:34372628..34373167,11	MCF-7	breast:
9	chr12:34371140..34372648-chr12:127650511..127652141,3	MCF-7	breast:
10	chr12:34416477..34418281-chr16:33956682..33958772,3	MCF-7	breast:
11	chr12:34277684..34281105-chr12:34367413..34370316,3	K562	blood:
12	chr12:34275785..34276629-chr12:34339119..34339912,4	MCF-7	breast:
13	chr12:34367163..34367683-chr14:88237196..88237802,3	MCF-7	breast:
14	chr12:34372126..34372636-chr12:127650618..127651388,2	MCF-7	breast:
15	chr12:34372131..34372654-chr9:79186162..79186868,3	MCF-7	breast:
16	chr12:34277684..34280343-chr12:34367543..34370316,2	K562	blood:
17	chr12:34376481..34379453-chr12:34384361..34386376,2	K562	blood:
18	chr12:34371158..34372658-chr9:79185159..79186851,2	K562	blood:
19	chr1:91852355..91852916-chr12:34372634..34373168,4	MCF-7	breast:
20	chr1:91852357..91853118-chr12:34372627..34373168,5	MCF-7	breast:
21	chr12:34372126..34372647-chr12:127650887..127651388,2	MCF-7	breast:
22	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
23	chr1:91851338..91852967-chr12:34372628..34374131,2	K562	blood:
24	chr1:91852282..91853087-chr12:34372625..34373157,6	MCF-7	breast:
25	chr12:34427757..34428277-chr16:33958747..33959470,2	MCF-7	breast:
26	chr1:91851344..91853074-chr12:34372634..34374167,5	MCF-7	breast:
27	chr1:91851334..91853102-chr12:34372625..34374158,7	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-5	chr12:34430929-34431017	NONHSAT027661
2	lnc-ALG10-4	chr12:34402416-34402893	NONHSAT140067
3	lnc-ALG10-3	chr12:34315397-34315903	NONHSAT027653
4	lnc-ALG10-5	chr12:34421984-34422141	NONHSAT027661
5	lnc-ALG10-2	chr12:34315112-34315173	ENSG00000255628

No data

Variant related genes	Relation type
ENSG00000255652	TF binding region
ENSG00000256986	TF binding region
ENSG00000272435	TF binding region
ENSG00000258794	TF binding region
TUBB8P4	TF binding region
ENSG00000256614	TF binding region
ENSG00000255652	CpG island
ENSG00000256986	CpG island
ENSG00000272435	CpG island
ENSG00000258794	CpG island
TUBB8P4	CpG island
ENSG00000256614	CpG island
ENSG00000241781	chromatin interactions
ENSG00000226958	chromatin interactions
ENSG00000239776	chromatin interactions

Extended variants
information (count: 3539 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3539 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75178095	chr12:34313834-34313835	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs55679728	chr12:34313841-34313842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs546526698	chr12:34313848-34313849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs75803311	chr12:34313874-34313875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs78109593	chr12:34313884-34313885	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs116141512	chr12:34313899-34313900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs199803103	chr12:34313903-34313904	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201171083	chr12:34313929-34313930	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534258591	chr12:34313975-34313976	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs112959599	chr12:34313977-34313978	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs180765365	chr12:34313996-34313997	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs554059458	chr12:34314034-34314035	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573967526	chr12:34314044-34314045	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs145611649	chr12:34314067-34314068	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs74073504	chr12:34314115-34314116	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs576499046	chr12:34314116-34314117	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs185216876	chr12:34314118-34314119	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs188514944	chr12:34314129-34314130	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs527670337	chr12:34314140-34314141	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547776091	chr12:34314162-34314163	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs560470357	chr12:34314207-34314208	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs148836111	chr12:34314281-34314282	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs548912686	chr12:34314293-34314294	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs569031822	chr12:34314307-34314308	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs567969938	chr12:34314315-34314316	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs181599834	chr12:34314331-34314332	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs528930148	chr12:34314332-34314333	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs550241837	chr12:34314352-34314353	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs11613903	chr12:34314362-34314363	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs79922818	chr12:34314366-34314367	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs78826540	chr12:34314371-34314372	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs113687782	chr12:34314417-34314418	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs373325645	chr12:34314426-34314427	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs58974949	chr12:34314428-34314429	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs75894858	chr12:34314469-34314470	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs568648732	chr12:34314508-34314509	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533565491	chr12:34314533-34314534	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs553305388	chr12:34314540-34314541	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569893751	chr12:34314563-34314564	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567629677	chr12:34314567-34314568	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs537587626	chr12:34314570-34314571	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs536537626	chr12:34314572-34314573	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556525144	chr12:34314637-34314638	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs576556739	chr12:34314653-34314654	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs186564306	chr12:34314682-34314683	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs559022745	chr12:34314723-34314724	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs111831962	chr12:34314748-34314749	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs116194066	chr12:34314771-34314772	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs57391398	chr12:34314776-34314777	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12829125	chr12:34314789-34314790	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:55)

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
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	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

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34314000-34320600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:34319200-34320200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:34319800-34320000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:34328600-34328800	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
5	chr12:34336800-34345400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr12:34338000-34340200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr12:34339200-34340000	Enhancers	Primary B cells from peripheral blood	blood
8	chr12:34340000-34341600	Weak transcription	Primary B cells from peripheral blood	blood
9	chr12:34341200-34341600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:34341400-34341800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr12:34341600-34342200	Enhancers	Primary B cells from peripheral blood	blood
12	chr12:34342200-34342600	Weak transcription	Primary B cells from peripheral blood	blood
13	chr12:34342400-34343000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr12:34342400-34343400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:34342600-34343800	Enhancers	Primary hematopoietic stem cells	blood
16	chr12:34342600-34343800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:34342600-34344400	Enhancers	Primary B cells from peripheral blood	blood
18	chr12:34343000-34343600	Enhancers	Primary B cells from cord blood	blood
19	chr12:34343400-34343600	Enhancers	Spleen	Spleen
20	chr12:34356800-34359400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:34357000-34358400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr12:34357000-34359200	Enhancers	Primary B cells from peripheral blood	blood
23	chr12:34357200-34357600	Enhancers	Primary B cells from cord blood	blood
24	chr12:34357600-34357800	Enhancers	Spleen	Spleen
25	chr12:34358400-34358600	Enhancers	Spleen	Spleen
26	chr12:34358800-34359000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr12:34360000-34362800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr12:34360400-34363600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr12:34360800-34363200	ZNF genes & repeats	Fetal Stomach	stomach
30	chr12:34361400-34363600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr12:34361400-34364000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:34361400-34365000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:34361600-34362400	ZNF genes & repeats	HepG2	liver
34	chr12:34361600-34362600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
35	chr12:34361600-34362600	ZNF genes & repeats	Gastric	stomach
36	chr12:34361600-34362600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
37	chr12:34361600-34363800	ZNF genes & repeats	Pancreas	Pancrea
38	chr12:34361800-34362200	ZNF genes & repeats	Adipose Nuclei	Adipose
39	chr12:34361800-34362600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr12:34361800-34362600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:34361800-34362600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
42	chr12:34361800-34362600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
43	chr12:34361800-34362600	ZNF genes & repeats	Colonic Mucosa	Colon
44	chr12:34361800-34362600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
45	chr12:34361800-34362600	ZNF genes & repeats	Lung	lung
46	chr12:34361800-34362600	ZNF genes & repeats	Spleen	Spleen
47	chr12:34361800-34362600	ZNF genes & repeats	NHEK	skin
48	chr12:34362000-34362400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
49	chr12:34362000-34362600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
50	chr12:34362000-34362600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle

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