Variant report

Variant	esv1793582
Chromosome Location	chr12:120426820-120427915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:489)
CpG islands
(count:245)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:120426946-120426970	K562	blood:	n/a	n/a
2	BACH1	chr12:120427640-120427818	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr12:120426133-120427103	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr12:120426645-120426999	GM12878	blood:	n/a	chr12:120426812-120426825 chr12:120426755-120426768 chr12:120426814-120426827
5	BHLHE40	chr12:120426388-120427256	K562	blood:	n/a	chr12:120426819-120426835 chr12:120426595-120426611 chr12:120426812-120426828 chr12:120426992-120427008 chr12:120426807-120426823
6	BHLHE40	chr12:120427649-120427835	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:120426527-120427257	GM12878	blood:	n/a	chr12:120426819-120426835 chr12:120426595-120426611 chr12:120426812-120426828 chr12:120426992-120427008 chr12:120426807-120426823
8	BRCA1	chr12:120426757-120426942	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr12:120427610-120427871	K562	blood:	n/a	n/a
10	CCNT2	chr12:120426485-120427334	K562	blood:	n/a	chr12:120426959-120426968 chr12:120426571-120426580
11	CCNT2	chr12:120427574-120427848	K562	blood:	n/a	n/a
12	CEBPB	chr12:120426848-120426936	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:120426321-120426993	Hela-S3	cervix:	n/a	n/a
14	CHD1	chr12:120427197-120427204	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr12:120427563-120428019	IMR90	lung:	n/a	n/a
16	CHD1	chr12:120427699-120427889	GM12878	blood:	n/a	n/a
17	CHD1	chr12:120427711-120427882	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr12:120426371-120427841	Hela-S3	cervix:	n/a	chr12:120426960-120426970 chr12:120426965-120426975 chr12:120426992-120427002 chr12:120427435-120427445
19	CHD2	chr12:120427635-120427848	GM12878	blood:	n/a	n/a
20	CHD2	chr12:120427300-120427421	HepG2	liver:	n/a	n/a
21	CHD2	chr12:120426789-120426904	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr12:120426373-120427938	HepG2	liver:	n/a	n/a
23	CREB1	chr12:120426488-120427436	A549	lung:	n/a	n/a
24	CREB1	chr12:120427577-120427805	A549	lung:	n/a	n/a
25	CTCF	chr12:120427194-120427317	GM19239	blood:	n/a	n/a
26	CTCF	chr12:120426263-120427017	K562	blood:	n/a	n/a
27	CTCF	chr12:120427679-120427737	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr12:120427140-120427290	GM12874	blood:	n/a	n/a
29	CTCF	chr12:120426840-120426990	SAEC	small airway:	n/a	n/a
30	CTCF	chr12:120427254-120427282	GM12892	blood:	n/a	n/a
31	CTCF	chr12:120427102-120427335	K562	blood:	n/a	n/a
32	CTCF	chr12:120426820-120426970	GM12871	blood:	n/a	n/a
33	CTCF	chr12:120426780-120426930	K562	blood:	n/a	n/a
34	CTCF	chr12:120427140-120427290	GM12866	blood:	n/a	n/a
35	CTCF	chr12:120426925-120426929	GM10248	blood:	n/a	n/a
36	CTCF	chr12:120426940-120427090	GM12872	blood:	n/a	chr12:120427019-120427032
37	CTCF	chr12:120426780-120426930	GM12868	blood:	n/a	n/a
38	CTCF	chr12:120427160-120427310	GM12875	blood:	n/a	n/a
39	CTCF	chr12:120426794-120426915	GM19240	blood:	n/a	n/a
40	CTCF	chr12:120427163-120427403	Fibrobl	skin:	n/a	n/a
41	CTCF	chr12:120427180-120427330	GM12874	blood:	n/a	n/a
42	CTCF	chr12:120426740-120426890	AG04449	skin:	n/a	n/a
43	CTCF	chr12:120427140-120427290	HMEC	breast:	n/a	n/a
44	CTCF	chr12:120426840-120426990	GM12870	blood:	n/a	n/a
45	CTCF	chr12:120427160-120427310	GM12868	blood:	n/a	n/a
46	CTCF	chr12:120426807-120426904	NHEK	skin:	n/a	n/a
47	CTCF	chr12:120427155-120427333	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:120426789-120426960	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:120426720-120426870	HepG2	liver:	n/a	n/a
50	CTCF	chr12:120427207-120427311	H1-hESC	embryonic stem cell:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120426784-120426834	K562	blood:	n/a
2	chr12:120426784-120426834	K562	blood:	n/a
3	chr12:120426784-120426834	HAEpiC	amniotic membrane:	n/a
4	chr12:120427667-120427717	PANC-1	pancreas:	n/a
5	chr12:120426784-120426834	RPTEC	kidney:	n/a
6	chr12:120426784-120426834	ProgFib	skin:	n/a
7	chr12:120427178-120427228	Caco-2	colon:	n/a
8	chr12:120427182-120427232	SAEC	small airway:	n/a
9	chr12:120427182-120427232	HAEpiC	amniotic membrane:	n/a
10	chr12:120427667-120427717	U87	brain:	n/a
11	chr12:120427667-120427717	HRE	kidney:	n/a
12	chr12:120427178-120427228	ovcar-3	ovarian:	n/a
13	chr12:120427178-120427228	SK-N-SH_RA	brain:	n/a
14	chr12:120427178-120427228	HCM	heart:	n/a
15	chr12:120427178-120427228	NHBE	bronchial:	n/a
16	chr12:120427182-120427232	Hela-S3	cervix:	n/a
17	chr12:120427182-120427232	HIPEpiC	eye:	n/a
18	chr12:120426784-120426834	GM12892	blood:	n/a
19	chr12:120427667-120427717	Hepatocyte	liver:	n/a
20	chr12:120427667-120427717	AG04450	lung:	fetal
21	chr12:120427182-120427232	AG04449	skin:	fetal
22	chr12:120427182-120427232	PFSK-1	brain:	n/a
23	chr12:120427667-120427717	SK-N-SH_RA	brain:	n/a
24	chr12:120426784-120426834	HCM	heart:	n/a
25	chr12:120427178-120427228	Jurkat	blood:	n/a
26	chr12:120427667-120427717	LNCaP	prostate:	n/a
27	chr12:120427178-120427228	MCF10A-Er-Src	breast:	n/a
28	chr12:120427182-120427232	AG10803	skin:	n/a
29	chr12:120427667-120427717	HEEpiC	esophagus:	n/a
30	chr12:120427178-120427228	ECC-1	luminal epithelium:	n/a
31	chr12:120426784-120426834	HRE	kidney:	n/a
32	chr12:120427182-120427232	A549	lung:	n/a
33	chr12:120427182-120427232	AoSMC	blood vessel:	n/a
34	chr12:120427182-120427232	NB4	blood:	n/a
35	chr12:120427667-120427717	SAEC	small airway:	n/a
36	chr12:120427667-120427717	A549	lung:	n/a
37	chr12:120427182-120427232	MCF10A-Er-Src	breast:	n/a
38	chr12:120427667-120427717	NH-A	brain:	n/a
39	chr12:120426784-120426834	AG10803	skin:	n/a
40	chr12:120426784-120426834	Jurkat	blood:	n/a
41	chr12:120427667-120427717	GM12891	blood:	n/a
42	chr12:120427178-120427228	NHDF-neo	bronchial:	n/a
43	chr12:120426784-120426834	HCF	heart:	n/a
44	chr12:120426784-120426834	AG04450	lung:	fetal
45	chr12:120427178-120427228	RPTEC	kidney:	n/a
46	chr12:120427182-120427232	HCT-116	colon:	n/a
47	chr12:120427667-120427717	HepG2	liver:	n/a
48	chr12:120427667-120427717	NT2-D1	testis:	n/a
49	chr12:120427178-120427228	SK-N-SH	brain:	n/a
50	chr12:120426784-120426834	HCPEpiC	choroid plexus:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120425977..120426934-chr12:120517209..120518213,3	MCF-7	breast:
2	chr12:120420153..120423656-chr12:120424541..120427660,4	MCF-7	breast:
3	chr12:120425209..120429306-chr12:120552934..120555400,5	MCF-7	breast:
4	chr12:120425735..120427312-chr12:120553344..120556119,2	MCF-7	breast:
5	chr12:120425404..120428200-chr12:120435927..120438924,2	K562	blood:
6	chr12:120425546..120427435-chr12:120477512..120479258,2	MCF-7	breast:
7	chr12:120420772..120424084-chr12:120424860..120426963,3	MCF-7	breast:
8	chr12:120426493..120428297-chr12:120534910..120538709,3	MCF-7	breast:
9	chr12:120426261..120428229-chr12:120638078..120640091,2	MCF-7	breast:
10	chr12:120426002..120427624-chr12:120517341..120518989,2	MCF-7	breast:
11	chr12:120427745..120429727-chr12:120729725..120731576,2	MCF-7	breast:
12	chr12:120427086..120431307-chr12:120435070..120439124,5	MCF-7	breast:
13	chr12:120426746..120427474-chr12:133338037..133338792,2	HCT-116	colon:
14	chr12:120424699..120427677-chr12:120728453..120732318,6	K562	blood:
15	chr12:120424138..120428272-chr12:120728453..120731316,5	K562	blood:
16	chr12:120426492..120427432-chr12:120524501..120525382,2	K562	blood:
17	chr12:120313729..120318058-chr12:120425281..120428238,3	K562	blood:
18	chr12:120426620..120429059-chr12:120727400..120730169,3	MCF-7	breast:
19	chr12:120426982..120427577-chr19:56825701..56826223,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
CCDC64	TF binding region
CCDC64	CpG island
ENSG00000200795	chromatin interactions
ENSG00000131848	chromatin interactions
ENSG00000111737	chromatin interactions
ENSG00000267549	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000176915	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000135127	chromatin interactions
ENSG00000255857	chromatin interactions
ENSG00000122966	chromatin interactions

Extended variants
information (count: 25 )
Associated
traits (count: 71 )

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	rs79878785	chr12:120426826-120426827	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs564449072	chr12:120426878-120426879	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs578167054	chr12:120426898-120426899	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs117426293	chr12:120426905-120426906	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs560134979	chr12:120426946-120426947	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs529036769	chr12:120426952-120426953	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs549016583	chr12:120426955-120426956	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs562767456	chr12:120427008-120427009	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs531480554	chr12:120427040-120427041	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs7306494	chr12:120427075-120427076	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs10603226	chr12:120427097-120427098	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs201855386	chr12:120427266-120427267	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs71745796	chr12:120427267-120427268	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs112694456	chr12:120427284-120427285	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs140135341	chr12:120427384-120427385	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs547424498	chr12:120427394-120427395	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs566963586	chr12:120427495-120427496	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs111440037	chr12:120427574-120427575	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs536015945	chr12:120427587-120427588	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs555811021	chr12:120427720-120427721	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs575918655	chr12:120427737-120427738	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs538521402	chr12:120427750-120427751	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs558221602	chr12:120427752-120427753	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs11614571	chr12:120427787-120427788	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs578066392	chr12:120427816-120427817	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120426000-120427400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:120426200-120427000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:120426200-120427400	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr12:120426200-120427400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
5	chr12:120426200-120427800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr12:120426200-120427800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
7	chr12:120426200-120428000	Active TSS	H1 Cell Line	embryonic stem cell
8	chr12:120426200-120428000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:120426200-120428000	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr12:120426200-120428000	Active TSS	Sigmoid Colon	Sigmoid Colon
11	chr12:120426200-120428200	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr12:120426200-120428200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr12:120426200-120428200	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr12:120426200-120428400	Active TSS	Rectal Smooth Muscle	rectum
15	chr12:120426200-120428600	Active TSS	H9 Cell Line	embryonic stem cell
16	chr12:120426200-120429400	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr12:120426400-120427000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:120426400-120427000	Flanking Active TSS	Right Ventricle	heart
19	chr12:120426400-120427000	Flanking Active TSS	Dnd41	blood
20	chr12:120426400-120427200	Flanking Active TSS	Stomach Smooth Muscle	stomach
21	chr12:120426400-120427400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:120426400-120427400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr12:120426400-120427400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:120426400-120427400	Flanking Active TSS	Liver	Liver
25	chr12:120426400-120427800	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr12:120426400-120427800	Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr12:120426400-120427800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:120426400-120427800	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr12:120426400-120427800	Active TSS	Primary T cells from cord blood	blood
30	chr12:120426400-120427800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:120426400-120427800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr12:120426400-120427800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr12:120426400-120427800	Active TSS	Brain Cingulate Gyrus	brain
34	chr12:120426400-120427800	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr12:120426400-120427800	Active TSS	A549	lung
36	chr12:120426400-120427800	Active TSS	NHEK	skin
37	chr12:120426400-120427800	Active TSS	Osteobl	bone
38	chr12:120426400-120428000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:120426400-120428000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr12:120426400-120428000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr12:120426400-120428000	Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr12:120426400-120428000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr12:120426400-120428000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:120426400-120428000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:120426400-120428000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr12:120426400-120428000	Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr12:120426400-120428000	Active TSS	Brain Germinal Matrix	brain
48	chr12:120426400-120428000	Active TSS	Fetal Intestine Small	intestine
49	chr12:120426400-120428000	Active TSS	Hela-S3	cervix
50	chr12:120426400-120428000	Active TSS	HSMMtube	muscle

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