Variant report

Variant	esv3427707
Chromosome Location	chr1:214780854-214783702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:428)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr1:214778944-214781267	K562	blood:	n/a	n/a
2	HEY1	chr1:214781044-214781562	K562	blood:	n/a	n/a
3	HEY1	chr1:214779710-214781017	K562	blood:	n/a	n/a
4	IRF1	chr1:214783174-214783214	K562	blood:	n/a	n/a
5	POLR2A	chr1:214778834-214781903	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr1:214781525-214781879	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr1:214781028-214781036	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr1:214780684-214781195	K562	blood:	n/a	n/a
9	POLR2A	chr1:214779702-214780883	GM12878	blood:	n/a	n/a
10	POLR2A	chr1:214781118-214782038	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr1:214780707-214781206	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr1:214782507-214782527	HepG2	liver:	n/a	n/a
13	POLR2A	chr1:214782585-214782637	HepG2	liver:	n/a	n/a
14	POLR2A	chr1:214779788-214780953	GM12878	blood:	n/a	n/a
15	POLR2A	chr1:214781214-214781523	K562	blood:	n/a	n/a
16	POLR2A	chr1:214779708-214782066	GM12892	blood:	n/a	n/a
17	POLR2A	chr1:214782270-214782501	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr1:214780900-214781017	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr1:214782721-214782726	HepG2	liver:	n/a	n/a
20	POLR2A	chr1:214780363-214781117	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr1:214780975-214782007	GM12878	blood:	n/a	n/a
22	POLR2A	chr1:214781712-214781956	K562	blood:	n/a	n/a
23	POLR2A	chr1:214782560-214783228	K562	blood:	n/a	n/a
24	POLR2A	chr1:214779700-214782190	GM12878	blood:	n/a	n/a
25	POLR2A	chr1:214782228-214782454	GM12878	blood:	n/a	n/a
26	POLR2A	chr1:214781717-214782039	K562	blood:	n/a	n/a
27	POLR2A	chr1:214779081-214782186	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr1:214778892-214782541	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr1:214781118-214781223	HepG2	liver:	n/a	n/a
30	POLR2A	chr1:214781086-214782058	GM12878	blood:	n/a	n/a
31	POLR2A	chr1:214780855-214781187	A549	lung:	n/a	n/a
32	POLR2A	chr1:214781622-214781786	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr1:214780671-214782077	K562	blood:	n/a	n/a
34	POLR2A	chr1:214782266-214782475	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr1:214781612-214782520	A549	lung:	n/a	n/a
36	RCOR1	chr1:214783130-214783286	K562	blood:	n/a	n/a
37	STAT3	chr1:214783001-214783121	MCF10A-Er-Src	breast:	n/a	n/a
38	ZNF384	chr1:214783639-214783972	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:214781904-214781954	ProgFib	skin:	n/a
2	chr1:214781904-214781954	ProgFib	skin:	n/a
3	chr1:214782555-214782605	BJ	skin:	n/a
4	chr1:214780880-214780930	HRCEpiC	kidney:	n/a
5	chr1:214781663-214781713	HRPEpiC	eye:	n/a
6	chr1:214782434-214782484	Jurkat	blood:	n/a
7	chr1:214781904-214781954	HCF	heart:	n/a
8	chr1:214782555-214782605	MCF10A-Er-Src	breast:	n/a
9	chr1:214780880-214780930	ovcar-3	ovarian:	n/a
10	chr1:214780880-214780930	IMR90	lung:	fetal
11	chr1:214782654-214782704	AG09319	gingival:	n/a
12	chr1:214781663-214781713	HCT-116	colon:	n/a
13	chr1:214781663-214781713	GM12892	blood:	n/a
14	chr1:214781904-214781954	SK-N-SH	brain:	n/a
15	chr1:214782654-214782704	HRCEpiC	kidney:	n/a
16	chr1:214782654-214782704	HRPEpiC	eye:	n/a
17	chr1:214781456-214781506	AG04449	skin:	fetal
18	chr1:214781663-214781713	IMR90	lung:	fetal
19	chr1:214782654-214782704	Jurkat	blood:	n/a
20	chr1:214782434-214782484	AoSMC	blood vessel:	n/a
21	chr1:214781663-214781713	HCPEpiC	choroid plexus:	n/a
22	chr1:214781904-214781954	HAEpiC	amniotic membrane:	n/a
23	chr1:214782434-214782484	IMR90	lung:	fetal
24	chr1:214781904-214781954	AG09319	gingival:	n/a
25	chr1:214781456-214781506	SK-N-MC	brain:	n/a
26	chr1:214782555-214782605	NB4	blood:	n/a
27	chr1:214781663-214781713	K562	blood:	n/a
28	chr1:214782555-214782605	HCF	heart:	n/a
29	chr1:214782434-214782484	PANC-1	pancreas:	n/a
30	chr1:214781456-214781506	PANC-1	pancreas:	n/a
31	chr1:214781904-214781954	AG10803	skin:	n/a
32	chr1:214780880-214780930	AG04449	skin:	fetal
33	chr1:214780880-214780930	NT2-D1	testis:	n/a
34	chr1:214782555-214782605	T-47D	breast:	n/a
35	chr1:214781904-214781954	NH-A	brain:	n/a
36	chr1:214782555-214782605	BE2_C	brain:	n/a
37	chr1:214780880-214780930	HMEC	breast:	n/a
38	chr1:214780880-214780930	AG09309	skin:	n/a
39	chr1:214780880-214780930	GM19239	blood:	n/a
40	chr1:214781904-214781954	U87	brain:	n/a
41	chr1:214782434-214782484	HNPCEpiC	eye:	n/a
42	chr1:214781456-214781506	H1-hESC	embryonic stem cell:	embryo
43	chr1:214781663-214781713	SKMC	muscle:	n/a
44	chr1:214782434-214782484	HL-60	blood:	n/a
45	chr1:214781663-214781713	LNCaP	prostate:	n/a
46	chr1:214781904-214781954	SAEC	small airway:	n/a
47	chr1:214782434-214782484	NH-A	brain:	n/a
48	chr1:214781456-214781506	HRE	kidney:	n/a
49	chr1:214782654-214782704	HMEC	breast:	n/a
50	chr1:214781456-214781506	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:214774784..214777425-chr1:214779446..214783969,6	K562	blood:

No data

Variant related genes	Relation type
ABHD17AP3	TF binding region
ABHD17AP3	CpG island
ENSG00000117724	chromatin interactions

Extended variants
information (count: 118 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:118 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112713739	chr1:214780932-214780933	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs553505005	chr1:214780936-214780937	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573337139	chr1:214780951-214780952	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545652413	chr1:214780995-214780996	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs565568731	chr1:214781027-214781028	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs539765785	chr1:214781050-214781051	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs531279008	chr1:214781053-214781054	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543395740	chr1:214781054-214781055	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184355748	chr1:214781069-214781070	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189099920	chr1:214781093-214781094	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548824863	chr1:214781168-214781169	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs181722684	chr1:214781187-214781188	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184741075	chr1:214781264-214781265	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531600200	chr1:214781296-214781297	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551199373	chr1:214781342-214781343	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571165371	chr1:214781353-214781354	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536959928	chr1:214781356-214781357	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550528480	chr1:214781359-214781360	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567574511	chr1:214781401-214781402	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs139285179	chr1:214781443-214781444	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372407537	chr1:214781457-214781458	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150010650	chr1:214781515-214781516	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189965200	chr1:214781574-214781575	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375466739	chr1:214781584-214781585	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377186475	chr1:214781588-214781589	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369653084	chr1:214781597-214781598	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570636025	chr1:214781619-214781620	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs373999452	chr1:214781626-214781627	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573533537	chr1:214781650-214781651	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs28391086	chr1:214781685-214781686	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs559172003	chr1:214781706-214781707	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528179607	chr1:214781723-214781724	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556539205	chr1:214781725-214781726	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539692349	chr1:214781748-214781749	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551123181	chr1:214781766-214781767	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564755615	chr1:214781789-214781790	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530690137	chr1:214781807-214781808	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550580192	chr1:214781811-214781812	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567586937	chr1:214781820-214781821	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536242062	chr1:214781841-214781842	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547019667	chr1:214781842-214781843	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566923886	chr1:214781870-214781871	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539143852	chr1:214781885-214781886	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559159933	chr1:214781891-214781892	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs575930621	chr1:214781892-214781893	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs552867553	chr1:214781927-214781928	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs538467241	chr1:214781942-214781943	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs267598366	chr1:214781961-214781962	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs180811596	chr1:214781971-214781972	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs186158039	chr1:214781988-214781989	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22522925	CNVD
Primary hepatocellular	22912832	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214777600-214782600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:214777600-214800400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:214777600-214810800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:214777600-214838600	Weak transcription	Esophagus	oesophagus
5	chr1:214777800-214781000	Weak transcription	Fetal Muscle Leg	muscle
6	chr1:214777800-214838400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:214778000-214839200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:214778200-214781000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr1:214778200-214782400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:214778200-214782600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr1:214778200-214782600	Weak transcription	Fetal Lung	lung
12	chr1:214778200-214783000	Weak transcription	Fetal Kidney	kidney
13	chr1:214778200-214786600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:214778200-214786600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr1:214778200-214791200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:214778200-214791200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:214778200-214793000	Weak transcription	HSMM	muscle
18	chr1:214778200-214793600	Weak transcription	Duodenum Mucosa	Duodenum
19	chr1:214778200-214793800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:214778200-214803600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr1:214778400-214781800	Weak transcription	K562	blood
22	chr1:214778400-214786600	Weak transcription	Osteobl	bone
23	chr1:214778400-214786800	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr1:214778400-214794200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:214778600-214782400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr1:214778600-214782600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:214778600-214782600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr1:214778600-214788000	Weak transcription	Hela-S3	cervix
29	chr1:214778600-214791200	Weak transcription	NHEK	skin
30	chr1:214778800-214781400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:214778800-214782600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:214778800-214782600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:214778800-214782600	Weak transcription	HUVEC	blood vessel
34	chr1:214778800-214782800	Weak transcription	Fetal Brain Female	brain
35	chr1:214778800-214783200	Strong transcription	H1 Cell Line	embryonic stem cell
36	chr1:214778800-214783200	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr1:214778800-214783400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr1:214778800-214783600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:214778800-214786000	Weak transcription	NHDF-Ad	bronchial
40	chr1:214778800-214786600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr1:214778800-214787600	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr1:214778800-214787800	Weak transcription	HepG2	liver
43	chr1:214778800-214788800	Weak transcription	HMEC	breast
44	chr1:214778800-214794000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr1:214779000-214781800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr1:214779000-214782800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:214779000-214783200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:214779200-214781000	Genic enhancers	Dnd41	blood
49	chr1:214779200-214783000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:214779400-214781200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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