Variant report

Variant	esv1850613
Chromosome Location	chr10:51393995-51501515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:794)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 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	chr10:51498525-51498807	HepG2	liver:	n/a	n/a
2	ATF1	chr10:51493021-51493256	K562	blood:	n/a	n/a
3	BACH1	chr10:51497179-51497372	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:51488208-51489253	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:51488154-51489051	K562	blood:	n/a	n/a
6	BCL11A	chr10:51477990-51478142	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:51501363-51501407	K562	blood:	n/a	n/a
8	BHLHE40	chr10:51488172-51489419	K562	blood:	n/a	chr10:51489310-51489326
9	BHLHE40	chr10:51500736-51501099	K562	blood:	n/a	n/a
10	BRCA1	chr10:51500821-51501021	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr10:51496898-51497079	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr10:51488737-51489298	K562	blood:	n/a	n/a
13	CCNT2	chr10:51488785-51489504	K562	blood:	n/a	n/a
14	CEBPB	chr10:51495776-51496002	H1-hESC	embryonic stem cell:	n/a	chr10:51495870-51495881
15	CEBPB	chr10:51495708-51496045	IMR90	lung:	n/a	chr10:51495870-51495881
16	CEBPB	chr10:51495728-51496020	Hela-S3	cervix:	n/a	chr10:51495870-51495881
17	CEBPB	chr10:51495788-51495959	ECC-1	luminal epithelium:	n/a	chr10:51495870-51495881
18	CEBPB	chr10:51495783-51495916	HepG2	liver:	n/a	chr10:51495870-51495881
19	CEBPB	chr10:51500891-51500985	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr10:51500840-51501123	HepG2	liver:	n/a	n/a
21	CEBPB	chr10:51500916-51501060	K562	blood:	n/a	n/a
22	CEBPB	chr10:51397664-51397920	K562	blood:	n/a	n/a
23	CEBPB	chr10:51495736-51495938	HepG2	liver:	n/a	chr10:51495870-51495881
24	CEBPB	chr10:51495703-51496065	HepG2	liver:	n/a	chr10:51495870-51495881
25	CEBPB	chr10:51495750-51495957	MCF-7	breast:	n/a	chr10:51495870-51495881
26	CHD2	chr10:51488692-51489092	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr10:51488874-51489021	HepG2	liver:	n/a	n/a
28	CHD2	chr10:51488854-51489026	K562	blood:	n/a	n/a
29	CREB1	chr10:51488748-51489318	A549	lung:	n/a	n/a
30	CTCF	chr10:51499520-51499670	K562	blood:	n/a	chr10:51499642-51499650
31	CTCF	chr10:51497044-51497248	K562	blood:	n/a	chr10:51497141-51497162 chr10:51497146-51497164 chr10:51497149-51497159 chr10:51497145-51497158
32	CTCF	chr10:51497120-51497270	GM12871	blood:	n/a	chr10:51497141-51497162 chr10:51497146-51497164 chr10:51497149-51497159 chr10:51497145-51497158
33	CTCF	chr10:51499540-51499690	HepG2	liver:	n/a	chr10:51499642-51499650
34	CTCF	chr10:51488820-51488970	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr10:51488942-51489098	Fibrobl	skin:	n/a	n/a
36	CTCF	chr10:51488880-51489030	GM12874	blood:	n/a	n/a
37	CTCF	chr10:51488975-51489189	Lung_OC	lung:	n/a	n/a
38	CTCF	chr10:51488840-51488990	HepG2	liver:	n/a	n/a
39	CTCF	chr10:51488880-51489030	MCF-7	breast:	n/a	n/a
40	CTCF	chr10:51488780-51489030	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr10:51485991-51486385	K562	blood:	n/a	n/a
42	CTCF	chr10:51497040-51497190	HEK293	kidney:	n/a	chr10:51497141-51497162 chr10:51497146-51497164 chr10:51497149-51497159 chr10:51497145-51497158
43	CTCF	chr10:51497154-51497186	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:51488780-51488930	HEK293	kidney:	n/a	n/a
45	CTCF	chr10:51489080-51489230	HepG2	liver:	n/a	n/a
46	CTCF	chr10:51488840-51488990	HAc	cerebellar:	n/a	n/a
47	CTCF	chr10:51488880-51489030	HMEC	breast:	n/a	n/a
48	CTCF	chr10:51496996-51497294	K562	blood:	n/a	chr10:51497141-51497162 chr10:51497146-51497164 chr10:51497149-51497159 chr10:51497145-51497158
49	CTCF	chr10:51488950-51489130	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr10:51497020-51497296	K562	blood:	n/a	chr10:51497141-51497162 chr10:51497146-51497164 chr10:51497149-51497159 chr10:51497145-51497158

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:51489980-51490030	HCF	heart:	n/a
2	chr10:51489980-51490030	HCF	heart:	n/a
3	chr10:51487558-51487608	SAEC	small airway:	n/a
4	chr10:51489980-51490030	NHDF-neo	bronchial:	n/a
5	chr10:51491984-51492034	GM12878	blood:	n/a
6	chr10:51465444-51465494	GM12878	blood:	n/a
7	chr10:51489643-51489693	GM12878	blood:	n/a
8	chr10:51463156-51463206	BJ	skin:	n/a
9	chr10:51487759-51487809	U87	brain:	n/a
10	chr10:51487759-51487809	LNCaP	prostate:	n/a
11	chr10:51491984-51492034	HEK293	kidney:	embryo
12	chr10:51487635-51487685	NB4	blood:	n/a
13	chr10:51461855-51461905	HAEpiC	amniotic membrane:	n/a
14	chr10:51461855-51461905	U87	brain:	n/a
15	chr10:51487558-51487608	AG04449	skin:	fetal
16	chr10:51461855-51461905	AG10803	skin:	n/a
17	chr10:51468217-51468267	NT2-D1	testis:	n/a
18	chr10:51489980-51490030	BE2_C	brain:	n/a
19	chr10:51489223-51489273	HMEC	breast:	n/a
20	chr10:51488973-51489023	HCT-116	colon:	n/a
21	chr10:51468217-51468267	SAEC	small airway:	n/a
22	chr10:51489643-51489693	HUVEC	blood vessel:	n/a
23	chr10:51468217-51468267	PrEC	prostate:	n/a
24	chr10:51487759-51487809	Hela-S3	cervix:	n/a
25	chr10:51489510-51489560	HUVEC	blood vessel:	n/a
26	chr10:51461855-51461905	SK-N-SH	brain:	n/a
27	chr10:51487759-51487809	HRE	kidney:	n/a
28	chr10:51463156-51463206	SAEC	small airway:	n/a
29	chr10:51465444-51465494	GM12891	blood:	n/a
30	chr10:51487635-51487685	SK-N-SH_RA	brain:	n/a
31	chr10:51463156-51463206	ovcar-3	ovarian:	n/a
32	chr10:51489980-51490030	LNCaP	prostate:	n/a
33	chr10:51487635-51487685	CMK	blood:	n/a
34	chr10:51487759-51487809	AG10803	skin:	n/a
35	chr10:51461855-51461905	HCF	heart:	n/a
36	chr10:51487759-51487809	HCPEpiC	choroid plexus:	n/a
37	chr10:51491984-51492034	HL-60	blood:	n/a
38	chr10:51489510-51489560	SK-N-SH	brain:	n/a
39	chr10:51489643-51489693	Caco-2	colon:	n/a
40	chr10:51463156-51463206	SK-N-SH	brain:	n/a
41	chr10:51461855-51461905	ovcar-3	ovarian:	n/a
42	chr10:51465444-51465494	Caco-2	colon:	n/a
43	chr10:51489643-51489693	LNCaP	prostate:	n/a
44	chr10:51489223-51489273	SK-N-SH	brain:	n/a
45	chr10:51488973-51489023	SK-N-SH	brain:	n/a
46	chr10:51491984-51492034	HUVEC	blood vessel:	n/a
47	chr10:51489643-51489693	AG09309	skin:	n/a
48	chr10:51487759-51487809	AG04450	lung:	fetal
49	chr10:51468217-51468267	Hela-S3	cervix:	n/a
50	chr10:51489980-51490030	BJ	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:47637552..47640564-chr10:51501175..51503678,3	MCF-7	breast:
2	chr10:51488667..51489638-chr19:9250701..9251449,2	NB4	blood:
3	chr10:47654251..47654891-chr10:51488416..51489496,4	Hela-S3	cervix:
4	chr10:47653740..47654385-chr10:51488816..51489933,3	MCF-7	breast:
5	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
6	chr10:51498114..51501016-chr10:51502450..51504451,2	MCF-7	breast:
7	chr10:47653734..47654656-chr10:51488800..51489544,4	MCF-7	breast:
8	chr10:51489258..51491268-chr10:51531426..51533100,2	MCF-7	breast:
9	chr10:47654274..47658037-chr10:51487059..51489810,4	K562	blood:
10	chr10:47654140..47654870-chr10:51488638..51489755,11	HCT-116	colon:
11	chr10:51487738..51490469-chr10:51490768..51492273,2	MCF-7	breast:
12	chr10:47654306..47654893-chr10:51488919..51489481,3	MCF-7	breast:
13	chr10:51497870..51501630-chr10:51543327..51546015,3	MCF-7	breast:
14	chr10:47652879..47654869-chr10:51487976..51491279,3	MCF-7	breast:
15	chr10:47652235..47655869-chr10:51487775..51491801,8	MCF-7	breast:

No data

Variant related genes	Relation type
AGAP7	TF binding region
AGAP7	CpG island
ENSG00000198250	chromatin interactions
ENSG00000228326	chromatin interactions
ENSG00000259942	chromatin interactions
ENSG00000130803	chromatin interactions

Extended variants
information (count: 970 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:970 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544517467	chr10:51461806-51461807	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs79489567	chr10:51461808-51461809	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs529950092	chr10:51461825-51461826	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs75074999	chr10:51461838-51461839	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs79368032	chr10:51461859-51461860	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs377626318	chr10:51461870-51461871	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs191638130	chr10:51461884-51461885	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs183153884	chr10:51461885-51461886	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs539730315	chr10:51461927-51461928	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs187107924	chr10:51461950-51461951	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs570446028	chr10:51461993-51461994	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs549703743	chr10:51462016-51462017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537412607	chr10:51462048-51462049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557256805	chr10:51462103-51462104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569189778	chr10:51462128-51462129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536486276	chr10:51462129-51462130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377458288	chr10:51462152-51462153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554738154	chr10:51462188-51462189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2611480	chr10:51462264-51462265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372370862	chr10:51462454-51462455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371687108	chr10:51462546-51462547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540730751	chr10:51462557-51462558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200470358	chr10:51462599-51462600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373623396	chr10:51462626-51462627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577197045	chr10:51462658-51462659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544265010	chr10:51462699-51462700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs28576473	chr10:51462703-51462704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201615174	chr10:51462763-51462764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530014642	chr10:51462774-51462775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570697274	chr10:51462803-51462804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61850061	chr10:51462855-51462856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542101426	chr10:51462861-51462862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560400744	chr10:51462866-51462867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527463489	chr10:51462867-51462868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541826162	chr10:51462880-51462881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377171448	chr10:51462915-51462916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375032925	chr10:51462948-51462949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564001288	chr10:51462965-51462966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555841960	chr10:51462971-51462972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549355141	chr10:51462975-51462976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374130340	chr10:51462991-51462992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371175214	chr10:51462992-51462993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569255911	chr10:51463030-51463031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536550064	chr10:51463106-51463107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11816557	chr10:51463107-51463108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548433587	chr10:51463108-51463109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182335857	chr10:51463124-51463125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534110013	chr10:51463129-51463130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11817836	chr10:51463139-51463140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186665637	chr10:51463157-51463158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
Autism	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	21935476	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51461800-51462000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:51462000-51467000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:51464000-51466400	Weak transcription	Thymus	Thymus
4	chr10:51486600-51488200	Weak transcription	Right Atrium	heart
5	chr10:51486600-51488800	Weak transcription	Lung	lung
6	chr10:51487400-51487600	Enhancers	Primary B cells from peripheral blood	blood
7	chr10:51487400-51488200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr10:51487600-51487800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:51487600-51487800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:51487600-51487800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
11	chr10:51487600-51488000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
12	chr10:51487600-51488000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr10:51487600-51488000	Enhancers	Gastric	stomach
14	chr10:51487600-51488000	Enhancers	K562	blood
15	chr10:51487600-51488200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr10:51487600-51488200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:51487600-51488200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr10:51487600-51488200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr10:51487600-51488200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr10:51487600-51488200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr10:51487600-51488200	Enhancers	Fetal Thymus	thymus
22	chr10:51487600-51488200	Enhancers	Pancreas	Pancrea
23	chr10:51487600-51488200	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr10:51487600-51488200	Enhancers	Thymus	Thymus
25	chr10:51487600-51488400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
26	chr10:51487600-51488400	Bivalent Enhancer	HepG2	liver
27	chr10:51487600-51488800	Enhancers	Spleen	Spleen
28	chr10:51487800-51488400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr10:51488000-51488200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr10:51488000-51488200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr10:51488000-51488200	Enhancers	Hela-S3	cervix
32	chr10:51488000-51488400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr10:51488000-51488400	Weak transcription	Gastric	stomach
34	chr10:51488200-51488400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
35	chr10:51488200-51488400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
36	chr10:51488200-51488400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr10:51488200-51488400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
38	chr10:51488200-51488400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr10:51488200-51488400	Bivalent Enhancer	Primary B cells from cord blood	blood
40	chr10:51488200-51488400	Enhancers	Primary T cells from cord blood	blood
41	chr10:51488200-51488400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
42	chr10:51488200-51488400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr10:51488200-51488400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr10:51488200-51488400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr10:51488200-51488400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr10:51488200-51488400	Enhancers	Brain Cingulate Gyrus	brain
47	chr10:51488200-51488400	Bivalent Enhancer	Brain Germinal Matrix	brain
48	chr10:51488200-51488400	Bivalent Enhancer	Colon Smooth Muscle	Colon
49	chr10:51488200-51488400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
50	chr10:51488200-51488400	Bivalent Enhancer	Fetal Brain Female	brain

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