Variant report

Variant	nsv1049259
Chromosome Location	chr10:49901984-49924310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr10:49907467-49907538	GM12878	blood:	n/a	n/a
2	BHLHE40	chr10:49909241-49909921	GM12878	blood:	n/a	n/a
3	CEBPB	chr10:49922071-49922254	K562	blood:	n/a	n/a
4	CEBPB	chr10:49905312-49905528	HepG2	liver:	n/a	chr10:49905429-49905440
5	CEBPB	chr10:49905314-49905579	A549	lung:	n/a	chr10:49905429-49905440
6	CHD2	chr10:49903012-49903050	HepG2	liver:	n/a	n/a
7	CHD2	chr10:49906613-49906679	GM12878	blood:	n/a	n/a
8	CHD2	chr10:49907101-49907552	GM12878	blood:	n/a	n/a
9	CHD2	chr10:49902816-49902891	GM12878	blood:	n/a	n/a
10	CTCF	chr10:49909300-49909450	NB4	blood:	n/a	n/a
11	CTCF	chr10:49909293-49909470	Spleen_OC	spleen:	n/a	n/a
12	CTCF	chr10:49909330-49909457	GM13976	blood:	n/a	n/a
13	CTCF	chr10:49909260-49909410	HMF	breast:	n/a	n/a
14	CTCF	chr10:49906488-49906677	GM12891	blood:	n/a	n/a
15	CTCF	chr10:49906460-49906610	GM12875	blood:	n/a	n/a
16	CTCF	chr10:49909220-49909470	Caco-2	colon:	n/a	n/a
17	CTCF	chr10:49906500-49906650	GM12869	blood:	n/a	n/a
18	CTCF	chr10:49909333-49909491	K562	blood:	n/a	n/a
19	CTCF	chr10:49906485-49906747	GM12892	blood:	n/a	n/a
20	CTCF	chr10:49906480-49906630	GM12870	blood:	n/a	n/a
21	CTCF	chr10:49906440-49906590	GM12875	blood:	n/a	n/a
22	CTCF	chr10:49909340-49909490	GM12870	blood:	n/a	n/a
23	CTCF	chr10:49906580-49906730	GM12871	blood:	n/a	n/a
24	CTCF	chr10:49909390-49909462	GM20000	blood:	n/a	n/a
25	CTCF	chr10:49911664-49911684	GM20000	blood:	n/a	n/a
26	CTCF	chr10:49909280-49909430	GM12867	blood:	n/a	n/a
27	CTCF	chr10:49909320-49909470	GM12874	blood:	n/a	n/a
28	CTCF	chr10:49906560-49906595	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr10:49909260-49909410	GM12872	blood:	n/a	n/a
30	CTCF	chr10:49909360-49909510	GM12871	blood:	n/a	n/a
31	CTCF	chr10:49906464-49906738	K562	blood:	n/a	n/a
32	CTCF	chr10:49909300-49909450	GM12869	blood:	n/a	n/a
33	CTCF	chr10:49906602-49906609	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr10:49909260-49909410	GM12871	blood:	n/a	n/a
35	CTCF	chr10:49906500-49906650	HepG2	liver:	n/a	n/a
36	CTCF	chr10:49909200-49909350	RPTEC	kidney:	n/a	n/a
37	CTCF	chr10:49906520-49906670	GM12878	blood:	n/a	n/a
38	CTCF	chr10:49906520-49906670	GM12867	blood:	n/a	n/a
39	CTCF	chr10:49906546-49906678	GM13977	blood:	n/a	n/a
40	CTCF	chr10:49909366-49909435	GM19238	blood:	n/a	n/a
41	CTCF	chr10:49909280-49909430	GM12872	blood:	n/a	n/a
42	CTCF	chr10:49914040-49914190	GM12875	blood:	n/a	n/a
43	CTCF	chr10:49906500-49906650	GM06990	blood:	n/a	n/a
44	CTCF	chr10:49909310-49909487	GM19239	blood:	n/a	n/a
45	CTCF	chr10:49909364-49909437	GM19240	blood:	n/a	n/a
46	CTCF	chr10:49909260-49909410	GM12801	blood:	n/a	n/a
47	CTCF	chr10:49909320-49909470	GM12865	blood:	n/a	n/a
48	CTCF	chr10:49906520-49906670	GM12874	blood:	n/a	n/a
49	CTCF	chr10:49906520-49906670	GM06990	blood:	n/a	n/a
50	CTCF	chr10:49909560-49909710	GM12872	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49909285-49909335	NB4	blood:	n/a
2	chr10:49909285-49909335	Jurkat	blood:	n/a
3	chr10:49909285-49909335	SKMC	muscle:	n/a
4	chr10:49909285-49909335	HepG2	liver:	n/a
5	chr10:49909285-49909335	HEK293	kidney:	embryo
6	chr10:49909285-49909335	HCPEpiC	choroid plexus:	n/a
7	chr10:49909285-49909335	NHDF-neo	bronchial:	n/a
8	chr10:49909285-49909335	HCF	heart:	n/a
9	chr10:49909285-49909335	PrEC	prostate:	n/a
10	chr10:49909285-49909335	HRCEpiC	kidney:	n/a
11	chr10:49909285-49909335	LNCaP	prostate:	n/a
12	chr10:49909285-49909335	T-47D	breast:	n/a
13	chr10:49909285-49909335	Hepatocyte	liver:	n/a
14	chr10:49909285-49909335	ovcar-3	ovarian:	n/a
15	chr10:49909285-49909335	GM12891	blood:	n/a
16	chr10:49909285-49909335	NHBE	bronchial:	n/a
17	chr10:49909285-49909335	HRPEpiC	eye:	n/a
18	chr10:49909285-49909335	GM19239	blood:	n/a
19	chr10:49909285-49909335	BE2_C	brain:	n/a
20	chr10:49909285-49909335	AG09319	gingival:	n/a
21	chr10:49909285-49909335	HUVEC	blood vessel:	n/a
22	chr10:49909285-49909335	SAEC	small airway:	n/a
23	chr10:49909285-49909335	HMEC	breast:	n/a
24	chr10:49909285-49909335	AoSMC	blood vessel:	n/a
25	chr10:49909285-49909335	NT2-D1	testis:	n/a
26	chr10:49909285-49909335	AG04449	skin:	fetal
27	chr10:49909285-49909335	HCT-116	colon:	n/a
28	chr10:49909285-49909335	AG10803	skin:	n/a
29	chr10:49909285-49909335	MCF-7	breast:	n/a
30	chr10:49909285-49909335	Caco-2	colon:	n/a
31	chr10:49909285-49909335	GM12892	blood:	n/a
32	chr10:49909285-49909335	HRE	kidney:	n/a
33	chr10:49909285-49909335	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:49909285-49909335	PFSK-1	brain:	n/a
35	chr10:49909285-49909335	MCF10A-Er-Src	breast:	n/a
36	chr10:49909285-49909335	NH-A	brain:	n/a
37	chr10:49909285-49909335	HEEpiC	esophagus:	n/a
38	chr10:49909285-49909335	HAEpiC	amniotic membrane:	n/a
39	chr10:49909285-49909335	Hela-S3	cervix:	n/a
40	chr10:49909285-49909335	ProgFib	skin:	n/a
41	chr10:49909285-49909335	AG04450	lung:	fetal
42	chr10:49909285-49909335	AG09309	skin:	n/a
43	chr10:49909285-49909335	H1-hESC	embryonic stem cell:	embryo
44	chr10:49909285-49909335	CMK	blood:	n/a
45	chr10:49909285-49909335	HNPCEpiC	eye:	n/a
46	chr10:49909285-49909335	SK-N-MC	brain:	n/a
47	chr10:49909285-49909335	HCM	heart:	n/a
48	chr10:49909285-49909335	K562	blood:	n/a
49	chr10:49909285-49909335	SK-N-SH	brain:	n/a
50	chr10:49909285-49909335	BJ	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:49905425..49907287-chr10:49911171..49913733,2	MCF-7	breast:
2	chr10:49918859..49921517-chr10:49927615..49930107,2	MCF-7	breast:
3	chr10:49899844..49902277-chr10:50218756..50220878,2	MCF-7	breast:
4	chr10:49905321..49907163-chr10:49908758..49910587,2	K562	blood:
5	chr10:49905425..49907287-chr10:49911171..49913733,2	MCF-7	breast:
6	chr10:49906264..49908604-chr10:49911628..49913491,2	MCF-7	breast:
7	chr10:49907771..49909890-chr10:49911982..49914593,2	K562	blood:
8	chr10:49906264..49908604-chr10:49911628..49913491,2	MCF-7	breast:
9	chr10:49905321..49907163-chr10:49908758..49910587,2	K562	blood:
10	chr10:49912829..49914750-chr10:49915625..49918084,2	K562	blood:
11	chr10:49895299..49896827-chr10:49902202..49904917,2	MCF-7	breast:
12	chr10:49907771..49909890-chr10:49911982..49914593,2	K562	blood:

No data

Variant related genes	Relation type
WDFY4	TF binding region
WDFY4	CpG island
ENSG00000128815	chromatin interactions

Extended variants
information (count: 945 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:945 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570553622	chr10:49902004-49902005	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375501584	chr10:49902007-49902008	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72787281	chr10:49902018-49902019	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs181115191	chr10:49902033-49902034	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139236768	chr10:49902070-49902071	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1004407	chr10:49902125-49902126	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs545437534	chr10:49902126-49902127	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184834324	chr10:49902130-49902131	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563605023	chr10:49902141-49902142	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189339485	chr10:49902158-49902159	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs180783972	chr10:49902159-49902160	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561174630	chr10:49902188-49902189	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573270001	chr10:49902194-49902195	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs3923678	chr10:49902197-49902198	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs546517248	chr10:49902198-49902199	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534807029	chr10:49902210-49902211	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564522623	chr10:49902236-49902237	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531946728	chr10:49902238-49902239	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550570861	chr10:49902270-49902271	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568820448	chr10:49902275-49902276	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185445640	chr10:49902298-49902299	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142453340	chr10:49902331-49902332	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4293051	chr10:49902374-49902375	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567887809	chr10:49902391-49902392	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4012685	chr10:49902402-49902403	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs4012686	chr10:49902408-49902409	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs12764199	chr10:49902422-49902423	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376702483	chr10:49902433-49902434	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538611185	chr10:49902464-49902465	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557331482	chr10:49902466-49902467	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575637510	chr10:49902467-49902468	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557783294	chr10:49902480-49902481	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543151258	chr10:49902487-49902488	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533132982	chr10:49902500-49902501	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554318916	chr10:49902507-49902508	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572735859	chr10:49902517-49902518	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540053361	chr10:49902539-49902540	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373740707	chr10:49902551-49902552	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564808806	chr10:49902557-49902558	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191026571	chr10:49902604-49902605	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181932178	chr10:49902610-49902611	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186818616	chr10:49902650-49902651	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529733081	chr10:49902663-49902664	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74749028	chr10:49902666-49902667	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74525850	chr10:49902667-49902668	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577741468	chr10:49902692-49902693	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548300421	chr10:49902710-49902711	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539937427	chr10:49902725-49902726	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566591008	chr10:49902737-49902738	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143874815	chr10:49902738-49902739	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Schizophrenia	23813976	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	16272173	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49895200-49904200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:49895200-49906200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr10:49897000-49918200	Genic enhancers	Primary B cells from peripheral blood	blood
4	chr10:49897400-49903200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr10:49899600-49903800	Weak transcription	Spleen	Spleen
6	chr10:49900200-49908600	Weak transcription	Colonic Mucosa	Colon
7	chr10:49900400-49902800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr10:49900400-49906600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr10:49900800-49906800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr10:49900800-49908800	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr10:49901000-49902800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr10:49901200-49903000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr10:49901400-49902400	Weak transcription	GM12878-XiMat	blood
14	chr10:49901600-49902400	Strong transcription	Primary B cells from cord blood	blood
15	chr10:49901600-49907200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:49902200-49903400	Enhancers	Fetal Muscle Leg	muscle
17	chr10:49902200-49907000	Weak transcription	Right Atrium	heart
18	chr10:49902400-49903400	Enhancers	GM12878-XiMat	blood
19	chr10:49902400-49904200	Genic enhancers	Primary B cells from cord blood	blood
20	chr10:49902400-49906000	Weak transcription	Fetal Thymus	thymus
21	chr10:49902600-49903200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr10:49902800-49903800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr10:49902800-49905400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr10:49903000-49903800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr10:49903200-49903600	Strong transcription	Primary hematopoietic stem cells	blood
26	chr10:49903400-49903600	Enhancers	Right Ventricle	heart
27	chr10:49903400-49903800	Flanking Active TSS	GM12878-XiMat	blood
28	chr10:49903400-49907400	Weak transcription	Fetal Muscle Leg	muscle
29	chr10:49903600-49904400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr10:49903600-49905800	Weak transcription	Right Ventricle	heart
31	chr10:49903800-49904200	Enhancers	GM12878-XiMat	blood
32	chr10:49903800-49904400	Genic enhancers	Spleen	Spleen
33	chr10:49903800-49907400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr10:49903800-49911400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr10:49904200-49904400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr10:49904200-49906800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr10:49904200-49907000	Strong transcription	Primary B cells from cord blood	blood
38	chr10:49904200-49909600	Genic enhancers	GM12878-XiMat	blood
39	chr10:49904400-49904800	Strong transcription	Spleen	Spleen
40	chr10:49904400-49906800	Strong transcription	Primary hematopoietic stem cells	blood
41	chr10:49904800-49905800	Weak transcription	Spleen	Spleen
42	chr10:49905400-49905800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
43	chr10:49905800-49906200	Enhancers	Right Ventricle	heart
44	chr10:49905800-49907600	Strong transcription	Primary neutrophils fromperipheralblood	blood
45	chr10:49905800-49907600	Enhancers	Left Ventricle	heart
46	chr10:49905800-49908200	Strong transcription	Spleen	Spleen
47	chr10:49906000-49907200	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr10:49906000-49907800	Enhancers	Fetal Heart	heart
49	chr10:49906000-49909000	Enhancers	Fetal Thymus	thymus
50	chr10:49906200-49906400	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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