Variant report

Variant	nsv516275
Chromosome Location	chr10:26896432-26968171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:575)
CpG islands
(count:919)
Chromatin interactive
region (count:22)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:26964570-26964881	K562	blood:	n/a	n/a
2	ATF2	chr10:26917389-26917782	GM12878	blood:	n/a	n/a
3	ATF2	chr10:26917400-26917850	GM12878	blood:	n/a	n/a
4	ATF3	chr10:26954068-26954353	K562	blood:	n/a	n/a
5	ATF3	chr10:26926570-26926744	K562	blood:	n/a	chr10:26926582-26926591
6	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
8	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
9	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
10	BATF	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:26963417-26963432	K562	blood:	n/a	n/a
13	BHLHE40	chr10:26962966-26962980	K562	blood:	n/a	n/a
14	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
16	BRCA1	chr10:26952423-26952612	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr10:26964318-26964954	K562	blood:	n/a	n/a
18	CEBPB	chr10:26954005-26954489	K562	blood:	n/a	chr10:26954199-26954210
19	CEBPB	chr10:26961963-26962220	IMR90	lung:	n/a	chr10:26962123-26962134
20	CEBPB	chr10:26954017-26954298	K562	blood:	n/a	chr10:26954199-26954210
21	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
22	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
23	CEBPB	chr10:26954017-26954389	A549	lung:	n/a	chr10:26954199-26954210
24	CEBPB	chr10:26967830-26968049	K562	blood:	n/a	n/a
25	CEBPB	chr10:26954081-26954382	H1-hESC	embryonic stem cell:	n/a	chr10:26954199-26954210
26	CEBPB	chr10:26961963-26962323	K562	blood:	n/a	chr10:26962123-26962134
27	CEBPB	chr10:26967853-26968029	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:26946966-26947172	K562	blood:	n/a	n/a
30	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
31	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
32	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
33	CEBPB	chr10:26954028-26954383	IMR90	lung:	n/a	chr10:26954199-26954210
34	CEBPB	chr10:26954040-26954379	HepG2	liver:	n/a	chr10:26954199-26954210
35	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
36	CEBPB	chr10:26946921-26947139	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:26962043-26962214	HepG2	liver:	n/a	chr10:26962123-26962134
38	CEBPD	chr10:26954260-26954812	K562	blood:	n/a	n/a
39	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr10:26955538-26955614	K562	blood:	n/a	n/a
41	CTCF	chr10:26946458-26946503	LNCaP	prostate:	n/a	n/a
42	CTCF	chr10:26916360-26916510	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr10:26916320-26916470	GM12868	blood:	n/a	n/a
44	CTCF	chr10:26934800-26934950	GM12865	blood:	n/a	n/a
45	CTCF	chr10:26916320-26916470	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr10:26936662-26936814	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr10:26936600-26936750	GM12875	blood:	n/a	n/a
48	CTCF	chr10:26934923-26934938	LNCaP	prostate:	n/a	n/a
49	CTCF	chr10:26916340-26916490	GM12872	blood:	n/a	n/a
50	CTCF	chr10:26936813-26936814	GM19240	blood:	n/a	n/a

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26942225-26942275	HIPEpiC	eye:	n/a
2	chr10:26931978-26932028	GM19239	blood:	n/a
3	chr10:26911186-26911236	GM06990	blood:	n/a
4	chr10:26931991-26932041	HRCEpiC	kidney:	n/a
5	chr10:26942225-26942275	HIPEpiC	eye:	n/a
6	chr10:26931978-26932028	GM19239	blood:	n/a
7	chr10:26911186-26911236	GM06990	blood:	n/a
8	chr10:26931991-26932041	HRCEpiC	kidney:	n/a
9	chr10:26931926-26931976	IMR90	lung:	fetal
10	chr10:26931794-26931844	HNPCEpiC	eye:	n/a
11	chr10:26942225-26942275	HL-60	blood:	n/a
12	chr10:26932057-26932107	NHBE	bronchial:	n/a
13	chr10:26931794-26931844	HCF	heart:	n/a
14	chr10:26942165-26942215	HepG2	liver:	n/a
15	chr10:26930863-26930913	Hepatocyte	liver:	n/a
16	chr10:26932036-26932086	Jurkat	blood:	n/a
17	chr10:26932057-26932107	HAEpiC	amniotic membrane:	n/a
18	chr10:26942165-26942215	HEK293	kidney:	embryo
19	chr10:26932036-26932086	NT2-D1	testis:	n/a
20	chr10:26931912-26931962	GM12878	blood:	n/a
21	chr10:26932036-26932086	HRCEpiC	kidney:	n/a
22	chr10:26931912-26931962	BJ	skin:	n/a
23	chr10:26931794-26931844	HEK293	kidney:	embryo
24	chr10:26932036-26932086	HIPEpiC	eye:	n/a
25	chr10:26931991-26932041	Jurkat	blood:	n/a
26	chr10:26931991-26932041	HCF	heart:	n/a
27	chr10:26911186-26911236	K562	blood:	n/a
28	chr10:26931986-26932036	MCF10A-Er-Src	breast:	n/a
29	chr10:26931991-26932041	HIPEpiC	eye:	n/a
30	chr10:26931731-26931781	GM12878	blood:	n/a
31	chr10:26931912-26931962	PANC-1	pancreas:	n/a
32	chr10:26930863-26930913	SK-N-MC	brain:	n/a
33	chr10:26942225-26942275	HMEC	breast:	n/a
34	chr10:26931986-26932036	GM19239	blood:	n/a
35	chr10:26931978-26932028	PANC-1	pancreas:	n/a
36	chr10:26931978-26932028	K562	blood:	n/a
37	chr10:26932036-26932086	HRPEpiC	eye:	n/a
38	chr10:26911451-26911501	SKMC	muscle:	n/a
39	chr10:26931991-26932041	HCT-116	colon:	n/a
40	chr10:26931969-26932019	NHDF-neo	bronchial:	n/a
41	chr10:26911186-26911236	HCM	heart:	n/a
42	chr10:26930863-26930913	T-47D	breast:	n/a
43	chr10:26931794-26931844	AoSMC	blood vessel:	n/a
44	chr10:26911186-26911236	PFSK-1	brain:	n/a
45	chr10:26930863-26930913	U87	brain:	n/a
46	chr10:26931986-26932036	HIPEpiC	eye:	n/a
47	chr10:26930863-26930913	H1-hESC	embryonic stem cell:	embryo
48	chr10:26931986-26932036	GM12878	blood:	n/a
49	chr10:26931991-26932041	GM12878	blood:	n/a
50	chr10:26932057-26932107	SK-N-MC	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
2	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
3	chr10:26955921..26958837-chr10:26961876..26965160,3	K562	blood:
4	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:
5	chr10:26965108..26970102-chr10:26984839..26987979,6	K562	blood:
6	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
7	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
8	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
9	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
10	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
11	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
12	chr10:26954305..26956450-chr10:26987430..26988975,2	K562	blood:
13	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
14	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:
15	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
16	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
17	chr10:26953025..26955897-chr10:26956336..26959208,3	K562	blood:
18	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
19	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
20	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:
21	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
22	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDSS1-1	chr10:26933843-26933945	XLOC_008421
2	lnc-APBB1IP-3	chr10:26920245-26920348	NONHSAT011843
3	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011841
4	lnc-PDSS1-1	chr10:26941994-26942040	ENSG00000231976
5	lnc-ABI1-8	chr10:26907771-26907906	NONHSAT011842
6	lnc-PDSS1-1	chr10:26939483-26939691	NONHSAT011840
7	lnc-ABI1-8	chr10:26907771-26907837	l_271_chr10:26906510-26908315_testes
8	lnc-ABI1-8	chr10:26908129-26908315	l_271_chr10:26906510-26908315_testes
9	lnc-ABI1-8	chr10:26906511-26906782	l_271_chr10:26906510-26908315_testes
10	lnc-PDSS1-1	chr10:26938261-26938522	ENSG00000231976
11	lnc-PDSS1-1	chr10:26932157-26932525	XLOC_008421
12	lnc-PDSS1-1	chr10:26939483-26939586	ENSG00000231976
13	lnc-ABI1-1	chr10:26953135-26953321	ENSG00000227932.1
14	lnc-APBB1IP-3	chr10:26918800-26919272	NONHSAT011843
15	lnc-APBB1IP-3	chr10:26921785-26921901	NONHSAT011843
16	lnc-PDSS1-1	chr10:26937880-26937946	NONHSAT011834
17	lnc-ABI1-8	chr10:26906611-26906782	NONHSAT011842
18	lnc-ABI1-1	chr10:26957336-26957423	ENSG00000227932.1
19	lnc-ABI1-1	chr10:26965045-26965088	ENSG00000227932.1
20	lnc-PDSS1-1	chr10:26937187-26937211	NONHSAT011834
21	lnc-APBB1IP-3	chr10:26922869-26923259	NONHSAT011843
22	lnc-ABI1-8	chr10:26908129-26908242	NONHSAT011842
23	lnc-ABI1-8	chr10:26907771-26908030	NONHSAT011841

No data

Variant related genes	Relation type
ENSG00000234296	TF binding region
ENSG00000227932	TF binding region
LINC00202-2	TF binding region
ENSG00000234296	CpG island
ENSG00000227932	CpG island
LINC00202-2	CpG island
ENSG00000227932	chromatin interactions
ENSG00000148459	chromatin interactions
PDGFRA	miRNA target sites
DNMT1	miRNA target sites

Extended variants
information (count: 3371 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:3371 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs787025	chr10:26896432-26896433	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555880900	chr10:26896446-26896447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547620007	chr10:26896458-26896459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576096543	chr10:26896467-26896468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114760627	chr10:26896471-26896472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377212784	chr10:26896490-26896491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561554492	chr10:26896502-26896503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530200246	chr10:26896525-26896526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540955943	chr10:26896529-26896530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184476672	chr10:26896535-26896536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532600799	chr10:26896576-26896577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368961233	chr10:26896579-26896580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs552597963	chr10:26896619-26896620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569236281	chr10:26896657-26896658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188533260	chr10:26896696-26896697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554388410	chr10:26896726-26896727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548357130	chr10:26896737-26896738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192537926	chr10:26896758-26896759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533722824	chr10:26896786-26896787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112842068	chr10:26896834-26896835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117490515	chr10:26896854-26896855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184926842	chr10:26896876-26896877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555742088	chr10:26896878-26896879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575917622	chr10:26896893-26896894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541925332	chr10:26896940-26896941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144647786	chr10:26896949-26896950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189040755	chr10:26896962-26896963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574369967	chr10:26897035-26897036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540828805	chr10:26897037-26897038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560810524	chr10:26897094-26897095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374378676	chr10:26897103-26897104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532866916	chr10:26897117-26897118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546474628	chr10:26897136-26897137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs787024	chr10:26897170-26897171	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs180995298	chr10:26897202-26897203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548688361	chr10:26897221-26897222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568455490	chr10:26897222-26897223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148481314	chr10:26897251-26897252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11015191	chr10:26897279-26897280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570263815	chr10:26897328-26897329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144099222	chr10:26897331-26897332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556473185	chr10:26897350-26897351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574816352	chr10:26897353-26897354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186376359	chr10:26897394-26897395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12260049	chr10:26897395-26897396	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs546234514	chr10:26897397-26897398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555485275	chr10:26897415-26897416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4749170	chr10:26897456-26897457	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534667399	chr10:26897484-26897485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554412010	chr10:26897486-26897487	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26894200-26897600	Enhancers	Fetal Thymus	thymus
2	chr10:26895600-26897000	Enhancers	Thymus	Thymus
3	chr10:26900000-26900200	Enhancers	Stomach Mucosa	stomach
4	chr10:26900200-26900800	Weak transcription	Stomach Mucosa	stomach
5	chr10:26900800-26901200	Enhancers	Duodenum Mucosa	Duodenum
6	chr10:26900800-26901800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr10:26900800-26902200	Enhancers	Liver	Liver
8	chr10:26900800-26902200	Enhancers	Fetal Intestine Small	intestine
9	chr10:26900800-26902200	Enhancers	Stomach Mucosa	stomach
10	chr10:26901200-26901800	Active TSS	Duodenum Mucosa	Duodenum
11	chr10:26901400-26902000	Enhancers	Fetal Intestine Large	intestine
12	chr10:26901800-26902000	Flanking Active TSS	Duodenum Mucosa	Duodenum
13	chr10:26901800-26902200	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr10:26902200-26905600	Weak transcription	Liver	Liver
15	chr10:26902200-26909400	Weak transcription	Stomach Mucosa	stomach
16	chr10:26905600-26906000	Enhancers	Liver	Liver
17	chr10:26905800-26906000	Enhancers	Fetal Thymus	thymus
18	chr10:26906000-26907000	Weak transcription	Fetal Thymus	thymus
19	chr10:26906000-26910800	Weak transcription	Liver	Liver
20	chr10:26907000-26907400	Enhancers	Fetal Thymus	thymus
21	chr10:26907400-26910800	Weak transcription	Fetal Thymus	thymus
22	chr10:26908000-26911200	Weak transcription	Right Atrium	heart
23	chr10:26908400-26908600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr10:26909400-26909800	Enhancers	Stomach Mucosa	stomach
25	chr10:26909400-26910800	Enhancers	Fetal Intestine Small	intestine
26	chr10:26909800-26910000	Enhancers	Fetal Intestine Large	intestine
27	chr10:26909800-26910800	Weak transcription	Stomach Mucosa	stomach
28	chr10:26909800-26911000	Enhancers	Duodenum Mucosa	Duodenum
29	chr10:26910000-26910600	Weak transcription	Fetal Intestine Large	intestine
30	chr10:26910600-26910800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr10:26910600-26910800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr10:26910600-26910800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr10:26910600-26910800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr10:26910600-26910800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr10:26910600-26910800	Enhancers	Fetal Intestine Large	intestine
36	chr10:26910600-26910800	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr10:26910600-26910800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr10:26910600-26910800	Enhancers	NHEK	skin
39	chr10:26910600-26911000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:26910600-26911200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr10:26910600-26911800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr10:26910800-26911000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr10:26910800-26911000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr10:26910800-26911000	Enhancers	Primary hematopoietic stem cells	blood
45	chr10:26910800-26911000	Enhancers	Adipose Nuclei	Adipose
46	chr10:26910800-26911000	Flanking Active TSS	Fetal Intestine Large	intestine
47	chr10:26910800-26911000	Flanking Active TSS	Fetal Intestine Small	intestine
48	chr10:26910800-26911000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
49	chr10:26910800-26911000	Flanking Active TSS	Stomach Mucosa	stomach
50	chr10:26910800-26911000	Enhancers	HMEC	breast

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