Variant report

Variant	nsv550232
Chromosome Location	chr10:26899800-26950603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:430)
CpG islands
(count:919)
Chromatin interactive
region (count:7)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:26917389-26917782	GM12878	blood:	n/a	n/a
2	ATF2	chr10:26917400-26917850	GM12878	blood:	n/a	n/a
3	ATF3	chr10:26926570-26926744	K562	blood:	n/a	chr10:26926582-26926591
4	BACH1	chr10:26910868-26911617	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr10:26911106-26911298	GM12878	blood:	n/a	chr10:26911109-26911117
6	BATF	chr10:26917429-26917718	GM12878	blood:	n/a	n/a
7	BATF	chr10:26917280-26917726	GM12878	blood:	n/a	n/a
8	BATF	chr10:26911081-26911366	GM12878	blood:	n/a	chr10:26911109-26911117
9	BCL11A	chr10:26917343-26917726	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:26926497-26926757	K562	blood:	n/a	n/a
11	BHLHE40	chr10:26917448-26917722	GM12878	blood:	n/a	n/a
12	CEBPB	chr10:26946921-26947139	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:26946966-26947172	K562	blood:	n/a	n/a
14	CEBPB	chr10:26925018-26925342	K562	blood:	n/a	n/a
15	CEBPB	chr10:26910882-26911209	A549	lung:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
16	CEBPB	chr10:26925020-26925337	A549	lung:	n/a	n/a
17	CEBPB	chr10:26910907-26911238	K562	blood:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
18	CEBPB	chr10:26910930-26911239	HepG2	liver:	n/a	chr10:26911053-26911064 chr10:26910983-26910994
19	CEBPB	chr10:26925026-26925341	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:26925024-26925342	IMR90	lung:	n/a	n/a
21	CHD1	chr10:26911280-26911380	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr10:26936600-26936750	GM12878	blood:	n/a	n/a
23	CTCF	chr10:26916320-26916470	GM12872	blood:	n/a	n/a
24	CTCF	chr10:26916291-26916589	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr10:26916467-26916496	GM19238	blood:	n/a	n/a
26	CTCF	chr10:26926839-26926880	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:26916400-26916550	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr10:26916345-26916538	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr10:26916360-26916510	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr10:26936640-26936790	NHEK	skin:	n/a	n/a
31	CTCF	chr10:26916411-26916452	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr10:26936660-26936810	GM12869	blood:	n/a	n/a
33	CTCF	chr10:26905035-26905100	GM20000	blood:	n/a	n/a
34	CTCF	chr10:26950056-26950117	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr10:26916360-26916510	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr10:26934700-26934950	GM12874	blood:	n/a	n/a
37	CTCF	chr10:26916450-26916505	GM19240	blood:	n/a	n/a
38	CTCF	chr10:26916380-26916530	BE2_C	brain:	n/a	n/a
39	CTCF	chr10:26946458-26946503	LNCaP	prostate:	n/a	n/a
40	CTCF	chr10:26936680-26936830	GM12865	blood:	n/a	n/a
41	CTCF	chr10:26934620-26934770	GM12874	blood:	n/a	n/a
42	CTCF	chr10:26936656-26936835	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:26936634-26936875	GM12891	blood:	n/a	n/a
44	CTCF	chr10:26916420-26916570	HAc	cerebellar:	n/a	n/a
45	CTCF	chr10:26916280-26916430	HVMF	connective:	n/a	n/a
46	CTCF	chr10:26936660-26936859	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr10:26916340-26916490	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr10:26936680-26936830	SAEC	small airway:	n/a	n/a
49	CTCF	chr10:26936660-26936810	GM12866	blood:	n/a	n/a
50	CTCF	chr10:26936652-26936841	GM12878	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	chr10:26931986-26932036	Hela-S3	cervix:	n/a
2	chr10:26942225-26942275	HCPEpiC	choroid plexus:	n/a
3	chr10:26931912-26931962	HAEpiC	amniotic membrane:	n/a
4	chr10:26931731-26931781	Caco-2	colon:	n/a
5	chr10:26931986-26932036	Hela-S3	cervix:	n/a
6	chr10:26942225-26942275	HCPEpiC	choroid plexus:	n/a
7	chr10:26931912-26931962	HAEpiC	amniotic membrane:	n/a
8	chr10:26931731-26931781	Caco-2	colon:	n/a
9	chr10:26931731-26931781	AoSMC	blood vessel:	n/a
10	chr10:26931991-26932041	HIPEpiC	eye:	n/a
11	chr10:26931794-26931844	HIPEpiC	eye:	n/a
12	chr10:26931991-26932041	HAEpiC	amniotic membrane:	n/a
13	chr10:26942165-26942215	HepG2	liver:	n/a
14	chr10:26931986-26932036	K562	blood:	n/a
15	chr10:26930863-26930913	Hela-S3	cervix:	n/a
16	chr10:26931969-26932019	NT2-D1	testis:	n/a
17	chr10:26931731-26931781	SKMC	muscle:	n/a
18	chr10:26942165-26942215	HMEC	breast:	n/a
19	chr10:26942165-26942215	RPTEC	kidney:	n/a
20	chr10:26931926-26931976	HCF	heart:	n/a
21	chr10:26942225-26942275	RPTEC	kidney:	n/a
22	chr10:26911451-26911501	BJ	skin:	n/a
23	chr10:26932057-26932107	GM12892	blood:	n/a
24	chr10:26932036-26932086	AoSMC	blood vessel:	n/a
25	chr10:26931978-26932028	NH-A	brain:	n/a
26	chr10:26942225-26942275	SKMC	muscle:	n/a
27	chr10:26932036-26932086	NHBE	bronchial:	n/a
28	chr10:26931978-26932028	IMR90	lung:	fetal
29	chr10:26931991-26932041	HEK293	kidney:	embryo
30	chr10:26942225-26942275	BJ	skin:	n/a
31	chr10:26931978-26932028	SKMC	muscle:	n/a
32	chr10:26932036-26932086	HL-60	blood:	n/a
33	chr10:26931731-26931781	GM12878	blood:	n/a
34	chr10:26911186-26911236	HMEC	breast:	n/a
35	chr10:26932036-26932086	HAEpiC	amniotic membrane:	n/a
36	chr10:26931991-26932041	HCPEpiC	choroid plexus:	n/a
37	chr10:26931912-26931962	HMEC	breast:	n/a
38	chr10:26932036-26932086	CMK	blood:	n/a
39	chr10:26931912-26931962	SAEC	small airway:	n/a
40	chr10:26931986-26932036	Hepatocyte	liver:	n/a
41	chr10:26931926-26931976	ECC-1	luminal epithelium:	n/a
42	chr10:26911451-26911501	GM19239	blood:	n/a
43	chr10:26942225-26942275	AG09309	skin:	n/a
44	chr10:26932057-26932107	MCF-7	breast:	n/a
45	chr10:26931794-26931844	NH-A	brain:	n/a
46	chr10:26931912-26931962	PANC-1	pancreas:	n/a
47	chr10:26931991-26932041	Hela-S3	cervix:	n/a
48	chr10:26931912-26931962	SK-N-SH_RA	brain:	n/a
49	chr10:26931926-26931976	HCPEpiC	choroid plexus:	n/a
50	chr10:26932036-26932086	K562	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
2	chr10:26942956..26944932-chr10:26949482..26951411,2	K562	blood:
3	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
4	chr10:26948657..26951534-chr10:26954538..26957242,4	K562	blood:
5	chr10:26942956..26945018-chr10:26949482..26951597,3	K562	blood:
6	chr10:26944728..26946269-chr10:26952549..26954691,2	K562	blood:
7	chr10:26911042..26911570-chr17:41400814..41401666,2	NB4	blood:

(count:20 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 2510 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:2510 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562220166	chr10:26900013-26900014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183246370	chr10:26900021-26900022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560680961	chr10:26900032-26900033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111948070	chr10:26900059-26900060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546263558	chr10:26900073-26900074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188216540	chr10:26900176-26900177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528648749	chr10:26900184-26900185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143359128	chr10:26900196-26900197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7074426	chr10:26900228-26900229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537304243	chr10:26900231-26900232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193171532	chr10:26900240-26900241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550952692	chr10:26900260-26900261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567521859	chr10:26900286-26900287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144753735	chr10:26900288-26900289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552812442	chr10:26900316-26900317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10829034	chr10:26900319-26900320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs538831806	chr10:26900334-26900335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559838547	chr10:26900339-26900340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184641983	chr10:26900346-26900347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565815139	chr10:26900356-26900357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544132088	chr10:26900357-26900358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188384326	chr10:26900387-26900388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372427768	chr10:26900401-26900402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539974369	chr10:26900404-26900405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191375263	chr10:26900419-26900420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74521607	chr10:26900483-26900484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545203933	chr10:26900517-26900518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151025268	chr10:26900540-26900541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531254610	chr10:26900545-26900546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550957243	chr10:26900546-26900547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142650663	chr10:26900547-26900548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530093545	chr10:26900575-26900576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11015194	chr10:26900583-26900584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs147953512	chr10:26900584-26900585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12774408	chr10:26900595-26900596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183952537	chr10:26900677-26900678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558720648	chr10:26900680-26900681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188286777	chr10:26900777-26900778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569622586	chr10:26900799-26900800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538161030	chr10:26900809-26900810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79205149	chr10:26900816-26900817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554555392	chr10:26900913-26900914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574125327	chr10:26900935-26900936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539841743	chr10:26900945-26900946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116038373	chr10:26900961-26900962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73594382	chr10:26900973-26900974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77924567	chr10:26900991-26900992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs56113330	chr10:26900998-26900999	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs530995775	chr10:26901000-26901001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544916084	chr10:26901049-26901050	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:42)

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
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

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

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