Variant report

Variant	nsv894930
Chromosome Location	chr10:19696007-19793195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:19792017-19792188	K562	blood:	n/a	n/a
2	BACH1	chr10:19777970-19778068	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr10:19695758-19696077	K562	blood:	n/a	n/a
4	CEBPB	chr10:19758531-19758806	IMR90	lung:	n/a	chr10:19758672-19758683
5	CEBPB	chr10:19789951-19790296	MCF-7	breast:	n/a	n/a
6	CEBPB	chr10:19787872-19788258	MCF-7	breast:	n/a	chr10:19788093-19788106 chr10:19788094-19788105 chr10:19788093-19788106 chr10:19788093-19788104 chr10:19788093-19788106
7	CEBPB	chr10:19721069-19721224	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr10:19781986-19782089	K562	blood:	n/a	n/a
9	CEBPB	chr10:19710815-19710994	K562	blood:	n/a	chr10:19710892-19710903
10	CEBPB	chr10:19737802-19737993	HepG2	liver:	n/a	chr10:19737941-19737954 chr10:19737943-19737952 chr10:19737943-19737954
11	CEBPB	chr10:19703654-19703971	HepG2	liver:	n/a	chr10:19703745-19703758 chr10:19703799-19703810 chr10:19703801-19703810 chr10:19703800-19703811 chr10:19703747-19703758 chr10:19703747-19703758
12	CEBPB	chr10:19703713-19703880	A549	lung:	n/a	chr10:19703745-19703758 chr10:19703799-19703810 chr10:19703801-19703810 chr10:19703800-19703811 chr10:19703747-19703758 chr10:19703747-19703758
13	CEBPB	chr10:19787873-19788271	MCF-7	breast:	n/a	chr10:19788093-19788106 chr10:19788094-19788105 chr10:19788093-19788106 chr10:19788093-19788104 chr10:19788093-19788106
14	CEBPB	chr10:19770776-19771101	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:19710723-19711033	HepG2	liver:	n/a	chr10:19710892-19710903
16	CEBPB	chr10:19721715-19722074	HepG2	liver:	n/a	chr10:19721890-19721907 chr10:19721888-19721905
17	CEBPB	chr10:19721890-19721917	H1-hESC	embryonic stem cell:	n/a	chr10:19721890-19721907
18	CEBPB	chr10:19758519-19758826	HepG2	liver:	n/a	chr10:19758672-19758683
19	CEBPB	chr10:19710721-19710987	H1-hESC	embryonic stem cell:	n/a	chr10:19710892-19710903
20	CEBPB	chr10:19703706-19703978	IMR90	lung:	n/a	chr10:19703745-19703758 chr10:19703799-19703810 chr10:19703801-19703810 chr10:19703800-19703811 chr10:19703747-19703758 chr10:19703747-19703758
21	CEBPB	chr10:19787938-19788228	IMR90	lung:	n/a	chr10:19788093-19788106 chr10:19788094-19788105 chr10:19788093-19788106 chr10:19788093-19788104 chr10:19788093-19788106
22	CEBPB	chr10:19781460-19782153	HepG2	liver:	n/a	chr10:19781628-19781639
23	CEBPB	chr10:19787923-19788214	A549	lung:	n/a	chr10:19788093-19788106 chr10:19788094-19788105 chr10:19788093-19788106 chr10:19788093-19788104 chr10:19788093-19788106
24	CEBPB	chr10:19721009-19721343	HepG2	liver:	n/a	chr10:19721276-19721289 chr10:19721289-19721302 chr10:19721289-19721300 chr10:19721254-19721267 chr10:19721289-19721302
25	CEBPB	chr10:19721050-19721310	IMR90	lung:	n/a	chr10:19721276-19721289 chr10:19721289-19721302 chr10:19721289-19721300 chr10:19721254-19721267 chr10:19721289-19721302
26	CEBPB	chr10:19710725-19711045	IMR90	lung:	n/a	chr10:19710892-19710903
27	CEBPB	chr10:19781492-19782070	IMR90	lung:	n/a	chr10:19781628-19781639
28	CEBPB	chr10:19737930-19737982	K562	blood:	n/a	chr10:19737941-19737954 chr10:19737943-19737952 chr10:19737943-19737954
29	CEBPB	chr10:19787930-19788238	HepG2	liver:	n/a	chr10:19788093-19788106 chr10:19788094-19788105 chr10:19788093-19788106 chr10:19788093-19788104 chr10:19788093-19788106
30	CEBPB	chr10:19721727-19722058	IMR90	lung:	n/a	chr10:19721890-19721907 chr10:19721888-19721905
31	CEBPB	chr10:19721794-19722030	A549	lung:	n/a	chr10:19721890-19721907 chr10:19721888-19721905
32	CHD2	chr10:19777819-19778173	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr10:19777820-19777970	AG09319	gingival:	n/a	n/a
34	CTCF	chr10:19700180-19700334	MCF-7	breast:	n/a	chr10:19700245-19700258
35	CTCF	chr10:19700180-19700330	HBMEC	blood vessel:	n/a	chr10:19700245-19700258
36	CTCF	chr10:19701600-19701750	GM12872	blood:	n/a	chr10:19701642-19701655 chr10:19701639-19701657 chr10:19701641-19701662 chr10:19701642-19701651 chr10:19701644-19701654
37	CTCF	chr10:19754051-19754081	GM10266	blood:	n/a	n/a
38	CTCF	chr10:19783020-19783170	GM12872	blood:	n/a	n/a
39	CTCF	chr10:19700240-19700390	AG04450	lung:	n/a	chr10:19700245-19700258
40	CTCF	chr10:19700220-19700370	NHEK	skin:	n/a	chr10:19700245-19700258
41	CTCF	chr10:19701540-19701690	HUVEC	blood vessel:	n/a	chr10:19701642-19701655 chr10:19701639-19701657 chr10:19701641-19701662 chr10:19701642-19701651 chr10:19701644-19701654
42	CTCF	chr10:19700180-19700330	HCPEpiC	choroid plexus:	n/a	chr10:19700245-19700258
43	CTCF	chr10:19777860-19778010	HMF	breast:	n/a	n/a
44	CTCF	chr10:19701540-19701690	HEEpiC	esophagus:	n/a	chr10:19701642-19701655 chr10:19701639-19701657 chr10:19701641-19701662 chr10:19701642-19701651 chr10:19701644-19701654
45	CTCF	chr10:19701561-19701751	NHEK	skin:	n/a	chr10:19701642-19701655 chr10:19701639-19701657 chr10:19701641-19701662 chr10:19701642-19701651 chr10:19701644-19701654
46	CTCF	chr10:19700120-19700270	HFF	foreskin:	n/a	chr10:19700245-19700258
47	CTCF	chr10:19701532-19701699	SK-N-SH_RA	brain:	n/a	chr10:19701642-19701655 chr10:19701639-19701657 chr10:19701641-19701662 chr10:19701642-19701651 chr10:19701644-19701654
48	CTCF	chr10:19777924-19777992	GM12892	blood:	n/a	n/a
49	CTCF	chr10:19701580-19701730	BJ	skin:	n/a	chr10:19701642-19701655 chr10:19701639-19701657 chr10:19701641-19701662 chr10:19701642-19701651 chr10:19701644-19701654
50	CTCF	chr10:19701180-19701330	HRPEpiC	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:19705290-19705340	HEEpiC	esophagus:	n/a
2	chr10:19778008-19778058	MCF-7	breast:	n/a
3	chr10:19705290-19705340	NH-A	brain:	n/a
4	chr10:19705290-19705340	AoSMC	blood vessel:	n/a
5	chr10:19778008-19778058	PrEC	prostate:	n/a
6	chr10:19705290-19705340	HUVEC	blood vessel:	n/a
7	chr10:19778008-19778058	HCPEpiC	choroid plexus:	n/a
8	chr10:19778008-19778058	GM06990	blood:	n/a
9	chr10:19705290-19705340	NT2-D1	testis:	n/a
10	chr10:19705290-19705340	U87	brain:	n/a
11	chr10:19778008-19778058	AoSMC	blood vessel:	n/a
12	chr10:19705290-19705340	HL-60	blood:	n/a
13	chr10:19705290-19705340	K562	blood:	n/a
14	chr10:19778008-19778058	HepG2	liver:	n/a
15	chr10:19705290-19705340	SK-N-SH	brain:	n/a
16	chr10:19705290-19705340	HAEpiC	amniotic membrane:	n/a
17	chr10:19778008-19778058	AG04450	lung:	fetal
18	chr10:19705290-19705340	ovcar-3	ovarian:	n/a
19	chr10:19705290-19705340	Jurkat	blood:	n/a
20	chr10:19778008-19778058	ECC-1	luminal epithelium:	n/a
21	chr10:19778008-19778058	RPTEC	kidney:	n/a
22	chr10:19705290-19705340	T-47D	breast:	n/a
23	chr10:19778008-19778058	HIPEpiC	eye:	n/a
24	chr10:19778008-19778058	HL-60	blood:	n/a
25	chr10:19705290-19705340	MCF-7	breast:	n/a
26	chr10:19778008-19778058	GM19239	blood:	n/a
27	chr10:19778008-19778058	Jurkat	blood:	n/a
28	chr10:19705290-19705340	MCF10A-Er-Src	breast:	n/a
29	chr10:19778008-19778058	NHDF-neo	bronchial:	n/a
30	chr10:19778008-19778058	NB4	blood:	n/a
31	chr10:19705290-19705340	BE2_C	brain:	n/a
32	chr10:19705290-19705340	LNCaP	prostate:	n/a
33	chr10:19778008-19778058	ovcar-3	ovarian:	n/a
34	chr10:19705290-19705340	Caco-2	colon:	n/a
35	chr10:19705290-19705340	PFSK-1	brain:	n/a
36	chr10:19778008-19778058	NH-A	brain:	n/a
37	chr10:19705290-19705340	GM12891	blood:	n/a
38	chr10:19705290-19705340	HRPEpiC	eye:	n/a
39	chr10:19778008-19778058	AG04449	skin:	fetal
40	chr10:19778008-19778058	NHBE	bronchial:	n/a
41	chr10:19778008-19778058	BJ	skin:	n/a
42	chr10:19705290-19705340	PrEC	prostate:	n/a
43	chr10:19705290-19705340	ProgFib	skin:	n/a
44	chr10:19778008-19778058	A549	lung:	n/a
45	chr10:19705290-19705340	HIPEpiC	eye:	n/a
46	chr10:19705290-19705340	HCT-116	colon:	n/a
47	chr10:19778008-19778058	HMEC	breast:	n/a
48	chr10:19705290-19705340	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:19778008-19778058	HUVEC	blood vessel:	n/a
50	chr10:19778008-19778058	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:19702800..19704977-chr10:19710060..19711569,2	MCF-7	breast:
2	chr10:19785625..19787709-chr10:19788365..19791040,2	MCF-7	breast:
3	chr10:19701583..19703629-chr10:19722720..19725656,2	MCF-7	breast:
4	chr10:19784572..19786146-chr10:19787649..19789922,2	MCF-7	breast:
5	chr10:19701583..19703629-chr10:19722720..19725656,2	MCF-7	breast:
6	chr10:19769588..19771872-chr10:19775105..19777621,2	K562	blood:
7	chr10:19785625..19787709-chr10:19788365..19791040,2	MCF-7	breast:
8	chr10:19781369..19782958-chr10:19786296..19789278,2	MCF-7	breast:
9	chr10:19784572..19786146-chr10:19787649..19789922,2	MCF-7	breast:
10	chr10:19702800..19704977-chr10:19710060..19711569,2	MCF-7	breast:
11	chr10:19781369..19782958-chr10:19786296..19789278,2	MCF-7	breast:
12	chr10:19724105..19725802-chr10:19728835..19730495,2	K562	blood:
13	chr10:19776078..19778713-chr10:19790449..19792992,2	K562	blood:
14	chr10:18978169..18978867-chr10:19699824..19700403,3	MCF-7	breast:
15	chr10:19724105..19725802-chr10:19728835..19730495,2	K562	blood:
16	chr10:19709784..19712687-chr10:19713625..19715285,2	K562	blood:
17	chr10:19709784..19712687-chr10:19713625..19715285,2	K562	blood:
18	chr10:19701065..19702056-chr10:20076746..20077511,2	MCF-7	breast:
19	chr10:19704403..19706854-chr10:20104452..20106050,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NSUN6-7	chr10:19780001-19780228	NONHSAT011662
2	lnc-PLXDC2-6	chr10:19778030-19778329	NONHSAT011661

Variant related genes	Relation type
HMGN1P20	TF binding region
MALRD1	TF binding region
ENSG00000236960	TF binding region
HMGN1P20	CpG island
MALRD1	CpG island
ENSG00000236960	CpG island
ENSG00000120594	chromatin interactions
ENSG00000204740	chromatin interactions
ENSG00000239539	chromatin interactions

Extended variants
information (count: 4524 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:4524 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386741625	chr10:19696007-19696008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs150871383	chr10:19696009-19696010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140116479	chr10:19696086-19696087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115482118	chr10:19696098-19696099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560974511	chr10:19696136-19696137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111903469	chr10:19696149-19696150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79891075	chr10:19696275-19696276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372519323	chr10:19696283-19696284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192243176	chr10:19696301-19696302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12265167	chr10:19696433-19696434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184308017	chr10:19696454-19696455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551391681	chr10:19696490-19696491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73593902	chr10:19696513-19696514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs371985574	chr10:19696552-19696553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531147341	chr10:19696560-19696561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147337781	chr10:19696600-19696601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187191912	chr10:19696642-19696643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536102368	chr10:19696718-19696719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192919164	chr10:19696725-19696726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139407515	chr10:19696741-19696742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59660712	chr10:19696746-19696747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538713706	chr10:19696796-19696797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144931306	chr10:19696808-19696809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575309384	chr10:19696885-19696886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184594949	chr10:19696891-19696892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559677160	chr10:19696930-19696931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554808233	chr10:19696939-19696940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117540432	chr10:19696977-19696978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148644433	chr10:19696979-19696980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564719309	chr10:19696993-19696994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533286729	chr10:19697071-19697072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548399081	chr10:19697076-19697077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189527821	chr10:19697165-19697166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142128874	chr10:19697167-19697168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530885206	chr10:19697180-19697181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549418865	chr10:19697196-19697197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374939891	chr10:19697199-19697200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567912094	chr10:19697238-19697239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528700409	chr10:19697251-19697252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180767635	chr10:19697254-19697255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571853216	chr10:19697289-19697290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538778002	chr10:19697304-19697305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4428968	chr10:19697320-19697321	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs568771460	chr10:19697322-19697323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12771012	chr10:19697332-19697333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12771746	chr10:19697333-19697334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs151191531	chr10:19697335-19697336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140363955	chr10:19697337-19697338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12771757	chr10:19697339-19697340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12771759	chr10:19697341-19697342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
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
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19681000-19728200	Weak transcription	Fetal Intestine Small	intestine
2	chr10:19695400-19739200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr10:19695800-19696200	Strong transcription	Fetal Intestine Large	intestine
4	chr10:19696200-19705200	Weak transcription	Fetal Intestine Large	intestine
5	chr10:19703400-19703600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr10:19703600-19704800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr10:19703600-19705400	Enhancers	Liver	Liver
8	chr10:19704000-19705000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr10:19704600-19705200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr10:19704800-19705200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr10:19704800-19705200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr10:19704800-19705200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr10:19704800-19706200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr10:19704800-19706800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr10:19704800-19707000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr10:19705000-19705200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr10:19705000-19705600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:19705200-19705400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr10:19705200-19705400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr10:19705200-19705600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr10:19705200-19705600	Enhancers	Fetal Intestine Large	intestine
22	chr10:19705200-19705800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr10:19705200-19705800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr10:19705200-19706200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr10:19705400-19705600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr10:19705400-19705800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr10:19705600-19705800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr10:19705600-19706000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr10:19705600-19706000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr10:19705600-19739000	Weak transcription	Fetal Intestine Large	intestine
31	chr10:19705800-19709600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr10:19705800-19709600	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr10:19705800-19709800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr10:19706000-19709000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr10:19706000-19709600	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr10:19706200-19706600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr10:19706200-19708600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr10:19706600-19706800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr10:19706800-19707000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr10:19706800-19707800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr10:19706800-19709400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr10:19707000-19708600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr10:19707800-19708600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr10:19708600-19708800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr10:19708600-19709400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr10:19708600-19711400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr10:19708800-19709200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr10:19708800-19712800	Enhancers	Fetal Lung	lung
49	chr10:19709000-19709200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr10:19709200-19711400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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