Variant report

Variant	esv2753357
Chromosome Location	chr13:92903199-93026399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:517)
CpG islands
(count:0)
Chromatin interactive
region (count:55)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:93007422-93007801	K562	blood:	n/a	n/a
2	ARID3A	chr13:92946163-92946351	K562	blood:	n/a	n/a
3	ATF1	chr13:92991024-92991295	K562	blood:	n/a	n/a
4	ATF1	chr13:92989785-92989940	K562	blood:	n/a	n/a
5	ATF1	chr13:92985734-92986088	K562	blood:	n/a	n/a
6	ATF1	chr13:93018071-93018476	K562	blood:	n/a	n/a
7	ATF1	chr13:93000542-93000602	K562	blood:	n/a	n/a
8	ATF1	chr13:92969411-92969828	K562	blood:	n/a	n/a
9	ATF1	chr13:92977355-92978161	K562	blood:	n/a	n/a
10	ATF1	chr13:92971259-92971965	K562	blood:	n/a	n/a
11	ATF1	chr13:92973596-92973794	K562	blood:	n/a	n/a
12	ATF1	chr13:92960313-92960935	K562	blood:	n/a	n/a
13	ATF1	chr13:92988289-92989010	K562	blood:	n/a	n/a
14	ATF1	chr13:93008905-93009443	K562	blood:	n/a	n/a
15	ATF1	chr13:92948124-92948617	K562	blood:	n/a	n/a
16	ATF1	chr13:93023686-93024321	K562	blood:	n/a	n/a
17	ATF1	chr13:92976143-92976957	K562	blood:	n/a	n/a
18	ATF1	chr13:92989310-92989318	K562	blood:	n/a	n/a
19	BACH1	chr13:92998581-92998621	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr13:92957878-92958229	K562	blood:	n/a	n/a
21	BACH1	chr13:92918602-92918948	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr13:93011566-93011568	K562	blood:	n/a	n/a
23	BATF	chr13:92967550-92967856	GM12878	blood:	n/a	chr13:92967690-92967701
24	BATF	chr13:92967590-92967851	GM12878	blood:	n/a	chr13:92967690-92967701
25	BCL11A	chr13:92967565-92967763	GM12878	blood:	n/a	n/a
26	BHLHE40	chr13:92950981-92951037	K562	blood:	n/a	n/a
27	BHLHE40	chr13:93007542-93007875	K562	blood:	n/a	n/a
28	CCNT2	chr13:92976086-92976237	K562	blood:	n/a	n/a
29	CCNT2	chr13:92960086-92960453	K562	blood:	n/a	n/a
30	CCNT2	chr13:93018008-93018434	K562	blood:	n/a	n/a
31	CCNT2	chr13:92991177-92991375	K562	blood:	n/a	n/a
32	CEBPB	chr13:92950970-92951099	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr13:92955817-92956017	A549	lung:	n/a	chr13:92955901-92955912
34	CEBPB	chr13:92914787-92915067	IMR90	lung:	n/a	n/a
35	CEBPB	chr13:92918042-92918158	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr13:92927467-92927683	HepG2	liver:	n/a	chr13:92927519-92927536 chr13:92927520-92927533 chr13:92927602-92927613
37	CEBPB	chr13:92914870-92915053	A549	lung:	n/a	n/a
38	CEBPB	chr13:92929341-92929351	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr13:92970428-92970745	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr13:92965732-92965919	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr13:92917082-92917132	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr13:92955774-92956106	K562	blood:	n/a	chr13:92955901-92955912
43	CEBPB	chr13:92927550-92927683	A549	lung:	n/a	chr13:92927602-92927613
44	CEBPB	chr13:92955779-92956034	IMR90	lung:	n/a	chr13:92955901-92955912
45	CEBPB	chr13:92960630-92960977	K562	blood:	n/a	chr13:92960815-92960826
46	CEBPB	chr13:92955819-92956028	HepG2	liver:	n/a	chr13:92955901-92955912
47	CEBPB	chr13:92942320-92942641	HepG2	liver:	n/a	chr13:92942469-92942480 chr13:92942468-92942479 chr13:92942468-92942481 chr13:92942468-92942481
48	CEBPB	chr13:92942315-92942623	IMR90	lung:	n/a	chr13:92942469-92942480 chr13:92942468-92942479 chr13:92942468-92942481 chr13:92942468-92942481
49	CHD2	chr13:92950384-92950494	K562	blood:	n/a	n/a
50	CHD2	chr13:93020251-93020278	K562	blood:	n/a	n/a

No data

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:92962787..92965087-chr13:92966991..92969071,2	K562	blood:
2	chr13:92010706..92013622-chr13:93006752..93008493,2	K562	blood:
3	chr13:93012828..93015636-chr13:93017565..93019548,2	K562	blood:
4	chr13:92961385..92963031-chr13:92979111..92982076,2	K562	blood:
5	chr13:92964628..92966987-chr13:92977426..92979496,2	K562	blood:
6	chr13:92980924..92984645-chr13:92987086..92990340,3	K562	blood:
7	chr13:92995861..92998163-chr13:93022468..93024947,2	K562	blood:
8	chr13:92010436..92012496-chr13:92953050..92954701,2	K562	blood:
9	chr13:92962787..92965087-chr13:92966991..92969071,2	K562	blood:
10	chr13:92965451..92968338-chr13:92972669..92975627,2	K562	blood:
11	chr13:92968259..92969910-chr13:92996026..92998901,2	K562	blood:
12	chr13:92965487..92967711-chr13:92976361..92978926,2	K562	blood:
13	chr13:93024437..93027101-chr13:93028065..93030296,2	K562	blood:
14	chr13:93013213..93015773-chr13:93023566..93027348,3	K562	blood:
15	chr13:92968259..92969910-chr13:92996026..92998901,2	K562	blood:
16	chr13:92995861..92998163-chr13:93022468..93024947,2	K562	blood:
17	chr13:92986047..92988836-chr13:93080866..93083328,2	K562	blood:
18	chr13:92987424..92989331-chr13:92989713..92992513,2	K562	blood:
19	chr13:92982264..92985131-chr13:93004741..93006675,2	K562	blood:
20	chr13:92839355..92840221-chr13:93007230..93007787,2	MCF-7	breast:
21	chr13:93013213..93015773-chr13:93023566..93027348,3	K562	blood:
22	chr13:92956827..92958387-chr13:92959759..92961351,2	K562	blood:
23	chr13:92965487..92967711-chr13:92976361..92978926,2	K562	blood:
24	chr13:92980924..92984645-chr13:92987086..92990340,3	K562	blood:
25	chr13:92961385..92963031-chr13:92979111..92982076,2	K562	blood:
26	chr13:92983817..92985368-chr13:93015068..93017856,2	K562	blood:
27	chr13:92958679..92961533-chr13:93089880..93091566,2	K562	blood:
28	chr13:93018970..93021048-chr13:93021164..93022779,2	K562	blood:
29	chr13:92982264..92985131-chr13:93004741..93006675,2	K562	blood:
30	chr13:92985419..92987954-chr13:93220833..93223543,2	K562	blood:
31	chr13:92981004..92983533-chr13:93023966..93025848,2	K562	blood:
32	chr13:92951893..92954281-chr13:92957574..92960507,2	K562	blood:
33	chr13:93026262..93028061-chr13:93041707..93043886,2	K562	blood:
34	chr13:92970236..92973225-chr13:92975344..92980353,5	K562	blood:
35	chr13:92951893..92954281-chr13:92957574..92960507,2	K562	blood:
36	chr13:92965451..92968338-chr13:92972669..92975627,2	K562	blood:
37	chr13:92987424..92989331-chr13:92989713..92992513,2	K562	blood:
38	chr13:92964628..92966987-chr13:92977426..92979496,2	K562	blood:
39	chr13:92957496..92960008-chr13:92963128..92965362,2	K562	blood:
40	chr13:92984785..92987410-chr13:92992278..92995322,3	K562	blood:
41	chr13:92970236..92973225-chr13:92975344..92980353,5	K562	blood:
42	chr13:93004690..93006667-chr13:93012295..93015000,2	K562	blood:
43	chr13:93024752..93026535-chr13:93034305..93036660,2	K562	blood:
44	chr13:92957176..92958871-chr13:92997001..92998891,2	K562	blood:
45	chr13:92983817..92985368-chr13:93015068..93017856,2	K562	blood:
46	chr13:92957496..92960008-chr13:92963128..92965362,2	K562	blood:
47	chr13:92983145..92985904-chr13:92987086..92990641,3	K562	blood:
48	chr13:92981004..92983533-chr13:93023966..93025848,2	K562	blood:
49	chr13:92841987..92842813-chr13:93007626..93008163,2	MCF-7	breast:
50	chr13:93012828..93015636-chr13:93017565..93019548,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCT-5	chr13:92992650-92992856	ENSG00000232885.1
2	lnc-DCT-5	chr13:92992047-92992240	ENSG00000232885.1

No data

Variant related genes	Relation type
GPC5-AS2	TF binding region
ENSG00000232885	chromatin interactions

Extended variants
information (count: 2289 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2289 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115836258	chr13:92903266-92903267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75011160	chr13:92903272-92903273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577416499	chr13:92903308-92903309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377427778	chr13:92903312-92903313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555535891	chr13:92903318-92903319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572540630	chr13:92903336-92903337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541062342	chr13:92903337-92903338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1926616	chr13:92903339-92903340	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs533190686	chr13:92903360-92903361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544102966	chr13:92903426-92903427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563976462	chr13:92903429-92903430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs56183342	chr13:92903450-92903451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529470043	chr13:92903475-92903476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555851376	chr13:92903487-92903488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150755373	chr13:92903528-92903529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7338926	chr13:92903538-92903539	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs190052079	chr13:92903588-92903589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79239577	chr13:92903625-92903626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs8002066	chr13:92903671-92903672	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs115979617	chr13:92903680-92903681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555991369	chr13:92903683-92903684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374391793	chr13:92903720-92903721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569621531	chr13:92903733-92903734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535258686	chr13:92903796-92903797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181294632	chr13:92903862-92903863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373112549	chr13:92903926-92903927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185859574	chr13:92903938-92903939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139088536	chr13:92903944-92903945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192050868	chr13:92903987-92903988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144002167	chr13:92903992-92903993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566977514	chr13:92904008-92904009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183477078	chr13:92904070-92904071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529660397	chr13:92904076-92904077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543222534	chr13:92904103-92904104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370459902	chr13:92904121-92904122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188942003	chr13:92904216-92904217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559930647	chr13:92904217-92904218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528694315	chr13:92904230-92904231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9560997	chr13:92904269-92904270	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs114564983	chr13:92904288-92904289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532724531	chr13:92904301-92904302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563256956	chr13:92904311-92904312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117548613	chr13:92904384-92904385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377344311	chr13:92904548-92904549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11841338	chr13:92904552-92904553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115427789	chr13:92904575-92904576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192012770	chr13:92904582-92904583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565843338	chr13:92904593-92904594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74107158	chr13:92904636-92904637	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182234503	chr13:92904637-92904638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92902600-92904400	Enhancers	Fetal Lung	lung
2	chr13:92902800-92907000	Weak transcription	Fetal Stomach	stomach
3	chr13:92904000-92904400	Enhancers	Fetal Kidney	kidney
4	chr13:92904400-92906800	Weak transcription	Fetal Lung	lung
5	chr13:92906800-92907800	Enhancers	Fetal Lung	lung
6	chr13:92907000-92907600	Enhancers	Fetal Stomach	stomach
7	chr13:92907800-92911800	Weak transcription	Fetal Lung	lung
8	chr13:92908000-92909600	Enhancers	Adipose Nuclei	Adipose
9	chr13:92911800-92912000	Enhancers	Fetal Lung	lung
10	chr13:92912000-92912400	Weak transcription	Fetal Lung	lung
11	chr13:92912000-92912400	Enhancers	Ovary	ovary
12	chr13:92912000-92912800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr13:92912400-92913200	Enhancers	Fetal Lung	lung
14	chr13:92912800-92917600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr13:92914200-92915000	Enhancers	Colon Smooth Muscle	Colon
16	chr13:92917200-92918200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr13:92917600-92919000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr13:92917600-92919000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:92918000-92919000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr13:92918800-92919000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr13:92922400-92922800	Enhancers	Rectal Smooth Muscle	rectum
22	chr13:92933000-92933800	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr13:92933200-92933400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr13:92933200-92933800	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr13:92943400-92943600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr13:92943600-92950400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr13:92950400-92950600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr13:92950800-92951000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr13:92950800-92951000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr13:92950800-92951200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr13:92950800-92951600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr13:92951000-92951600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr13:92951000-92952600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr13:92951200-92952400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr13:92951600-92951800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr13:92952400-92952800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr13:92952400-92953800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr13:92953200-92953600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:92954400-92956200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr13:92955600-92956200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr13:92958600-92959000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr13:92958600-92959000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr13:92958600-92959000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr13:92958800-92959200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr13:92960000-92960600	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr13:92965800-92966000	Enhancers	Ovary	ovary
47	chr13:92965800-92966200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr13:92966400-92966600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:92966600-92967600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr13:92967000-92967400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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