Variant report

Variant	nsv1036835
Chromosome Location	chr13:92953101-93039812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:475)
CpG islands
(count:0)
Chromatin interactive
region (count:69)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	ATF1	chr13:92969411-92969828	K562	blood:	n/a	n/a
3	ATF1	chr13:92977355-92978161	K562	blood:	n/a	n/a
4	ATF1	chr13:93008905-93009443	K562	blood:	n/a	n/a
5	ATF1	chr13:92971259-92971965	K562	blood:	n/a	n/a
6	ATF1	chr13:93000542-93000602	K562	blood:	n/a	n/a
7	ATF1	chr13:92973596-92973794	K562	blood:	n/a	n/a
8	ATF1	chr13:93033932-93034002	K562	blood:	n/a	n/a
9	ATF1	chr13:92989785-92989940	K562	blood:	n/a	n/a
10	ATF1	chr13:92985734-92986088	K562	blood:	n/a	n/a
11	ATF1	chr13:92976143-92976957	K562	blood:	n/a	n/a
12	ATF1	chr13:93018071-93018476	K562	blood:	n/a	n/a
13	ATF1	chr13:92989310-92989318	K562	blood:	n/a	n/a
14	ATF1	chr13:92988289-92989010	K562	blood:	n/a	n/a
15	ATF1	chr13:92991024-92991295	K562	blood:	n/a	n/a
16	ATF1	chr13:93023686-93024321	K562	blood:	n/a	n/a
17	ATF1	chr13:92960313-92960935	K562	blood:	n/a	n/a
18	BACH1	chr13:92957878-92958229	K562	blood:	n/a	n/a
19	BACH1	chr13:92998581-92998621	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr13:93011566-93011568	K562	blood:	n/a	n/a
21	BATF	chr13:92967590-92967851	GM12878	blood:	n/a	chr13:92967690-92967701
22	BATF	chr13:92967550-92967856	GM12878	blood:	n/a	chr13:92967690-92967701
23	BCL11A	chr13:92967565-92967763	GM12878	blood:	n/a	n/a
24	BHLHE40	chr13:93007542-93007875	K562	blood:	n/a	n/a
25	BHLHE40	chr13:93032155-93032279	K562	blood:	n/a	n/a
26	CCNT2	chr13:92991177-92991375	K562	blood:	n/a	n/a
27	CCNT2	chr13:93018008-93018434	K562	blood:	n/a	n/a
28	CCNT2	chr13:92960086-92960453	K562	blood:	n/a	n/a
29	CCNT2	chr13:92976086-92976237	K562	blood:	n/a	n/a
30	CEBPB	chr13:92970428-92970745	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr13:92955779-92956034	IMR90	lung:	n/a	chr13:92955901-92955912
32	CEBPB	chr13:92955819-92956028	HepG2	liver:	n/a	chr13:92955901-92955912
33	CEBPB	chr13:92955774-92956106	K562	blood:	n/a	chr13:92955901-92955912
34	CEBPB	chr13:92965732-92965919	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr13:92955817-92956017	A549	lung:	n/a	chr13:92955901-92955912
36	CEBPB	chr13:92960630-92960977	K562	blood:	n/a	chr13:92960815-92960826
37	CHD2	chr13:93020251-93020278	K562	blood:	n/a	n/a
38	CTCF	chr13:93007540-93007690	HCM	heart:	n/a	n/a
39	CTCF	chr13:93007580-93007730	HepG2	liver:	n/a	n/a
40	CTCF	chr13:93007336-93007958	K562	blood:	n/a	n/a
41	CTCF	chr13:93007580-93007730	HAc	cerebellar:	n/a	n/a
42	CTCF	chr13:93007600-93007750	HCM	heart:	n/a	n/a
43	CTCF	chr13:93007574-93007778	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr13:93007640-93007790	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr13:93007579-93007758	Lung_OC	lung:	n/a	n/a
46	CTCF	chr13:93007542-93007808	LNCaP	prostate:	n/a	n/a
47	CTCF	chr13:93007560-93007710	HCFaa	heart:	n/a	n/a
48	CTCF	chr13:93007580-93007730	HPF	lung:	n/a	n/a
49	CTCF	chr13:93007600-93007750	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr13:93030052-93030694	K562	blood:	n/a	chr13:93030341-93030359

No data

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:93035931..93038360-chr13:93040380..93042360,2	K562	blood:
2	chr13:92956827..92958387-chr13:92959759..92961351,2	K562	blood:
3	chr13:93018970..93021048-chr13:93021164..93022779,2	K562	blood:
4	chr13:93024437..93027101-chr13:93028065..93030296,2	K562	blood:
5	chr13:92995861..92998163-chr13:93022468..93024947,2	K562	blood:
6	chr13:93026561..93029613-chr13:93041707..93044561,3	K562	blood:
7	chr13:93012828..93015636-chr13:93017565..93019548,2	K562	blood:
8	chr13:92962787..92965087-chr13:92966991..92969071,2	K562	blood:
9	chr13:93012828..93015636-chr13:93017565..93019548,2	K562	blood:
10	chr13:93036860..93038900-chr13:93040380..93043819,4	K562	blood:
11	chr13:93013213..93015773-chr13:93023566..93027348,3	K562	blood:
12	chr13:92995861..92998163-chr13:93022468..93024947,2	K562	blood:
13	chr13:93028655..93031669-chr13:93033790..93037106,3	K562	blood:
14	chr13:92984785..92987410-chr13:92992278..92995322,3	K562	blood:
15	chr13:92951893..92954281-chr13:92957574..92960507,2	K562	blood:
16	chr13:92981004..92983533-chr13:93023966..93025848,2	K562	blood:
17	chr13:93029774..93033381-chr13:93039131..93043022,5	K562	blood:
18	chr13:92957176..92958871-chr13:92997001..92998891,2	K562	blood:
19	chr13:92951893..92954281-chr13:92957574..92960507,2	K562	blood:
20	chr13:92958679..92961533-chr13:93089880..93091566,2	K562	blood:
21	chr13:93033779..93037565-chr13:93037863..93040159,3	K562	blood:
22	chr13:93013213..93015773-chr13:93023566..93027348,3	K562	blood:
23	chr13:92964628..92966987-chr13:92977426..92979496,2	K562	blood:
24	chr13:92981004..92983533-chr13:93023966..93025848,2	K562	blood:
25	chr13:93031583..93033539-chr13:94000749..94002746,2	K562	blood:
26	chr13:93029053..93031033-chr13:93035454..93037106,2	K562	blood:
27	chr13:92964628..92966987-chr13:92977426..92979496,2	K562	blood:
28	chr13:92982264..92985131-chr13:93004741..93006675,2	K562	blood:
29	chr13:92983145..92985904-chr13:92987086..92990641,3	K562	blood:
30	chr13:92986047..92988836-chr13:93080866..93083328,2	K562	blood:
31	chr13:92983817..92985368-chr13:93015068..93017856,2	K562	blood:
32	chr13:93024752..93026535-chr13:93034305..93036660,2	K562	blood:
33	chr13:93033779..93037565-chr13:93037863..93040159,3	K562	blood:
34	chr13:92968259..92969910-chr13:92996026..92998901,2	K562	blood:
35	chr13:93029774..93033381-chr13:93039131..93043022,5	K562	blood:
36	chr13:92982264..92985131-chr13:93004741..93006675,2	K562	blood:
37	chr13:92961385..92963031-chr13:92979111..92982076,2	K562	blood:
38	chr13:92968259..92969910-chr13:92996026..92998901,2	K562	blood:
39	chr13:92987424..92989331-chr13:92989713..92992513,2	K562	blood:
40	chr13:92965487..92967711-chr13:92976361..92978926,2	K562	blood:
41	chr13:92970236..92973225-chr13:92975344..92980353,5	K562	blood:
42	chr13:93004690..93006667-chr13:93012295..93015000,2	K562	blood:
43	chr13:92956827..92958387-chr13:92959759..92961351,2	K562	blood:
44	chr13:92983145..92985904-chr13:92987086..92990641,3	K562	blood:
45	chr13:93018970..93021048-chr13:93021164..93022779,2	K562	blood:
46	chr13:92957496..92960008-chr13:92963128..92965362,2	K562	blood:
47	chr13:92985419..92987954-chr13:93220833..93223543,2	K562	blood:
48	chr13:92970236..92973225-chr13:92975344..92980353,5	K562	blood:
49	chr13:92965451..92968338-chr13:92972669..92975627,2	K562	blood:
50	chr13:92965487..92967711-chr13:92976361..92978926,2	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: 1264 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1926624	chr13:92953101-92953102	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141986972	chr13:92953111-92953112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559160676	chr13:92953163-92953164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528277313	chr13:92953167-92953168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185286569	chr13:92953177-92953178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376620992	chr13:92953285-92953286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71427554	chr13:92953351-92953352	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs150895883	chr13:92953421-92953422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530899758	chr13:92953427-92953428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542541002	chr13:92953464-92953465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552746396	chr13:92953465-92953466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572740226	chr13:92953488-92953489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12877979	chr13:92953497-92953498	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs74911966	chr13:92953506-92953507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114827932	chr13:92953559-92953560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs9301792	chr13:92953562-92953563	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs377431094	chr13:92953575-92953576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147571339	chr13:92953598-92953599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530417082	chr13:92953675-92953676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74107173	chr13:92953711-92953712	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs16947286	chr13:92953728-92953729	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541187854	chr13:92953751-92953752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376606675	chr13:92953755-92953756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188601385	chr13:92953777-92953778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547327304	chr13:92953778-92953779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569459519	chr13:92954412-92954413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530517605	chr13:92954417-92954418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550690591	chr13:92954444-92954445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs202184868	chr13:92954481-92954482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9284270	chr13:92954491-92954492	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs144344031	chr13:92954499-92954500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35945873	chr13:92954520-92954521	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs566414944	chr13:92954548-92954549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538952588	chr13:92954559-92954560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569131125	chr13:92954567-92954568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558471548	chr13:92954591-92954592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575438797	chr13:92954621-92954622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530956836	chr13:92954727-92954728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537656560	chr13:92954733-92954734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555003240	chr13:92954737-92954738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191954284	chr13:92954773-92954774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35392830	chr13:92954804-92954805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184197174	chr13:92954810-92954811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544586729	chr13:92954848-92954849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77144641	chr13:92954853-92954854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560502300	chr13:92954887-92954888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528929187	chr13:92954931-92954932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577589179	chr13:92954945-92954946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546522555	chr13:92954970-92954971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187202068	chr13:92955005-92955006	Enhancers	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:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92952400-92953800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:92953200-92953600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:92954400-92956200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:92955600-92956200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr13:92958600-92959000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr13:92958600-92959000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr13:92958600-92959000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr13:92958800-92959200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr13:92960000-92960600	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr13:92965800-92966000	Enhancers	Ovary	ovary
11	chr13:92965800-92966200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr13:92966400-92966600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr13:92966600-92967600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr13:92967000-92967400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr13:92967400-92969400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:92967600-92967800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:92967600-92968000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr13:92967600-92968400	Enhancers	NH-A	brain
19	chr13:92968000-92969200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr13:92968000-92969800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr13:92968400-92968800	Weak transcription	NH-A	brain
22	chr13:92968800-92970000	Enhancers	NH-A	brain
23	chr13:92969200-92969800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr13:92969400-92969800	Enhancers	Fetal Lung	lung
25	chr13:92969400-92970000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr13:92969400-92970000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:92969400-92970000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:92969800-92970200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr13:92969800-92972600	Weak transcription	Fetal Lung	lung
30	chr13:92970200-92971200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:92971200-92971400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr13:92972600-92972800	Enhancers	Fetal Lung	lung
33	chr13:92972800-92973200	Weak transcription	Fetal Lung	lung
34	chr13:92973200-92974000	Enhancers	Fetal Lung	lung
35	chr13:92978800-92980000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr13:92980800-92981600	Enhancers	Pancreas	Pancrea
37	chr13:92981600-92983000	Weak transcription	Pancreas	Pancrea
38	chr13:92983000-92983200	Enhancers	Pancreas	Pancrea
39	chr13:92983400-92984200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:92983600-92984600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr13:92994400-92998200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr13:92997800-92998800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr13:92997800-92998800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr13:92998000-92998400	Enhancers	Adipose Nuclei	Adipose
45	chr13:92998200-92998600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr13:92998200-92998600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:92998200-92998600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr13:92998200-92998800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr13:92998200-92999000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr13:92998400-92998600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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