Variant report

Variant	nsv562727
Chromosome Location	chr13:92961151-93038913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:438)
CpG islands
(count:0)
Chromatin interactive
region (count:62)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:438 , 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	ARID3A	chr13:93007422-93007801	K562	blood:	n/a	n/a
2	ATF1	chr13:93018071-93018476	K562	blood:	n/a	n/a
3	ATF1	chr13:92977355-92978161	K562	blood:	n/a	n/a
4	ATF1	chr13:92971259-92971965	K562	blood:	n/a	n/a
5	ATF1	chr13:92988289-92989010	K562	blood:	n/a	n/a
6	ATF1	chr13:93033932-93034002	K562	blood:	n/a	n/a
7	ATF1	chr13:92989310-92989318	K562	blood:	n/a	n/a
8	ATF1	chr13:92991024-92991295	K562	blood:	n/a	n/a
9	ATF1	chr13:92985734-92986088	K562	blood:	n/a	n/a
10	ATF1	chr13:93008905-93009443	K562	blood:	n/a	n/a
11	ATF1	chr13:92989785-92989940	K562	blood:	n/a	n/a
12	ATF1	chr13:93023686-93024321	K562	blood:	n/a	n/a
13	ATF1	chr13:92969411-92969828	K562	blood:	n/a	n/a
14	ATF1	chr13:92976143-92976957	K562	blood:	n/a	n/a
15	ATF1	chr13:93000542-93000602	K562	blood:	n/a	n/a
16	ATF1	chr13:92973596-92973794	K562	blood:	n/a	n/a
17	BACH1	chr13:92998581-92998621	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr13:93011566-93011568	K562	blood:	n/a	n/a
19	BATF	chr13:92967550-92967856	GM12878	blood:	n/a	chr13:92967690-92967701
20	BATF	chr13:92967590-92967851	GM12878	blood:	n/a	chr13:92967690-92967701
21	BCL11A	chr13:92967565-92967763	GM12878	blood:	n/a	n/a
22	BHLHE40	chr13:93007542-93007875	K562	blood:	n/a	n/a
23	BHLHE40	chr13:93032155-93032279	K562	blood:	n/a	n/a
24	CCNT2	chr13:92976086-92976237	K562	blood:	n/a	n/a
25	CCNT2	chr13:93018008-93018434	K562	blood:	n/a	n/a
26	CCNT2	chr13:92991177-92991375	K562	blood:	n/a	n/a
27	CEBPB	chr13:92970428-92970745	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr13:92965732-92965919	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr13:93020251-93020278	K562	blood:	n/a	n/a
30	CTCF	chr13:93007600-93007750	BE2_C	brain:	n/a	n/a
31	CTCF	chr13:93007660-93007810	NHEK	skin:	n/a	n/a
32	CTCF	chr13:93007562-93007793	MCF-7	breast:	n/a	n/a
33	CTCF	chr13:93032248-93032260	K562	blood:	n/a	n/a
34	CTCF	chr13:93007526-93007778	IMR90	lung:	n/a	n/a
35	CTCF	chr13:93007560-93007710	A549	lung:	n/a	n/a
36	CTCF	chr13:93007600-93007750	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr13:93030260-93030410	HCM	heart:	n/a	chr13:93030341-93030359
38	CTCF	chr13:93007600-93007750	HRE	kidney:	n/a	n/a
39	CTCF	chr13:93007500-93007650	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr13:93007646-93007748	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr13:93007580-93007730	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr13:93033560-93033710	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr13:92976758-92976770	K562	blood:	n/a	n/a
44	CTCF	chr13:93007369-93008074	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr13:93007500-93007650	HVMF	connective:	n/a	n/a
46	CTCF	chr13:93007415-93007841	T-47D	breast:	n/a	n/a
47	CTCF	chr13:93007467-93007798	MCF-7	breast:	n/a	n/a
48	CTCF	chr13:93007580-93007730	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr13:93007600-93007750	HPF	lung:	n/a	n/a
50	CTCF	chr13:93007543-93007786	LNCaP	prostate:	n/a	n/a

No data

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:93018970..93021048-chr13:93021164..93022779,2	K562	blood:
2	chr13:92980924..92984645-chr13:92987086..92990340,3	K562	blood:
3	chr13:92961385..92963031-chr13:92979111..92982076,2	K562	blood:
4	chr13:93028655..93031669-chr13:93033790..93037106,3	K562	blood:
5	chr13:92981004..92983533-chr13:93023966..93025848,2	K562	blood:
6	chr13:93028655..93031669-chr13:93033790..93037106,3	K562	blood:
7	chr13:92968259..92969910-chr13:92996026..92998901,2	K562	blood:
8	chr13:93013213..93015773-chr13:93023566..93027348,3	K562	blood:
9	chr13:92956827..92958387-chr13:92959759..92961351,2	K562	blood:
10	chr13:92962787..92965087-chr13:92966991..92969071,2	K562	blood:
11	chr13:93012828..93015636-chr13:93017565..93019548,2	K562	blood:
12	chr13:93031583..93033539-chr13:94000749..94002746,2	K562	blood:
13	chr13:92965451..92968338-chr13:92972669..92975627,2	K562	blood:
14	chr13:92981004..92983533-chr13:93023966..93025848,2	K562	blood:
15	chr13:92965451..92968338-chr13:92972669..92975627,2	K562	blood:
16	chr13:92982264..92985131-chr13:93004741..93006675,2	K562	blood:
17	chr13:92957176..92958871-chr13:92997001..92998891,2	K562	blood:
18	chr13:92961385..92963031-chr13:92979111..92982076,2	K562	blood:
19	chr13:93029053..93031033-chr13:93035454..93037106,2	K562	blood:
20	chr13:92841987..92842813-chr13:93007626..93008163,2	MCF-7	breast:
21	chr13:92970236..92973225-chr13:92975344..92980353,5	K562	blood:
22	chr13:92957496..92960008-chr13:92963128..92965362,2	K562	blood:
23	chr13:92970236..92973225-chr13:92975344..92980353,5	K562	blood:
24	chr13:92968259..92969910-chr13:92996026..92998901,2	K562	blood:
25	chr13:92985419..92987954-chr13:93220833..93223543,2	K562	blood:
26	chr13:93012828..93015636-chr13:93017565..93019548,2	K562	blood:
27	chr13:92964628..92966987-chr13:92977426..92979496,2	K562	blood:
28	chr13:92995861..92998163-chr13:93022468..93024947,2	K562	blood:
29	chr13:93024437..93027101-chr13:93028065..93030296,2	K562	blood:
30	chr13:92984785..92987410-chr13:92992278..92995322,3	K562	blood:
31	chr13:92987424..92989331-chr13:92989713..92992513,2	K562	blood:
32	chr13:93024752..93026535-chr13:93034305..93036660,2	K562	blood:
33	chr13:92983145..92985904-chr13:92987086..92990641,3	K562	blood:
34	chr13:92983817..92985368-chr13:93015068..93017856,2	K562	blood:
35	chr13:92983817..92985368-chr13:93015068..93017856,2	K562	blood:
36	chr13:93029053..93031033-chr13:93035454..93037106,2	K562	blood:
37	chr13:92010706..92013622-chr13:93006752..93008493,2	K562	blood:
38	chr13:93035931..93038360-chr13:93040380..93042360,2	K562	blood:
39	chr13:92965487..92967711-chr13:92976361..92978926,2	K562	blood:
40	chr13:92987424..92989331-chr13:92989713..92992513,2	K562	blood:
41	chr13:92965487..92967711-chr13:92976361..92978926,2	K562	blood:
42	chr13:93004690..93006667-chr13:93012295..93015000,2	K562	blood:
43	chr13:93024437..93027101-chr13:93028065..93030296,2	K562	blood:
44	chr13:93024752..93026535-chr13:93034305..93036660,2	K562	blood:
45	chr13:93036860..93038900-chr13:93040380..93043819,4	K562	blood:
46	chr13:93033779..93037565-chr13:93037863..93040159,3	K562	blood:
47	chr13:92982264..92985131-chr13:93004741..93006675,2	K562	blood:
48	chr13:93018970..93021048-chr13:93021164..93022779,2	K562	blood:
49	chr13:93033779..93037565-chr13:93037863..93040159,3	K562	blood:
50	chr13:93029774..93033381-chr13:93039131..93043022,5	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: 1115 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16947347	chr13:92965821-92965822	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75700967	chr13:92965843-92965844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369168047	chr13:92965848-92965849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190477324	chr13:92965857-92965858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76747930	chr13:92965871-92965872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372600145	chr13:92965901-92965902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs180742078	chr13:92965929-92965930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558375274	chr13:92965944-92965945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186062224	chr13:92965949-92965950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536063236	chr13:92965958-92965959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146022479	chr13:92965960-92965961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573272128	chr13:92965978-92965979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9589499	chr13:92965986-92965987	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs189829297	chr13:92966043-92966044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77443718	chr13:92966066-92966067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574969388	chr13:92966078-92966079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181323951	chr13:92966086-92966087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139973178	chr13:92966087-92966088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570852044	chr13:92966103-92966104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185510368	chr13:92966111-92966112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs80141438	chr13:92966136-92966137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs61607987	chr13:92966153-92966154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9584014	chr13:92966163-92966164	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs550961626	chr13:92966173-92966174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375512410	chr13:92966400-92966401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536413164	chr13:92966446-92966447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552927448	chr13:92966461-92966462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190304418	chr13:92966494-92966495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572435693	chr13:92966502-92966503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371211564	chr13:92966551-92966552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534906388	chr13:92966552-92966553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566952897	chr13:92966562-92966563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558372705	chr13:92966564-92966565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374223934	chr13:92966609-92966610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538796884	chr13:92966633-92966634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377662855	chr13:92966641-92966642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559101605	chr13:92966712-92966713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182951450	chr13:92966735-92966736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370689398	chr13:92966815-92966816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78949362	chr13:92966816-92966817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73629661	chr13:92966853-92966854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61966638	chr13:92966867-92966868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368059000	chr13:92966911-92966912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187237578	chr13:92966934-92966935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368333866	chr13:92966960-92966961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560571249	chr13:92967014-92967015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192067707	chr13:92967020-92967021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544665664	chr13:92967023-92967024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562591977	chr13:92967033-92967034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143331086	chr13:92967035-92967036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92965800-92966000	Enhancers	Ovary	ovary
2	chr13:92965800-92966200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:92966400-92966600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr13:92966600-92967600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr13:92967000-92967400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:92967400-92969400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:92967600-92967800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:92967600-92968000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr13:92967600-92968400	Enhancers	NH-A	brain
10	chr13:92968000-92969200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:92968000-92969800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr13:92968400-92968800	Weak transcription	NH-A	brain
13	chr13:92968800-92970000	Enhancers	NH-A	brain
14	chr13:92969200-92969800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr13:92969400-92969800	Enhancers	Fetal Lung	lung
16	chr13:92969400-92970000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr13:92969400-92970000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr13:92969400-92970000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr13:92969800-92970200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr13:92969800-92972600	Weak transcription	Fetal Lung	lung
21	chr13:92970200-92971200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr13:92971200-92971400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr13:92972600-92972800	Enhancers	Fetal Lung	lung
24	chr13:92972800-92973200	Weak transcription	Fetal Lung	lung
25	chr13:92973200-92974000	Enhancers	Fetal Lung	lung
26	chr13:92978800-92980000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr13:92980800-92981600	Enhancers	Pancreas	Pancrea
28	chr13:92981600-92983000	Weak transcription	Pancreas	Pancrea
29	chr13:92983000-92983200	Enhancers	Pancreas	Pancrea
30	chr13:92983400-92984200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:92983600-92984600	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr13:92994400-92998200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr13:92997800-92998800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:92997800-92998800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr13:92998000-92998400	Enhancers	Adipose Nuclei	Adipose
36	chr13:92998200-92998600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr13:92998200-92998600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr13:92998200-92998600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr13:92998200-92998800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr13:92998200-92999000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr13:92998400-92998600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:92998400-92998800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr13:93009800-93011800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr13:93015000-93015600	Enhancers	Fetal Heart	heart
45	chr13:93015200-93015600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr13:93015400-93015800	Enhancers	Fetal Stomach	stomach
47	chr13:93031200-93032000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr13:93031400-93031800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr13:93036200-93037200	Enhancers	Pancreatic Islets	Pancreatic Islet

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