Variant report

Variant	nsv562633
Chromosome Location	chr13:88871759-88980273
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	CEBPB	chr13:88889709-88890026	IMR90	lung:	n/a	n/a
2	CEBPB	chr13:88969442-88969662	A549	lung:	n/a	chr13:88969510-88969523 chr13:88969510-88969521 chr13:88969512-88969523 chr13:88969510-88969523
3	CEBPB	chr13:88969361-88969684	HepG2	liver:	n/a	chr13:88969510-88969523 chr13:88969510-88969521 chr13:88969512-88969523 chr13:88969510-88969523
4	CHD2	chr13:88937800-88937820	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr13:88925835-88925880	Medullo	brain:	n/a	n/a
6	CTCF	chr13:88946218-88946268	GM13976	blood:	n/a	n/a
7	CTCF	chr13:88944299-88944375	GM10266	blood:	n/a	n/a
8	CTCF	chr13:88957631-88957693	IMR90	lung:	n/a	n/a
9	CTCF	chr13:88900480-88900630	AG10803	skin:	n/a	n/a
10	CTCF	chr13:88962180-88962330	HRE	kidney:	n/a	n/a
11	CTCF	chr13:88962541-88962621	Kidney_OC	kidney:	n/a	n/a
12	E2F4	chr13:88914368-88914568	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr13:88924522-88924658	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr13:88902589-88902912	MCF10A-Er-Src	breast:	n/a	chr13:88902762-88902773 chr13:88902759-88902770 chr13:88902763-88902772
15	FOS	chr13:88924726-88924957	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr13:88902604-88902938	MCF10A-Er-Src	breast:	n/a	chr13:88902762-88902773 chr13:88902759-88902770 chr13:88902763-88902772
17	FOS	chr13:88941870-88942151	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr13:88941920-88942120	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr13:88902605-88902935	MCF10A-Er-Src	breast:	n/a	chr13:88902762-88902773 chr13:88902759-88902770 chr13:88902763-88902772
20	FOS	chr13:88941888-88942117	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr13:88924666-88924974	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr13:88902631-88902903	MCF10A-Er-Src	breast:	n/a	chr13:88902762-88902773 chr13:88902759-88902770 chr13:88902763-88902772
23	FOS	chr13:88924666-88924897	MCF10A-Er-Src	breast:	n/a	n/a
24	GATA3	chr13:88979251-88979696	SH-SY5Y	brain:	n/a	n/a
25	HEY1	chr13:88944926-88945151	K562	blood:	n/a	n/a
26	IRF1	chr13:88958767-88958899	K562	blood:	n/a	n/a
27	JUN	chr13:88925956-88926156	K562	blood:	n/a	n/a
28	JUN	chr13:88935699-88935731	HepG2	liver:	n/a	chr13:88935708-88935721
29	JUN	chr13:88925691-88925805	H1-hESC	embryonic stem cell:	n/a	n/a
30	JUND	chr13:88902762-88902789	H1-hESC	embryonic stem cell:	n/a	chr13:88902762-88902773 chr13:88902763-88902772
31	KAP1	chr13:88898546-88899107	HEK293	kidney:	n/a	n/a
32	KAP1	chr13:88937694-88937975	HEK293	kidney:	n/a	n/a
33	KAP1	chr13:88956389-88956753	HEK293	kidney:	n/a	n/a
34	MAFF	chr13:88971049-88971110	HepG2	liver:	n/a	chr13:88971085-88971103
35	MAFF	chr13:88970048-88970232	HepG2	liver:	n/a	n/a
36	MAFF	chr13:88881374-88881921	HepG2	liver:	n/a	chr13:88881741-88881759 chr13:88881772-88881790
37	MAFF	chr13:88916163-88916363	K562	blood:	n/a	chr13:88916261-88916279
38	MAFF	chr13:88916114-88916424	HepG2	liver:	n/a	chr13:88916261-88916279
39	MAFK	chr13:88970038-88970256	HepG2	liver:	n/a	n/a
40	MAFK	chr13:88881479-88881518	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAFK	chr13:88976168-88976196	H1-hESC	embryonic stem cell:	n/a	n/a
42	MAFK	chr13:88916085-88916427	HepG2	liver:	n/a	chr13:88916262-88916277
43	MAFK	chr13:88971020-88971210	IMR90	lung:	n/a	chr13:88971090-88971101 chr13:88971086-88971102 chr13:88971089-88971103 chr13:88971086-88971101
44	MAFK	chr13:88916217-88916417	H1-hESC	embryonic stem cell:	n/a	chr13:88916262-88916277
45	MAFK	chr13:88912777-88912831	HepG2	liver:	n/a	n/a
46	MAFK	chr13:88916085-88916423	IMR90	lung:	n/a	chr13:88916262-88916277
47	MAFK	chr13:88881367-88881907	HepG2	liver:	n/a	chr13:88881520-88881535
48	MAFK	chr13:88881439-88881897	HepG2	liver:	n/a	chr13:88881520-88881535
49	MAFK	chr13:88916108-88916441	HepG2	liver:	n/a	chr13:88916262-88916277
50	MAFK	chr13:88970981-88971238	HepG2	liver:	n/a	chr13:88971090-88971101 chr13:88971086-88971102 chr13:88971089-88971103 chr13:88971086-88971101

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:88944177-88944227	CMK	blood:	n/a
2	chr13:88944177-88944227	GM06990	blood:	n/a
3	chr13:88944177-88944227	ProgFib	skin:	n/a
4	chr13:88944177-88944227	HMEC	breast:	n/a
5	chr13:88944177-88944227	NB4	blood:	n/a
6	chr13:88944177-88944227	GM12878	blood:	n/a
7	chr13:88944177-88944227	HAEpiC	amniotic membrane:	n/a
8	chr13:88944177-88944227	Caco-2	colon:	n/a
9	chr13:88944177-88944227	HepG2	liver:	n/a
10	chr13:88944177-88944227	SK-N-SH	brain:	n/a
11	chr13:88944177-88944227	HCM	heart:	n/a
12	chr13:88944177-88944227	NH-A	brain:	n/a
13	chr13:88944177-88944227	K562	blood:	n/a
14	chr13:88944177-88944227	HCPEpiC	choroid plexus:	n/a
15	chr13:88944177-88944227	U87	brain:	n/a
16	chr13:88944177-88944227	HIPEpiC	eye:	n/a
17	chr13:88944177-88944227	GM19239	blood:	n/a
18	chr13:88944177-88944227	LNCaP	prostate:	n/a
19	chr13:88944177-88944227	HCF	heart:	n/a
20	chr13:88944177-88944227	Hela-S3	cervix:	n/a
21	chr13:88944177-88944227	PFSK-1	brain:	n/a
22	chr13:88944177-88944227	HEK293	kidney:	embryo
23	chr13:88944177-88944227	H1-hESC	embryonic stem cell:	embryo
24	chr13:88944177-88944227	GM12892	blood:	n/a
25	chr13:88944177-88944227	AG04450	lung:	fetal
26	chr13:88944177-88944227	HPAEpiC	pulmonary alveolar:	n/a
27	chr13:88944177-88944227	NHBE	bronchial:	n/a
28	chr13:88944177-88944227	RPTEC	kidney:	n/a
29	chr13:88944177-88944227	PANC-1	pancreas:	n/a
30	chr13:88944177-88944227	MCF10A-Er-Src	breast:	n/a
31	chr13:88944177-88944227	HRCEpiC	kidney:	n/a
32	chr13:88944177-88944227	HEEpiC	esophagus:	n/a
33	chr13:88944177-88944227	HNPCEpiC	eye:	n/a
34	chr13:88944177-88944227	SKMC	muscle:	n/a
35	chr13:88944177-88944227	AG04449	skin:	fetal
36	chr13:88944177-88944227	AG10803	skin:	n/a
37	chr13:88944177-88944227	ECC-1	luminal epithelium:	n/a
38	chr13:88944177-88944227	AG09319	gingival:	n/a
39	chr13:88944177-88944227	NHDF-neo	bronchial:	n/a
40	chr13:88944177-88944227	IMR90	lung:	fetal
41	chr13:88944177-88944227	HCT-116	colon:	n/a
42	chr13:88944177-88944227	HRPEpiC	eye:	n/a
43	chr13:88944177-88944227	MCF-7	breast:	n/a
44	chr13:88944177-88944227	AoSMC	blood vessel:	n/a
45	chr13:88944177-88944227	SK-N-MC	brain:	n/a
46	chr13:88944177-88944227	Jurkat	blood:	n/a
47	chr13:88944177-88944227	BJ	skin:	n/a
48	chr13:88944177-88944227	SK-N-SH_RA	brain:	n/a
49	chr13:88944177-88944227	HUVEC	blood vessel:	n/a
50	chr13:88944177-88944227	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:88973778..88975590-chr13:88975862..88978691,2	MCF-7	breast:
2	chr13:88917657..88918177-chr6:157007973..157008592,2	Hela-S3	cervix:
3	chr13:88973778..88975590-chr13:88975862..88978691,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-18	chr13:88888802-88889224	NONHSAT034610
2	lnc-SLITRK6-19	chr13:88950629-88950764	NONHSAT034611
3	lnc-SLITRK6-19	chr13:88927863-88928392	NONHSAT034611
4	lnc-SLITRK5-5	chr13:88886578-88886673	ENSG00000231019
5	lnc-SLITRK5-5	chr13:88888258-88888337	ENSG00000231019

Variant related genes	Relation type
RPL29P29	TF binding region
RPL29P29	CpG island

Extended variants
information (count: 708 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36087467	chr13:88886652-88886653	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs536708311	chr13:88888264-88888265	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs555120150	chr13:88888274-88888275	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs114232272	chr13:88888291-88888292	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs61959429	chr13:88888319-88888320	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs546301448	chr13:88888825-88888826	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs4772705	chr13:88888991-88888992	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs181301203	chr13:88889017-88889018	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs58920470	chr13:88889043-88889044	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs577451760	chr13:88889050-88889051	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs184934650	chr13:88889051-88889052	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs142582719	chr13:88889065-88889066	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs552782840	chr13:88889066-88889067	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs574049091	chr13:88889114-88889115	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs189827357	chr13:88889165-88889166	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs180983175	chr13:88889186-88889187	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs559026651	chr13:88889709-88889710	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs61959432	chr13:88889713-88889714	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs538437655	chr13:88889735-88889736	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs556400229	chr13:88889767-88889768	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs9514491	chr13:88889784-88889785	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190981401	chr13:88889787-88889788	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs149054962	chr13:88889799-88889800	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553385045	chr13:88889877-88889878	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572021715	chr13:88889888-88889889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs545549251	chr13:88889947-88889948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs181730908	chr13:88889973-88889974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs185909746	chr13:88889990-88889991	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs543684599	chr13:88890012-88890013	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs561962451	chr13:88890018-88890019	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs529235504	chr13:88890024-88890025	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs543622996	chr13:88890521-88890522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556116353	chr13:88890952-88890953	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs112308205	chr13:88891023-88891024	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs116106643	chr13:88892128-88892129	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs370329574	chr13:88892159-88892160	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs61959449	chr13:88892160-88892161	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs543075285	chr13:88892205-88892206	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs559603510	chr13:88892232-88892233	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs529376225	chr13:88892260-88892261	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs180813731	chr13:88892702-88892703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs543296169	chr13:88893523-88893524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200830855	chr13:88893570-88893571	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs59079304	chr13:88893572-88893573	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs72196279	chr13:88893573-88893574	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs185341811	chr13:88893595-88893596	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs55822243	chr13:88893605-88893606	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs111701598	chr13:88898446-88898447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532956065	chr13:88898469-88898470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551424642	chr13:88898483-88898484	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	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
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Non-small cell lung cancer	16651412	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:88898400-88898600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr13:88898600-88898800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:88898800-88900400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr13:88900200-88901000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:88900400-88901200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr13:88900400-88901200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr13:88900400-88901400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr13:88900400-88901400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr13:88900600-88901000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr13:88900600-88901400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr13:88901200-88902000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr13:88901400-88902400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr13:88901400-88902600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr13:88902600-88902800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr13:88902600-88902800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr13:88902800-88903000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr13:88902800-88905400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr13:88906200-88906400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:88909200-88909600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:88918400-88920000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr13:88919000-88919600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr13:88919600-88923200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr13:88923200-88923400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr13:88923200-88923600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr13:88923400-88923800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr13:88923800-88924200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr13:88937600-88938600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
28	chr13:88955400-88955600	Enhancers	Primary B cells from peripheral blood	blood
29	chr13:88955600-88955800	Enhancers	Primary B cells from cord blood	blood
30	chr13:88955600-88956000	Active TSS	Primary B cells from peripheral blood	blood
31	chr13:88955600-88956200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr13:88955800-88956200	Flanking Active TSS	Primary B cells from cord blood	blood
33	chr13:88956000-88957000	Enhancers	Primary B cells from peripheral blood	blood
34	chr13:88956200-88956600	Enhancers	Primary B cells from cord blood	blood
35	chr13:88970400-88970600	Enhancers	Pancreas	Pancrea
36	chr13:88972200-88973000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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