Variant report

Variant	esv2757546
Chromosome Location	chr13:89539415-89864593
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	ATF2	chr13:89572186-89572643	GM12878	blood:	n/a	n/a
2	ATF2	chr13:89572207-89572528	GM12878	blood:	n/a	n/a
3	BACH1	chr13:89705066-89705214	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:89623437-89623444	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr13:89561544-89561732	GM12878	blood:	n/a	n/a
6	BATF	chr13:89572277-89572559	GM12878	blood:	n/a	n/a
7	BATF	chr13:89572273-89572568	GM12878	blood:	n/a	n/a
8	BCL11A	chr13:89572223-89572570	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:89643606-89643700	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:89714096-89714420	HepG2	liver:	n/a	n/a
11	BHLHE40	chr13:89632073-89632317	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:89572310-89572510	GM12878	blood:	n/a	n/a
13	BRCA1	chr13:89809033-89809039	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr13:89751122-89751322	HepG2	liver:	n/a	chr13:89751225-89751236
15	CEBPB	chr13:89751096-89751336	IMR90	lung:	n/a	chr13:89751225-89751236
16	CEBPB	chr13:89734912-89735227	ECC-1	luminal epithelium:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
17	CEBPB	chr13:89598017-89598337	ECC-1	luminal epithelium:	n/a	chr13:89598238-89598249
18	CEBPB	chr13:89734904-89735256	Hela-S3	cervix:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
19	CEBPB	chr13:89788283-89788664	HepG2	liver:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
20	CEBPB	chr13:89751133-89751376	A549	lung:	n/a	chr13:89751225-89751236
21	CEBPB	chr13:89598055-89598434	IMR90	lung:	n/a	chr13:89598238-89598249
22	CEBPB	chr13:89788251-89788403	K562	blood:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
23	CEBPB	chr13:89734887-89735255	A549	lung:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
24	CEBPB	chr13:89687704-89688097	HepG2	liver:	n/a	chr13:89687872-89687883
25	CEBPB	chr13:89734894-89735243	IMR90	lung:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
26	CEBPB	chr13:89630896-89631259	IMR90	lung:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
27	CEBPB	chr13:89598032-89598441	A549	lung:	n/a	chr13:89598238-89598249
28	CEBPB	chr13:89630955-89631172	K562	blood:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
29	CEBPB	chr13:89630897-89631243	HepG2	liver:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
30	CEBPB	chr13:89630930-89631228	H1-hESC	embryonic stem cell:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
31	CEBPB	chr13:89598071-89598408	K562	blood:	n/a	chr13:89598238-89598249
32	CEBPB	chr13:89823580-89823834	HepG2	liver:	n/a	chr13:89823710-89823721
33	CEBPB	chr13:89598060-89598453	ECC-1	luminal epithelium:	n/a	chr13:89598238-89598249
34	CEBPB	chr13:89596083-89596253	HepG2	liver:	n/a	chr13:89596117-89596128 chr13:89596118-89596129
35	CEBPB	chr13:89785424-89785641	HepG2	liver:	n/a	chr13:89785500-89785517
36	CEBPB	chr13:89630916-89631254	A549	lung:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
37	CEBPB	chr13:89719069-89719489	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr13:89856664-89857107	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
39	CEBPB	chr13:89856691-89857129	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
40	CEBPB	chr13:89707272-89707463	HepG2	liver:	n/a	n/a
41	CEBPB	chr13:89734889-89735264	ECC-1	luminal epithelium:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
42	CEBPB	chr13:89598063-89598417	A549	lung:	n/a	chr13:89598238-89598249
43	CEBPB	chr13:89816073-89816273	HepG2	liver:	n/a	chr13:89816134-89816145 chr13:89816156-89816167
44	CEBPB	chr13:89598062-89598418	H1-hESC	embryonic stem cell:	n/a	chr13:89598238-89598249
45	CEBPB	chr13:89598067-89598413	Hela-S3	cervix:	n/a	chr13:89598238-89598249
46	CEBPB	chr13:89751155-89751382	Hela-S3	cervix:	n/a	chr13:89751225-89751236
47	CEBPB	chr13:89539359-89539639	HepG2	liver:	n/a	n/a
48	CEBPB	chr13:89734909-89735246	H1-hESC	embryonic stem cell:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
49	CEBPB	chr13:89734962-89735178	K562	blood:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
50	CEBPB	chr13:89598062-89598430	HepG2	liver:	n/a	chr13:89598238-89598249

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89815421-89815471	CMK	blood:	n/a
2	chr13:89815451-89815501	GM12891	blood:	n/a
3	chr13:89815421-89815471	SK-N-SH	brain:	n/a
4	chr13:89740340-89740390	GM12891	blood:	n/a
5	chr13:89815451-89815501	T-47D	breast:	n/a
6	chr13:89740340-89740390	HCT-116	colon:	n/a
7	chr13:89815421-89815471	MCF-7	breast:	n/a
8	chr13:89815451-89815501	Jurkat	blood:	n/a
9	chr13:89815421-89815471	HEEpiC	esophagus:	n/a
10	chr13:89740340-89740390	GM19239	blood:	n/a
11	chr13:89740340-89740390	SK-N-SH_RA	brain:	n/a
12	chr13:89815421-89815471	U87	brain:	n/a
13	chr13:89740340-89740390	HRE	kidney:	n/a
14	chr13:89815421-89815471	HEK293	kidney:	embryo
15	chr13:89740340-89740390	MCF-7	breast:	n/a
16	chr13:89740340-89740390	HIPEpiC	eye:	n/a
17	chr13:89740340-89740390	K562	blood:	n/a
18	chr13:89815421-89815471	PrEC	prostate:	n/a
19	chr13:89740340-89740390	HCPEpiC	choroid plexus:	n/a
20	chr13:89740340-89740390	RPTEC	kidney:	n/a
21	chr13:89740340-89740390	A549	lung:	n/a
22	chr13:89740340-89740390	HRCEpiC	kidney:	n/a
23	chr13:89815421-89815471	Hela-S3	cervix:	n/a
24	chr13:89740340-89740390	HNPCEpiC	eye:	n/a
25	chr13:89815451-89815501	HCM	heart:	n/a
26	chr13:89815421-89815471	NB4	blood:	n/a
27	chr13:89740340-89740390	MCF10A-Er-Src	breast:	n/a
28	chr13:89815451-89815501	U87	brain:	n/a
29	chr13:89740340-89740390	NH-A	brain:	n/a
30	chr13:89815421-89815471	H1-hESC	embryonic stem cell:	embryo
31	chr13:89815451-89815501	HCF	heart:	n/a
32	chr13:89815451-89815501	GM12892	blood:	n/a
33	chr13:89815451-89815501	MCF10A-Er-Src	breast:	n/a
34	chr13:89815421-89815471	SK-N-SH_RA	brain:	n/a
35	chr13:89740340-89740390	AG10803	skin:	n/a
36	chr13:89815451-89815501	LNCaP	prostate:	n/a
37	chr13:89815421-89815471	HMEC	breast:	n/a
38	chr13:89815451-89815501	Hela-S3	cervix:	n/a
39	chr13:89815451-89815501	HRCEpiC	kidney:	n/a
40	chr13:89815451-89815501	PrEC	prostate:	n/a
41	chr13:89740340-89740390	HAEpiC	amniotic membrane:	n/a
42	chr13:89815421-89815471	SAEC	small airway:	n/a
43	chr13:89815421-89815471	HL-60	blood:	n/a
44	chr13:89740340-89740390	IMR90	lung:	fetal
45	chr13:89815421-89815471	GM12891	blood:	n/a
46	chr13:89815421-89815471	HCT-116	colon:	n/a
47	chr13:89815451-89815501	HepG2	liver:	n/a
48	chr13:89815451-89815501	AG04449	skin:	fetal
49	chr13:89740340-89740390	Jurkat	blood:	n/a
50	chr13:89815421-89815471	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:
2	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:
3	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-21	chr13:89558109-89558584	l_897_chr13:89556162-89558584_testes
2	lnc-SLITRK6-23	chr13:89627871-89627986	l_898_chr13:89627586-89633831_testes
3	lnc-SLITRK6-24	chr13:89815360-89815434	NONHSAT034620
4	lnc-SLITRK6-23	chr13:89627587-89627859	l_898_chr13:89627586-89633831_testes
5	lnc-SLITRK6-23	chr13:89633752-89633831	l_898_chr13:89627586-89633831_testes
6	lnc-SLITRK6-21	chr13:89556163-89556457	l_897_chr13:89556162-89558584_testes
7	lnc-SLITRK6-22	chr13:89630701-89631039	NONHSAT034619
8	lnc-SLITRK6-24	chr13:89811759-89811902	NONHSAT034620

Variant related genes	Relation type
GRPEL2P1	TF binding region
GRPEL2P1	CpG island

Extended variants
information (count: 2697 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2697 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7323385	chr13:89539415-89539416	ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149285278	chr13:89539422-89539423	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs551630407	chr13:89539451-89539452	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570954957	chr13:89539471-89539472	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs371024072	chr13:89539473-89539474	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs144558010	chr13:89539511-89539512	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs77066803	chr13:89539529-89539530	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs568443430	chr13:89539555-89539556	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs535743828	chr13:89539583-89539584	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs180932858	chr13:89539612-89539613	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80341812	chr13:89539642-89539643	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565300935	chr13:89539668-89539669	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574260092	chr13:89539695-89539696	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139371879	chr13:89539716-89539717	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576015289	chr13:89539720-89539721	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543508258	chr13:89539755-89539756	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561499475	chr13:89539776-89539777	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528096141	chr13:89539781-89539782	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528899890	chr13:89539858-89539859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185189070	chr13:89539873-89539874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144166501	chr13:89539965-89539966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374738241	chr13:89540031-89540032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190975055	chr13:89540033-89540034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200386756	chr13:89540061-89540062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72512780	chr13:89540063-89540064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11385208	chr13:89540064-89540065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs66493619	chr13:89540065-89540066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551593090	chr13:89540069-89540070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377314219	chr13:89540098-89540099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146053210	chr13:89540104-89540105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531659981	chr13:89540140-89540141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550268721	chr13:89540141-89540142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568327817	chr13:89540174-89540175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535437490	chr13:89540202-89540203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140049277	chr13:89540206-89540207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142336815	chr13:89540297-89540298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539756953	chr13:89540303-89540304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184066614	chr13:89540355-89540356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189045858	chr13:89540367-89540368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564383066	chr13:89540371-89540372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372953956	chr13:89540372-89540373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536713711	chr13:89540427-89540428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80059477	chr13:89540430-89540431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77409539	chr13:89540440-89540441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567349954	chr13:89540507-89540508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541024568	chr13:89540531-89540532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140501325	chr13:89540576-89540577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536504152	chr13:89540590-89540591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559431823	chr13:89540641-89540642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577966633	chr13:89540654-89540655	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
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
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20841430	CNVD
Wilms tumour	21544195	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89539200-89539800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:89539400-89539600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:89539400-89539800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr13:89539600-89539800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:89539600-89539800	Enhancers	HepG2	liver
6	chr13:89539800-89547600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:89539800-89547600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr13:89539800-89548800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr13:89547600-89548000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr13:89547600-89549000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:89547800-89548400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr13:89548800-89549000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr13:89548800-89549000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr13:89549000-89549200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr13:89557200-89558000	Enhancers	Dnd41	blood
16	chr13:89558000-89560200	Weak transcription	Dnd41	blood
17	chr13:89560200-89562200	Enhancers	Dnd41	blood
18	chr13:89560200-89562600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr13:89561000-89561600	Enhancers	Primary hematopoietic stem cells	blood
20	chr13:89561000-89561600	Enhancers	Brain Hippocampus Middle	brain
21	chr13:89561000-89562000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr13:89561000-89562200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr13:89561200-89561600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr13:89561200-89561600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr13:89561200-89561600	Enhancers	Brain Angular Gyrus	brain
26	chr13:89561200-89561800	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr13:89561200-89561800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr13:89561200-89561800	Enhancers	Adipose Nuclei	Adipose
29	chr13:89561200-89561800	Enhancers	Fetal Muscle Leg	muscle
30	chr13:89561200-89562000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr13:89561200-89562000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr13:89561200-89562000	Enhancers	HMEC	breast
33	chr13:89561200-89562000	Enhancers	NHEK	skin
34	chr13:89561200-89562600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr13:89571000-89571600	Enhancers	Dnd41	blood
36	chr13:89571400-89571600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr13:89571400-89573000	Enhancers	Primary B cells from peripheral blood	blood
38	chr13:89571600-89572400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr13:89571600-89572400	Flanking Active TSS	Dnd41	blood
40	chr13:89571600-89572400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr13:89571600-89572800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr13:89571600-89573200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr13:89571800-89572400	Enhancers	Primary B cells from cord blood	blood
44	chr13:89571800-89572400	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr13:89571800-89572600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr13:89571800-89573000	Enhancers	Primary hematopoietic stem cells	blood
47	chr13:89571800-89573000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr13:89572000-89572600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr13:89572000-89572800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr13:89572000-89572800	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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