Variant report

Variant	nsv562718
Chromosome Location	chr13:92366257-92399564
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	ARID3A	chr13:92374503-92374961	HepG2	liver:	n/a	chr13:92374700-92374716 chr13:92374699-92374715
2	ARID3A	chr13:92374274-92374954	K562	blood:	n/a	chr13:92374700-92374716 chr13:92374699-92374715
3	ATF1	chr13:92368532-92369138	K562	blood:	n/a	n/a
4	ATF1	chr13:92390219-92390652	K562	blood:	n/a	n/a
5	BACH1	chr13:92368006-92368076	K562	blood:	n/a	n/a
6	BACH1	chr13:92371342-92371659	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr13:92374659-92374758	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:92369254-92369334	K562	blood:	n/a	n/a
9	CEBPB	chr13:92375235-92375349	K562	blood:	n/a	n/a
10	CEBPB	chr13:92399439-92399813	HepG2	liver:	n/a	chr13:92399616-92399627
11	CEBPB	chr13:92371334-92371680	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr13:92399440-92399875	HepG2	liver:	n/a	chr13:92399616-92399627
13	CEBPB	chr13:92374810-92374855	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr13:92373742-92374059	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr13:92392202-92392203	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr13:92374640-92374790	GM12864	blood:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
17	CTCF	chr13:92374640-92374790	HCM	heart:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
18	CTCF	chr13:92374720-92374870	GM12871	blood:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
19	CTCF	chr13:92374520-92374874	HCT-116	colon:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
20	CTCF	chr13:92392134-92392252	MCF-7	breast:	n/a	n/a
21	CTCF	chr13:92392134-92392208	GM19239	blood:	n/a	n/a
22	CTCF	chr13:92392150-92392210	GM12878	blood:	n/a	n/a
23	CTCF	chr13:92374660-92374810	GM12866	blood:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
24	CTCF	chr13:92374555-92374964	IMR90	lung:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
25	CTCF	chr13:92374080-92375101	SK-N-SH	brain:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
26	CTCF	chr13:92392129-92392266	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr13:92374220-92374370	K562	blood:	n/a	n/a
28	CTCF	chr13:92374520-92374670	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:92374698-92374809	GM13976	blood:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
30	CTCF	chr13:92374556-92374900	MCF-7	breast:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
31	CTCF	chr13:92374640-92374790	HepG2	liver:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
32	CTCF	chr13:92374640-92374790	RPTEC	kidney:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
33	CTCF	chr13:92374634-92374820	Lung_OC	lung:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
34	CTCF	chr13:92392151-92392166	Medullo	brain:	n/a	n/a
35	CTCF	chr13:92374640-92374790	HFF-Myc	foreskin:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
36	CTCF	chr13:92392120-92392270	HRE	kidney:	n/a	n/a
37	CTCF	chr13:92388017-92388058	GM13976	blood:	n/a	n/a
38	CTCF	chr13:92374640-92374790	HAc	cerebellar:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
39	CTCF	chr13:92392160-92392310	HEK293	kidney:	n/a	n/a
40	CTCF	chr13:92374620-92374770	BJ	skin:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
41	CTCF	chr13:92374680-92374830	HCT-116	colon:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
42	CTCF	chr13:92374680-92374830	SAEC	small airway:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
43	CTCF	chr13:92374280-92374430	GM12873	blood:	n/a	n/a
44	CTCF	chr13:92374700-92374850	AG04450	lung:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
45	CTCF	chr13:92374652-92374846	LNCaP	prostate:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
46	CTCF	chr13:92392200-92392350	HMEC	breast:	n/a	n/a
47	CTCF	chr13:92392049-92392266	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr13:92374680-92374830	AoAF	blood vessel:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
49	CTCF	chr13:92381223-92381227	K562	blood:	n/a	n/a
50	CTCF	chr13:92375000-92375150	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:92011474..92014177-chr13:92380431..92383913,3	K562	blood:
2	chr13:92373425..92376010-chr13:92378943..92381113,2	K562	blood:
3	chr13:92387450..92389027-chr13:92396587..92398169,2	K562	blood:
4	chr13:92354089..92355677-chr13:92374923..92376829,2	K562	blood:
5	chr13:92011581..92014280-chr13:92377653..92379925,3	K562	blood:
6	chr13:92392822..92394386-chr13:92398507..92400283,2	K562	blood:
7	chr13:91998613..92001393-chr13:92380186..92381760,2	K562	blood:
8	chr13:92383340..92385444-chr13:92386472..92389094,2	K562	blood:
9	chr13:92397745..92400053-chr13:92406336..92408253,2	K562	blood:
10	chr13:92373425..92375366-chr13:92378458..92381113,2	K562	blood:
11	chr13:92008256..92010781-chr13:92387538..92390308,3	K562	blood:
12	chr13:91999817..92002695-chr13:92390327..92393222,2	K562	blood:
13	chr13:92357827..92359421-chr13:92380586..92382963,2	K562	blood:
14	chr13:91999828..92001377-chr13:92382768..92385377,2	K562	blood:
15	chr13:92367060..92370177-chr13:92371319..92374690,3	K562	blood:
16	chr13:92360673..92364481-chr13:92372533..92375475,4	K562	blood:
17	chr13:92376837..92379640-chr13:92380146..92383105,2	K562	blood:
18	chr13:92035701..92038096-chr13:92377993..92380775,2	K562	blood:
19	chr13:92058657..92059487-chr13:92374237..92374819,3	K562	blood:
20	chr13:92027062..92028258-chr13:92373843..92375196,5	K562	blood:
21	chr13:92373425..92376010-chr13:92378943..92381113,2	K562	blood:
22	chr13:92033406..92034232-chr13:92374271..92374898,2	MCF-7	breast:
23	chr13:92363299..92365110-chr13:92382345..92384889,2	K562	blood:
24	chr13:91999695..92001693-chr13:92369101..92370958,3	K562	blood:
25	chr13:92373425..92375366-chr13:92378458..92381113,2	K562	blood:
26	chr13:91998144..92000797-chr13:92374828..92377149,2	K562	blood:
27	chr13:92009230..92011038-chr13:92380409..92382263,2	K562	blood:
28	chr13:92011474..92015304-chr13:92379938..92384751,4	K562	blood:
29	chr13:92348342..92351314-chr13:92379204..92381548,2	K562	blood:
30	chr13:92383340..92385444-chr13:92386472..92389094,2	K562	blood:
31	chr13:92367826..92370130-chr13:92386601..92389593,3	K562	blood:
32	chr13:92008998..92011983-chr13:92367729..92370311,3	K562	blood:
33	chr13:92367060..92370177-chr13:92371319..92374690,3	K562	blood:
34	chr13:92145807..92146368-chr13:92374222..92374906,2	MCF-7	breast:
35	chr13:91999809..92002050-chr13:92364796..92366548,2	K562	blood:
36	chr13:92392822..92394386-chr13:92398507..92400283,2	K562	blood:
37	chr13:91999942..92002142-chr13:92375308..92377131,2	K562	blood:
38	chr13:92007816..92009567-chr13:92393385..92396123,2	K562	blood:
39	chr13:92387450..92389027-chr13:92396587..92398169,2	K562	blood:
40	chr13:92042645..92045242-chr13:92380506..92382090,2	K562	blood:
41	chr13:92367826..92370130-chr13:92386601..92389593,3	K562	blood:
42	chr13:92360463..92365110-chr13:92381034..92383845,4	K562	blood:

Variant related genes	Relation type
GPC5	TF binding region
ENSG00000215417	chromatin interactions
ENSG00000179399	chromatin interactions

Extended variants
information (count: 1221 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs460929	chr13:92366257-92366258	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189697393	chr13:92366318-92366319	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569012939	chr13:92366366-92366367	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531240027	chr13:92366389-92366390	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs550834906	chr13:92366418-92366419	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373600091	chr13:92366441-92366442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569327902	chr13:92366449-92366450	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs376426034	chr13:92366455-92366456	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs367699568	chr13:92366548-92366549	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181296483	chr13:92366804-92366805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545127325	chr13:92366820-92366821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113520757	chr13:92366822-92366823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565496735	chr13:92366837-92366838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530979901	chr13:92366852-92366853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576090432	chr13:92366856-92366857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568710460	chr13:92366860-92366861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369782059	chr13:92366882-92366883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561292942	chr13:92366905-92366906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376695700	chr13:92366922-92366923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117764523	chr13:92366940-92366941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534206172	chr13:92366941-92366942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530317945	chr13:92366970-92366971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554538594	chr13:92367004-92367005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577502105	chr13:92367023-92367024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541519832	chr13:92367028-92367029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553466404	chr13:92367096-92367097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528209447	chr13:92367109-92367110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368775207	chr13:92367113-92367114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549238	chr13:92367132-92367133	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370500353	chr13:92367156-92367157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs516860	chr13:92367183-92367184	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs73607091	chr13:92367197-92367198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115806110	chr13:92367205-92367206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548332	chr13:92367221-92367222	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs536513106	chr13:92367266-92367267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553337420	chr13:92367267-92367268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573127015	chr13:92367269-92367270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545499718	chr13:92367302-92367303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576305873	chr13:92367383-92367384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575313923	chr13:92367388-92367389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544442929	chr13:92367425-92367426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561104463	chr13:92367431-92367432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76032035	chr13:92367471-92367472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574795255	chr13:92367475-92367476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540497244	chr13:92367515-92367516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76122008	chr13:92367518-92367519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528106477	chr13:92367581-92367582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373515281	chr13:92369126-92369127	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376214830	chr13:92369132-92369133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs373185159	chr13:92369212-92369213	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92366800-92367400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr13:92367000-92367200	Enhancers	Brain Substantia Nigra	brain
3	chr13:92367000-92367400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr13:92367200-92367600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:92369600-92369800	Enhancers	Hela-S3	cervix
6	chr13:92369800-92370800	Weak transcription	Hela-S3	cervix
7	chr13:92370800-92371600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr13:92370800-92372000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr13:92370800-92375800	Enhancers	Hela-S3	cervix
10	chr13:92371000-92371800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:92371000-92371800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr13:92371200-92371600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr13:92371400-92371800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr13:92371400-92371800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr13:92371800-92376600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr13:92373800-92374600	Enhancers	Fetal Muscle Leg	muscle
17	chr13:92374000-92374400	Enhancers	Fetal Heart	heart
18	chr13:92374400-92377000	Weak transcription	Fetal Heart	heart
19	chr13:92375800-92377200	Weak transcription	Hela-S3	cervix
20	chr13:92376600-92379400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr13:92376800-92377400	Enhancers	Ovary	ovary
22	chr13:92376800-92377800	Enhancers	Fetal Intestine Large	intestine
23	chr13:92377000-92378600	Enhancers	Fetal Heart	heart
24	chr13:92377200-92377600	Enhancers	Fetal Lung	lung
25	chr13:92377200-92377600	Enhancers	Hela-S3	cervix
26	chr13:92377400-92378200	Enhancers	Fetal Intestine Small	intestine
27	chr13:92377600-92378000	Weak transcription	Ovary	ovary
28	chr13:92377600-92382400	Weak transcription	Hela-S3	cervix
29	chr13:92377800-92378200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr13:92377800-92378800	Weak transcription	Fetal Intestine Large	intestine
31	chr13:92378800-92379200	Enhancers	Fetal Intestine Large	intestine
32	chr13:92379000-92379200	Enhancers	Ovary	ovary
33	chr13:92382400-92383000	Strong transcription	Hela-S3	cervix
34	chr13:92383000-92419400	Weak transcription	Hela-S3	cervix
35	chr13:92392200-92393400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr13:92392200-92393400	Enhancers	Brain Germinal Matrix	brain
37	chr13:92393400-92399400	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr13:92394200-92395000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:92396200-92396600	Enhancers	Fetal Heart	heart
40	chr13:92396600-92397000	Flanking Active TSS	Fetal Heart	heart
41	chr13:92397000-92398800	Enhancers	Fetal Heart	heart
42	chr13:92397800-92398600	Enhancers	Fetal Intestine Small	intestine
43	chr13:92398800-92399600	Weak transcription	Fetal Heart	heart
44	chr13:92399400-92400600	Enhancers	Cortex derived primary cultured neurospheres	brain

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