Variant report

Variant	nsv1120
Chromosome Location	chr13:92372733-92400616
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	chr13:92400276-92400278	K562	blood:	n/a	n/a
2	ARID3A	chr13:92374503-92374961	HepG2	liver:	n/a	chr13:92374700-92374716 chr13:92374699-92374715
3	ARID3A	chr13:92374274-92374954	K562	blood:	n/a	chr13:92374700-92374716 chr13:92374699-92374715
4	ATF1	chr13:92390219-92390652	K562	blood:	n/a	n/a
5	BACH1	chr13:92400065-92400187	K562	blood:	n/a	n/a
6	BHLHE40	chr13:92374659-92374758	GM12878	blood:	n/a	n/a
7	CEBPB	chr13:92399439-92399813	HepG2	liver:	n/a	chr13:92399616-92399627
8	CEBPB	chr13:92373742-92374059	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr13:92375235-92375349	K562	blood:	n/a	n/a
10	CEBPB	chr13:92399440-92399875	HepG2	liver:	n/a	chr13:92399616-92399627
11	CEBPB	chr13:92374810-92374855	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr13:92392202-92392203	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr13:92392164-92392222	GM12892	blood:	n/a	n/a
14	CTCF	chr13:92374700-92374850	HEK293	kidney:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
15	CTCF	chr13:92388017-92388058	GM13976	blood:	n/a	n/a
16	CTCF	chr13:92374600-92374750	GM12864	blood:	n/a	n/a
17	CTCF	chr13:92374660-92374810	HEEpiC	esophagus:	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	chr13:92374760-92374910	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr13:92375006-92375050	GM12878	blood:	n/a	n/a
20	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
21	CTCF	chr13:92374660-92374810	GM12873	blood:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
22	CTCF	chr13:92374680-92374830	HMEC	breast:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
23	CTCF	chr13:92374640-92374790	HPAF	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
24	CTCF	chr13:92374567-92374867	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
25	CTCF	chr13:92392100-92392250	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr13:92374680-92374830	NHLF	lung:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
27	CTCF	chr13:92392100-92392245	HepG2	liver:	n/a	n/a
28	CTCF	chr13:92374720-92374870	GM12872	blood:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
29	CTCF	chr13:92374326-92375136	A549	lung:	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	chr13:92374740-92374890	HA-sp	spinal cord:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374741-92374751 chr13:92374740-92374753
31	CTCF	chr13:92374680-92374830	GM12872	blood:	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	chr13:92392100-92392250	BE2_C	brain:	n/a	n/a
33	CTCF	chr13:92392080-92392230	HMEC	breast:	n/a	n/a
34	CTCF	chr13:92374700-92374850	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
35	CTCF	chr13:92392021-92392316	GM12878	blood:	n/a	n/a
36	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
37	CTCF	chr13:92392060-92392210	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr13:92391980-92392130	GM12866	blood:	n/a	n/a
39	CTCF	chr13:92374674-92374849	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
40	CTCF	chr13:92374714-92374864	Gliobla	brain:	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	chr13:92374538-92374925	A549	lung:	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	chr13:92374664-92374791	SK-N-SH_RA	brain:	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	chr13:92374640-92374790	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
44	CTCF	chr13:92374645-92374870	K562	blood:	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	chr13:92374700-92374850	Hela-S3	cervix:	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	chr13:92374720-92374870	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
47	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
48	CTCF	chr13:92374660-92374810	HCPEpiC	choroid plexus:	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	chr13:92374660-92374810	AG04449	skin:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756
50	CTCF	chr13:92374650-92374853	GM13977	blood:	n/a	chr13:92374740-92374753 chr13:92374744-92374753 chr13:92374733-92374754 chr13:92374739-92374755 chr13:92374741-92374751 chr13:92374740-92374753 chr13:92374738-92374756

No.	Distal block	Cell Line	Cell type
1	chr13:91999817..92002695-chr13:92390327..92393222,2	K562	blood:
2	chr13:92145807..92146368-chr13:92374222..92374906,2	MCF-7	breast:
3	chr13:92042645..92045242-chr13:92380506..92382090,2	K562	blood:
4	chr13:92387450..92389027-chr13:92396587..92398169,2	K562	blood:
5	chr13:92359085..92361584-chr13:92399636..92402308,3	K562	blood:
6	chr13:92376837..92379640-chr13:92380146..92383105,2	K562	blood:
7	chr13:92008256..92010781-chr13:92387538..92390308,3	K562	blood:
8	chr13:92027062..92028258-chr13:92373843..92375196,5	K562	blood:
9	chr13:91999942..92002142-chr13:92375308..92377131,2	K562	blood:
10	chr13:92354089..92355677-chr13:92374923..92376829,2	K562	blood:
11	chr13:92373425..92375366-chr13:92378458..92381113,2	K562	blood:
12	chr13:92367826..92370130-chr13:92386601..92389593,3	K562	blood:
13	chr13:92009230..92011038-chr13:92380409..92382263,2	K562	blood:
14	chr13:92360673..92364481-chr13:92372533..92375475,4	K562	blood:
15	chr13:92348342..92351314-chr13:92379204..92381548,2	K562	blood:
16	chr13:91999828..92001377-chr13:92382768..92385377,2	K562	blood:
17	chr13:92383340..92385444-chr13:92386472..92389094,2	K562	blood:
18	chr13:92392822..92394386-chr13:92398507..92400283,2	K562	blood:
19	chr13:92367060..92370177-chr13:92371319..92374690,3	K562	blood:
20	chr13:92357827..92359421-chr13:92380586..92382963,2	K562	blood:
21	chr13:92007816..92009567-chr13:92393385..92396123,2	K562	blood:
22	chr13:92397745..92400053-chr13:92406336..92408253,2	K562	blood:
23	chr13:92387450..92389027-chr13:92396587..92398169,2	K562	blood:
24	chr13:92360463..92365110-chr13:92381034..92383845,4	K562	blood:
25	chr13:92011474..92014177-chr13:92380431..92383913,3	K562	blood:
26	chr13:91998144..92000797-chr13:92374828..92377149,2	K562	blood:
27	chr13:92373425..92375366-chr13:92378458..92381113,2	K562	blood:
28	chr13:91999426..92001246-chr13:92399597..92401347,2	K562	blood:
29	chr13:92058657..92059487-chr13:92374237..92374819,3	K562	blood:
30	chr13:92035701..92038096-chr13:92377993..92380775,2	K562	blood:
31	chr13:92383340..92385444-chr13:92386472..92389094,2	K562	blood:
32	chr13:91998613..92001393-chr13:92380186..92381760,2	K562	blood:
33	chr13:92373425..92376010-chr13:92378943..92381113,2	K562	blood:
34	chr13:92363299..92365110-chr13:92382345..92384889,2	K562	blood:
35	chr13:92011581..92014280-chr13:92377653..92379925,3	K562	blood:
36	chr13:92033406..92034232-chr13:92374271..92374898,2	MCF-7	breast:
37	chr13:92373425..92376010-chr13:92378943..92381113,2	K562	blood:
38	chr13:92011474..92015304-chr13:92379938..92384751,4	K562	blood:
39	chr13:92392822..92394386-chr13:92398507..92400283,2	K562	blood:

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

Extended variants
information (count: 1054 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186126407	chr13:92372733-92372734	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551589293	chr13:92372745-92372746	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs571574857	chr13:92372792-92372793	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374247842	chr13:92372858-92372859	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs537294979	chr13:92372988-92372989	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs147778795	chr13:92373034-92373035	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs141104736	chr13:92373051-92373052	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372833939	chr13:92373066-92373067	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs570333169	chr13:92373100-92373101	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs373397290	chr13:92373126-92373127	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs368034203	chr13:92373142-92373143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3904388	chr13:92373181-92373182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146967272	chr13:92373193-92373194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371562031	chr13:92373197-92373198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143670938	chr13:92373221-92373222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568034404	chr13:92373305-92373306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113601597	chr13:92373311-92373312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377221755	chr13:92373318-92373319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544477565	chr13:92373354-92373355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562962040	chr13:92373366-92373367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200624780	chr13:92373371-92373372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528908777	chr13:92373391-92373392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548958902	chr13:92373395-92373396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201467210	chr13:92373397-92373398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112451550	chr13:92373412-92373413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528147230	chr13:92373428-92373429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143137549	chr13:92373453-92373454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551603743	chr13:92373457-92373458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571438857	chr13:92373490-92373491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534180278	chr13:92373513-92373514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148237950	chr13:92373545-92373546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369045391	chr13:92373575-92373576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71427526	chr13:92373582-92373583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371254398	chr13:92373585-92373586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141373554	chr13:92373611-92373612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536296619	chr13:92373640-92373641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553322832	chr13:92373643-92373644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557269866	chr13:92373653-92373654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573268544	chr13:92373661-92373662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375862793	chr13:92373668-92373669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538702763	chr13:92373674-92373675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192097472	chr13:92373714-92373715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546794274	chr13:92373721-92373722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552627484	chr13:92373740-92373741	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs533623137	chr13:92373747-92373748	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs562825767	chr13:92373760-92373761	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs375562627	chr13:92373834-92373835	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs544376733	chr13:92373899-92373900	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561470783	chr13:92373907-92373908	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs184085743	chr13:92373947-92373948	Weak transcription Enhancers	TF binding 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:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92370800-92375800	Enhancers	Hela-S3	cervix
2	chr13:92371800-92376600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr13:92373800-92374600	Enhancers	Fetal Muscle Leg	muscle
4	chr13:92374000-92374400	Enhancers	Fetal Heart	heart
5	chr13:92374400-92377000	Weak transcription	Fetal Heart	heart
6	chr13:92375800-92377200	Weak transcription	Hela-S3	cervix
7	chr13:92376600-92379400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr13:92376800-92377400	Enhancers	Ovary	ovary
9	chr13:92376800-92377800	Enhancers	Fetal Intestine Large	intestine
10	chr13:92377000-92378600	Enhancers	Fetal Heart	heart
11	chr13:92377200-92377600	Enhancers	Fetal Lung	lung
12	chr13:92377200-92377600	Enhancers	Hela-S3	cervix
13	chr13:92377400-92378200	Enhancers	Fetal Intestine Small	intestine
14	chr13:92377600-92378000	Weak transcription	Ovary	ovary
15	chr13:92377600-92382400	Weak transcription	Hela-S3	cervix
16	chr13:92377800-92378200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr13:92377800-92378800	Weak transcription	Fetal Intestine Large	intestine
18	chr13:92378800-92379200	Enhancers	Fetal Intestine Large	intestine
19	chr13:92379000-92379200	Enhancers	Ovary	ovary
20	chr13:92382400-92383000	Strong transcription	Hela-S3	cervix
21	chr13:92383000-92419400	Weak transcription	Hela-S3	cervix
22	chr13:92392200-92393400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr13:92392200-92393400	Enhancers	Brain Germinal Matrix	brain
24	chr13:92393400-92399400	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr13:92394200-92395000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:92396200-92396600	Enhancers	Fetal Heart	heart
27	chr13:92396600-92397000	Flanking Active TSS	Fetal Heart	heart
28	chr13:92397000-92398800	Enhancers	Fetal Heart	heart
29	chr13:92397800-92398600	Enhancers	Fetal Intestine Small	intestine
30	chr13:92398800-92399600	Weak transcription	Fetal Heart	heart
31	chr13:92399400-92400600	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr13:92399600-92399800	Enhancers	Fetal Heart	heart
33	chr13:92399600-92399800	Enhancers	Left Ventricle	heart
34	chr13:92399600-92399800	Enhancers	Right Atrium	heart
35	chr13:92399600-92400000	Enhancers	Brain Hippocampus Middle	brain
36	chr13:92399600-92400200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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