Variant report

Variant	nsv462212
Chromosome Location	chr5:75388834-75534570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1297)
CpG islands
(count:673)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:75517243-75517452	K562	blood:	n/a	n/a
2	ATF1	chr5:75442283-75442385	K562	blood:	n/a	n/a
3	ATF1	chr5:75458345-75458529	K562	blood:	n/a	n/a
4	ATF1	chr5:75515637-75515837	K562	blood:	n/a	n/a
5	ATF1	chr5:75471623-75472170	K562	blood:	n/a	n/a
6	ATF1	chr5:75476928-75477230	K562	blood:	n/a	n/a
7	ATF2	chr5:75474597-75475178	GM12878	blood:	n/a	n/a
8	ATF2	chr5:75394969-75395455	GM12878	blood:	n/a	n/a
9	ATF2	chr5:75394893-75395805	GM12878	blood:	n/a	n/a
10	ATF2	chr5:75471604-75472348	GM12878	blood:	n/a	n/a
11	ATF2	chr5:75474650-75475133	GM12878	blood:	n/a	n/a
12	ATF2	chr5:75483142-75483633	GM12878	blood:	n/a	n/a
13	ATF2	chr5:75476882-75477667	GM12878	blood:	n/a	n/a
14	ATF2	chr5:75476912-75477609	GM12878	blood:	n/a	n/a
15	ATF2	chr5:75471452-75472442	GM12878	blood:	n/a	n/a
16	ATF3	chr5:75471599-75472016	K562	blood:	n/a	n/a
17	BATF	chr5:75476907-75477562	GM12878	blood:	n/a	n/a
18	BATF	chr5:75395097-75395564	GM12878	blood:	n/a	n/a
19	BATF	chr5:75474748-75475148	GM12878	blood:	n/a	n/a
20	BATF	chr5:75476903-75477253	GM12878	blood:	n/a	n/a
21	BATF	chr5:75471890-75472287	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:75474738-75475112	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:75440843-75440979	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr5:75476940-75477332	GM12878	blood:	n/a	n/a
25	BCL3	chr5:75476943-75477631	GM12878	blood:	n/a	n/a
26	BCL3	chr5:75473860-75474199	GM12878	blood:	n/a	n/a
27	BCL3	chr5:75471555-75472304	GM12878	blood:	n/a	n/a
28	BCL3	chr5:75474685-75475133	GM12878	blood:	n/a	n/a
29	BCLAF1	chr5:75476931-75477519	GM12878	blood:	n/a	n/a
30	BCLAF1	chr5:75394943-75395528	GM12878	blood:	n/a	n/a
31	BCLAF1	chr5:75470838-75471335	GM12878	blood:	n/a	n/a
32	BCLAF1	chr5:75471604-75472393	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:75471965-75472226	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:75470933-75471235	GM12878	blood:	n/a	n/a
35	BHLHE40	chr5:75441876-75442076	K562	blood:	n/a	n/a
36	BHLHE40	chr5:75471619-75472026	K562	blood:	n/a	n/a
37	BHLHE40	chr5:75476870-75477240	K562	blood:	n/a	n/a
38	BHLHE40	chr5:75515244-75515285	GM12878	blood:	n/a	n/a
39	CBX3	chr5:75476823-75477541	K562	blood:	n/a	n/a
40	CBX3	chr5:75505170-75505419	K562	blood:	n/a	n/a
41	CBX3	chr5:75471552-75472056	K562	blood:	n/a	n/a
42	CCNT2	chr5:75471729-75471951	K562	blood:	n/a	chr5:75471940-75471949
43	CCNT2	chr5:75530726-75530914	K562	blood:	n/a	n/a
44	CCNT2	chr5:75476951-75477181	K562	blood:	n/a	n/a
45	CEBPB	chr5:75439719-75440089	IMR90	lung:	n/a	chr5:75439901-75439912
46	CEBPB	chr5:75394589-75394856	HepG2	liver:	n/a	chr5:75394674-75394685
47	CEBPB	chr5:75408204-75408239	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:75476639-75476847	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:75476703-75477146	MCF-7	breast:	n/a	n/a
50	CEBPB	chr5:75476650-75477197	MCF-7	breast:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75470039-75470089	PrEC	prostate:	n/a
2	chr5:75469826-75469876	PFSK-1	brain:	n/a
3	chr5:75470039-75470089	PrEC	prostate:	n/a
4	chr5:75469826-75469876	PFSK-1	brain:	n/a
5	chr5:75470039-75470089	ovcar-3	ovarian:	n/a
6	chr5:75470039-75470089	Hepatocyte	liver:	n/a
7	chr5:75469969-75470019	GM06990	blood:	n/a
8	chr5:75472143-75472193	GM06990	blood:	n/a
9	chr5:75469826-75469876	NB4	blood:	n/a
10	chr5:75469826-75469876	BJ	skin:	n/a
11	chr5:75469969-75470019	U87	brain:	n/a
12	chr5:75469904-75469954	NT2-D1	testis:	n/a
13	chr5:75469826-75469876	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:75471166-75471216	Caco-2	colon:	n/a
15	chr5:75472143-75472193	HepG2	liver:	n/a
16	chr5:75465603-75465653	AG09319	gingival:	n/a
17	chr5:75465603-75465653	HCM	heart:	n/a
18	chr5:75473201-75473251	HCF	heart:	n/a
19	chr5:75410147-75410197	HIPEpiC	eye:	n/a
20	chr5:75465603-75465653	SKMC	muscle:	n/a
21	chr5:75469969-75470019	HL-60	blood:	n/a
22	chr5:75524056-75524106	HCT-116	colon:	n/a
23	chr5:75470039-75470089	SAEC	small airway:	n/a
24	chr5:75524056-75524106	BE2_C	brain:	n/a
25	chr5:75410147-75410197	AoSMC	blood vessel:	n/a
26	chr5:75464408-75464458	AG10803	skin:	n/a
27	chr5:75472143-75472193	Hepatocyte	liver:	n/a
28	chr5:75473201-75473251	HL-60	blood:	n/a
29	chr5:75410147-75410197	HEEpiC	esophagus:	n/a
30	chr5:75473201-75473251	Hela-S3	cervix:	n/a
31	chr5:75473201-75473251	SK-N-SH_RA	brain:	n/a
32	chr5:75465603-75465653	NHDF-neo	bronchial:	n/a
33	chr5:75469969-75470019	HRE	kidney:	n/a
34	chr5:75472143-75472193	H1-hESC	embryonic stem cell:	embryo
35	chr5:75469904-75469954	HRCEpiC	kidney:	n/a
36	chr5:75473201-75473251	CMK	blood:	n/a
37	chr5:75471166-75471216	NB4	blood:	n/a
38	chr5:75469969-75470019	ProgFib	skin:	n/a
39	chr5:75472143-75472193	SAEC	small airway:	n/a
40	chr5:75524056-75524106	T-47D	breast:	n/a
41	chr5:75469904-75469954	NHBE	bronchial:	n/a
42	chr5:75524056-75524106	HCM	heart:	n/a
43	chr5:75473201-75473251	IMR90	lung:	fetal
44	chr5:75464408-75464458	ProgFib	skin:	n/a
45	chr5:75465603-75465653	SK-N-SH_RA	brain:	n/a
46	chr5:75471166-75471216	AG04450	lung:	fetal
47	chr5:75469969-75470019	ovcar-3	ovarian:	n/a
48	chr5:75469969-75470019	LNCaP	prostate:	n/a
49	chr5:75472143-75472193	GM19239	blood:	n/a
50	chr5:75470039-75470089	GM06990	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75370258..75370917-chr5:75470691..75471438,2	MCF-7	breast:
2	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
3	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
4	chr5:75011937..75013471-chr5:75474552..75477211,2	MCF-7	breast:
5	chr5:75422773..75425695-chr5:75433984..75435838,2	K562	blood:
6	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
7	chr4:144295435..144296093-chr5:75459165..75460000,2	MCF-7	breast:
8	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
9	chr5:75470625..75471456-chr5:75551799..75552684,5	MCF-7	breast:
10	chr5:75369710..75371593-chr5:75472300..75473889,2	K562	blood:
11	chr5:75518200..75520510-chr5:75524409..75526255,2	K562	blood:
12	chr5:75031130..75031721-chr5:75470748..75471418,2	MCF-7	breast:
13	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
14	chr5:75484578..75486755-chr5:75492728..75495660,2	K562	blood:
15	chr5:75182130..75182669-chr5:75470688..75471450,3	MCF-7	breast:
16	chr5:75469938..75472744-chr5:75476639..75478302,2	K562	blood:
17	chr2:175960283..175962736-chr5:75428852..75431360,2	MCF-7	breast:
18	chr5:75030911..75031730-chr5:75470555..75471416,3	MCF-7	breast:
19	chr5:75511321..75513183-chr5:75515341..75518158,2	MCF-7	breast:
20	chr5:75370002..75370997-chr5:75470399..75471572,8	MCF-7	breast:
21	chr5:75520569..75523367-chr5:75540398..75542001,2	K562	blood:
22	chr5:75441859..75445534-chr5:75469171..75472141,3	K562	blood:
23	chr5:75435891..75438461-chr5:75439201..75442019,2	K562	blood:
24	chr2:77243462..77244011-chr5:75510913..75511675,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000251668	TF binding region
ENSG00000254893	TF binding region
RNA5SP186	TF binding region
ENSG00000251668	CpG island
ENSG00000254893	CpG island
RNA5SP186	CpG island
ENSG00000254893	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000249777	chromatin interactions

Extended variants
information (count: 3442 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3442 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150355541	chr5:75389395-75389396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs189091431	chr5:75389402-75389403	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569882628	chr5:75389475-75389476	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs553132174	chr5:75391736-75391737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs529026949	chr5:75391770-75391771	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs190780960	chr5:75391798-75391799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs559757008	chr5:75391822-75391823	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs34203814	chr5:75391852-75391853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs528565247	chr5:75391872-75391873	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs187288504	chr5:75393814-75393815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73764008	chr5:75393880-75393881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs113311670	chr5:75393911-75393912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560580945	chr5:75393932-75393933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150199446	chr5:75393950-75393951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368863109	chr5:75393977-75393978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs193050592	chr5:75394055-75394056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185221940	chr5:75394110-75394111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558275622	chr5:75394132-75394133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188884622	chr5:75394160-75394161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550225307	chr5:75394171-75394172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567274165	chr5:75394210-75394211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193103155	chr5:75394243-75394244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546567686	chr5:75394281-75394282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183775416	chr5:75394308-75394309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538915497	chr5:75394317-75394318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34204558	chr5:75394336-75394337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558822429	chr5:75394342-75394343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573474839	chr5:75394344-75394345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575476036	chr5:75394345-75394346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538365020	chr5:75394360-75394361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573885817	chr5:75394375-75394376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138704068	chr5:75394379-75394380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149437615	chr5:75394459-75394460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540308924	chr5:75394488-75394489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544159172	chr5:75394519-75394520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554885505	chr5:75394529-75394530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376629635	chr5:75394566-75394567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12110148	chr5:75394645-75394646	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546069861	chr5:75394693-75394694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562756232	chr5:75394697-75394698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188449466	chr5:75394720-75394721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144837321	chr5:75394728-75394729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139726274	chr5:75394782-75394783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375339180	chr5:75394814-75394815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181211340	chr5:75394846-75394847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17650698	chr5:75394901-75394902	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs7700761	chr5:75394915-75394916	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs532479938	chr5:75394968-75394969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532463584	chr5:75394971-75394972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117124071	chr5:75395030-75395031	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75393800-75395200	Enhancers	GM12878-XiMat	blood
2	chr5:75395000-75395600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr5:75395000-75395800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr5:75395000-75396400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
5	chr5:75395200-75395600	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr5:75395200-75395800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr5:75395200-75395800	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr5:75395200-75395800	Flanking Active TSS	GM12878-XiMat	blood
9	chr5:75395200-75396000	Enhancers	Primary T cells from cord blood	blood
10	chr5:75395200-75396000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr5:75395400-75395800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr5:75395400-75396000	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr5:75395400-75396000	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr5:75395800-75396400	Enhancers	GM12878-XiMat	blood
15	chr5:75400000-75401800	Enhancers	Stomach Mucosa	stomach
16	chr5:75400200-75401200	Enhancers	Duodenum Mucosa	Duodenum
17	chr5:75401800-75402200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:75401800-75406600	Weak transcription	Stomach Mucosa	stomach
19	chr5:75406600-75409400	Enhancers	Stomach Mucosa	stomach
20	chr5:75407200-75407800	Enhancers	HUVEC	blood vessel
21	chr5:75407400-75407600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:75407600-75407800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:75407600-75407800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr5:75407800-75409800	Weak transcription	HUVEC	blood vessel
25	chr5:75408200-75408400	Enhancers	Left Ventricle	heart
26	chr5:75408200-75408400	Enhancers	Lung	lung
27	chr5:75408200-75408400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr5:75408200-75409800	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr5:75408200-75410600	Enhancers	Gastric	stomach
30	chr5:75408400-75409400	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr5:75408400-75409800	Weak transcription	Lung	lung
32	chr5:75408600-75409800	Weak transcription	Left Ventricle	heart
33	chr5:75409200-75409800	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr5:75409400-75409800	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr5:75409400-75410000	Flanking Active TSS	Stomach Mucosa	stomach
36	chr5:75409400-75411400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr5:75409400-75412200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:75409600-75410200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:75409600-75410400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:75409600-75410600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr5:75409600-75410600	Enhancers	Duodenum Mucosa	Duodenum
42	chr5:75409800-75410000	Enhancers	Brain Anterior Caudate	brain
43	chr5:75409800-75410000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
44	chr5:75409800-75410000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
45	chr5:75409800-75410000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
46	chr5:75409800-75410200	Enhancers	Adipose Nuclei	Adipose
47	chr5:75409800-75410200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr5:75409800-75410200	Enhancers	Pancreas	Pancrea
49	chr5:75409800-75410400	Enhancers	Colonic Mucosa	Colon
50	chr5:75409800-75410400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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