Variant report

Variant	nsv462331
Chromosome Location	chr5:103408356-103472789
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	chr5:103424586-103425489	K562	blood:	n/a	n/a
2	ATF1	chr5:103424670-103425482	K562	blood:	n/a	n/a
3	ATF1	chr5:103427458-103427492	K562	blood:	n/a	n/a
4	ATF3	chr5:103425143-103425446	K562	blood:	n/a	n/a
5	BACH1	chr5:103425247-103425428	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:103424849-103425597	K562	blood:	n/a	n/a
7	BACH1	chr5:103420138-103420206	K562	blood:	n/a	n/a
8	BATF	chr5:103425096-103425463	GM12878	blood:	n/a	chr5:103425282-103425293
9	BATF	chr5:103425050-103425493	GM12878	blood:	n/a	chr5:103425282-103425293
10	BCL11A	chr5:103425108-103425491	GM12878	blood:	n/a	chr5:103425281-103425290 chr5:103425282-103425291
11	BCL11A	chr5:103425087-103425461	GM12878	blood:	n/a	chr5:103425281-103425290 chr5:103425282-103425291
12	BHLHE40	chr5:103424858-103425183	K562	blood:	n/a	n/a
13	CBX3	chr5:103424562-103425521	K562	blood:	n/a	n/a
14	CBX3	chr5:103424834-103425657	HCT-116	colon:	n/a	n/a
15	CBX3	chr5:103469878-103470276	K562	blood:	n/a	n/a
16	CBX3	chr5:103440319-103440817	K562	blood:	n/a	n/a
17	CCNT2	chr5:103424875-103425443	K562	blood:	n/a	n/a
18	CEBPB	chr5:103464069-103464443	HepG2	liver:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
19	CEBPB	chr5:103426969-103427287	HepG2	liver:	n/a	chr5:103427132-103427145 chr5:103427134-103427143 chr5:103427134-103427143 chr5:103427132-103427145 chr5:103427132-103427145 chr5:103427132-103427143 chr5:103427142-103427154 chr5:103427133-103427144 chr5:103427134-103427143 chr5:103427132-103427143 chr5:103427134-103427143
20	CEBPB	chr5:103425190-103425358	K562	blood:	n/a	chr5:103425288-103425299
21	CEBPB	chr5:103427128-103427147	H1-hESC	embryonic stem cell:	n/a	chr5:103427132-103427145 chr5:103427134-103427143 chr5:103427134-103427143 chr5:103427132-103427145 chr5:103427132-103427145 chr5:103427132-103427143 chr5:103427133-103427144 chr5:103427134-103427143 chr5:103427132-103427143 chr5:103427134-103427143
22	CEBPB	chr5:103447273-103447500	A549	lung:	n/a	chr5:103447373-103447386
23	CEBPB	chr5:103464057-103464423	A549	lung:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
24	CEBPB	chr5:103447231-103447571	K562	blood:	n/a	chr5:103447512-103447523 chr5:103447373-103447386
25	CEBPB	chr5:103427036-103427225	A549	lung:	n/a	chr5:103427132-103427145 chr5:103427134-103427143 chr5:103427134-103427143 chr5:103427132-103427145 chr5:103427132-103427145 chr5:103427132-103427143 chr5:103427142-103427154 chr5:103427133-103427144 chr5:103427134-103427143 chr5:103427132-103427143 chr5:103427134-103427143
26	CEBPB	chr5:103464067-103464438	MCF-7	breast:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
27	CEBPB	chr5:103424886-103425630	HCT-116	colon:	n/a	chr5:103425288-103425299
28	CEBPB	chr5:103464041-103464452	ECC-1	luminal epithelium:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
29	CEBPB	chr5:103464063-103464386	K562	blood:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
30	CEBPB	chr5:103464069-103464420	Hela-S3	cervix:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
31	CEBPB	chr5:103464137-103464459	A549	lung:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
32	CEBPB	chr5:103467735-103467899	K562	blood:	n/a	n/a
33	CEBPB	chr5:103424899-103425699	HCT-116	colon:	n/a	chr5:103425288-103425299
34	CEBPB	chr5:103464140-103464331	K562	blood:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
35	CEBPB	chr5:103424808-103425495	K562	blood:	n/a	chr5:103425288-103425299
36	CEBPB	chr5:103447171-103447695	HepG2	liver:	n/a	chr5:103447512-103447523 chr5:103447373-103447386
37	CEBPB	chr5:103464056-103464445	K562	blood:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
38	CEBPB	chr5:103426963-103427303	IMR90	lung:	n/a	chr5:103427132-103427145 chr5:103427134-103427143 chr5:103427134-103427143 chr5:103427132-103427145 chr5:103427132-103427145 chr5:103427132-103427143 chr5:103427142-103427154 chr5:103427133-103427144 chr5:103427134-103427143 chr5:103427132-103427143 chr5:103427134-103427143
39	CEBPB	chr5:103464090-103464423	H1-hESC	embryonic stem cell:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
40	CEBPB	chr5:103464068-103464443	IMR90	lung:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
41	CEBPB	chr5:103447457-103447631	HepG2	liver:	n/a	chr5:103447512-103447523
42	CEBPB	chr5:103447219-103447653	Hela-S3	cervix:	n/a	chr5:103447512-103447523 chr5:103447373-103447386
43	CEBPB	chr5:103425252-103425357	HepG2	liver:	n/a	chr5:103425288-103425299
44	CEBPB	chr5:103464067-103464427	A549	lung:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
45	CEBPB	chr5:103416135-103416351	K562	blood:	n/a	n/a
46	CEBPB	chr5:103426962-103427302	K562	blood:	n/a	chr5:103427132-103427145 chr5:103427134-103427143 chr5:103427134-103427143 chr5:103427132-103427145 chr5:103427132-103427145 chr5:103427132-103427143 chr5:103427142-103427154 chr5:103427133-103427144 chr5:103427134-103427143 chr5:103427132-103427143 chr5:103427134-103427143
47	CEBPB	chr5:103424874-103425482	K562	blood:	n/a	chr5:103425288-103425299
48	CEBPB	chr5:103464020-103464552	MCF-7	breast:	n/a	chr5:103464254-103464263 chr5:103464252-103464265 chr5:103464254-103464263 chr5:103464254-103464263
49	CEBPD	chr5:103424768-103425471	K562	blood:	n/a	n/a
50	CEBPD	chr5:103424716-103425279	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:103467212..103468815-chr5:103480734..103482743,2	K562	blood:
2	chr5:103419555..103422324-chr5:103423618..103426898,4	K562	blood:
3	chr5:103457491..103460470-chr5:103461243..103465378,4	K562	blood:
4	chr5:103249220..103251663-chr5:103417841..103420142,2	K562	blood:
5	chr5:103427770..103429780-chr5:103432412..103434956,2	K562	blood:
6	chr12:112035976..112038316-chr5:103433179..103435078,2	MCF-7	breast:
7	chr5:44578647..44579149-chr5:103415633..103416333,2	Hela-S3	cervix:
8	chr5:103472133..103474624-chr5:103476667..103479218,2	K562	blood:
9	chr5:103416241..103417960-chr5:103419579..103421622,2	MCF-7	breast:
10	chr5:102593172..102596932-chr5:103420035..103422975,3	K562	blood:
11	chr5:103432374..103435053-chr5:103436419..103438700,3	MCF-7	breast:
12	chr5:103424892..103429270-chr5:103431386..103433912,4	K562	blood:
13	chr5:103445190..103447987-chr5:103454013..103455945,2	K562	blood:
14	chr5:103424304..103427061-chr5:103434256..103435929,2	K562	blood:
15	chr5:103438292..103439842-chr5:103445545..103447443,2	MCF-7	breast:
16	chr5:103416241..103417960-chr5:103419579..103421622,2	MCF-7	breast:
17	chr5:103471677..103474624-chr5:103476498..103479218,3	K562	blood:
18	chr5:103424892..103427295-chr5:103431386..103434334,3	K562	blood:
19	chr5:103431462..103433805-chr5:103436805..103438651,2	K562	blood:
20	chr5:103424379..103427080-chr5:103428532..103430854,2	K562	blood:
21	chr5:103440945..103442591-chr5:103463038..103465422,2	K562	blood:
22	chr5:103431462..103433805-chr5:103436805..103438651,2	K562	blood:
23	chr5:103457491..103460470-chr5:103461243..103465378,4	K562	blood:
24	chr5:103406028..103408953-chr5:103419618..103421464,2	K562	blood:
25	chr5:103438292..103439842-chr5:103445545..103447443,2	MCF-7	breast:
26	chr5:103419555..103422324-chr5:103423618..103426898,4	K562	blood:
27	chr5:103406028..103408953-chr5:103419618..103421464,2	K562	blood:
28	chr5:103414629..103417722-chr5:103419240..103423591,5	K562	blood:
29	chr5:103424892..103427295-chr5:103431386..103434334,3	K562	blood:
30	chr5:102976878..102978536-chr5:103450055..103452229,2	K562	blood:
31	chr5:103424379..103427080-chr5:103428532..103430854,2	K562	blood:
32	chr5:103440945..103442591-chr5:103463038..103465422,2	K562	blood:
33	chr5:103445190..103447987-chr5:103454013..103455945,2	K562	blood:
34	chr5:103424892..103429270-chr5:103431386..103433912,4	K562	blood:
35	chr5:103469361..103471032-chr5:103473793..103476182,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf30-1	chr5:103441061-103443042	NONHSAT147352
2	lnc-C5orf30-1	chr5:103415612-103415825	ENSG00000251026
3	lnc-C5orf30-1	chr5:103417581-103417648	ENSG00000251026
4	lnc-C5orf30-1	chr5:103439875-103439988	ENSG00000251026
5	lnc-C5orf30-1	chr5:103416609-103416742	ENSG00000251026
6	lnc-C5orf30-1	chr5:103439963-103439988	NONHSAT147352
7	lnc-C5orf30-1	chr5:103441061-103441104	ENSG00000251026

Variant related genes	Relation type
ENSG00000251026	TF binding region
RNU1-140P	TF binding region
ENSG00000204842	chromatin interactions
ENSG00000258099	chromatin interactions
ENSG00000201910	chromatin interactions
ENSG00000251026	chromatin interactions
ENSG00000181751	chromatin interactions

Extended variants
information (count: 1747 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1290515	chr5:103411734-103411735	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs573661710	chr5:103411775-103411776	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542394923	chr5:103411801-103411802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563353840	chr5:103411833-103411834	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs189234255	chr5:103411834-103411835	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs180730850	chr5:103411839-103411840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs544608528	chr5:103411840-103411841	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564798542	chr5:103411842-103411843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs530727837	chr5:103411843-103411844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550331780	chr5:103411844-103411845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs560952476	chr5:103411851-103411852	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs530194119	chr5:103411852-103411853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs201379311	chr5:103411858-103411859	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs138502099	chr5:103411865-103411866	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs111715375	chr5:103411872-103411873	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538607209	chr5:103411907-103411908	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552611855	chr5:103411937-103411938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs569544876	chr5:103411938-103411939	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs538569339	chr5:103411946-103411947	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs1289197	chr5:103411976-103411977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs574976352	chr5:103412006-103412007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536343521	chr5:103412018-103412019	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552747526	chr5:103412135-103412136	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs1289198	chr5:103412160-103412161	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs78342822	chr5:103412163-103412164	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564559519	chr5:103412186-103412187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs531299190	chr5:103415323-103415324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201592667	chr5:103415332-103415333	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs568066714	chr5:103415339-103415340	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs533744112	chr5:103415344-103415345	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs547435024	chr5:103415365-103415366	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs570732980	chr5:103415373-103415374	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551676216	chr5:103415378-103415379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs376595949	chr5:103415379-103415380	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs539774259	chr5:103415382-103415383	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs76088368	chr5:103415387-103415388	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs202069783	chr5:103415388-103415389	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs376479388	chr5:103415412-103415413	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs369986508	chr5:103415414-103415415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs576224152	chr5:103415422-103415423	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs373875115	chr5:103415433-103415434	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs535572757	chr5:103415446-103415447	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs368800439	chr5:103415454-103415455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs555781882	chr5:103415468-103415469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs572457015	chr5:103415471-103415472	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs377337014	chr5:103415594-103415595	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184852795	chr5:103415605-103415606	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs577893858	chr5:103415607-103415608	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs543747597	chr5:103415618-103415619	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs377598415	chr5:103415621-103415622	Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103415600-103416800	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr5:103416000-103417600	Active TSS	K562	blood
3	chr5:103416200-103416800	Active TSS	A549	lung
4	chr5:103416200-103417000	Active TSS	HepG2	liver
5	chr5:103416400-103416800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:103416800-103419200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:103417600-103417800	Transcr. at gene 5' and 3'	K562	blood
8	chr5:103417800-103418000	Active TSS	K562	blood
9	chr5:103418000-103423400	Weak transcription	K562	blood
10	chr5:103418800-103419000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:103419200-103419600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:103419200-103420800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr5:103419600-103425000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr5:103420200-103422800	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr5:103422800-103424800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr5:103423400-103424800	Enhancers	K562	blood
17	chr5:103424800-103425200	Flanking Active TSS	K562	blood
18	chr5:103425000-103425200	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr5:103425000-103425200	Enhancers	NH-A	brain
20	chr5:103425000-103425400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr5:103425000-103425800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr5:103425200-103425400	Active TSS	K562	blood
23	chr5:103425200-103425600	Enhancers	H9 Cell Line	embryonic stem cell
24	chr5:103425400-103425800	Flanking Active TSS	K562	blood
25	chr5:103425800-103440800	Weak transcription	K562	blood
26	chr5:103438600-103442800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr5:103446600-103447200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:103447000-103447600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:103447000-103447800	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr5:103450400-103457600	Weak transcription	K562	blood
31	chr5:103452000-103452600	Enhancers	HUVEC	blood vessel
32	chr5:103462000-103463000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:103472200-103474400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr5:103472400-103473600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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