Variant report

Variant	esv2755740
Chromosome Location	chr5:115576139-115633474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:115614176-115614178	K562	blood:	n/a	n/a
2	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
3	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
4	CBX3	chr5:115612735-115612979	K562	blood:	n/a	n/a
5	CBX3	chr5:115612612-115613059	HCT-116	colon:	n/a	n/a
6	CBX3	chr5:115612653-115612965	K562	blood:	n/a	n/a
7	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
8	CEBPB	chr5:115584226-115584373	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
9	CEBPB	chr5:115632480-115632726	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
11	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
12	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
14	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
15	CEBPB	chr5:115615956-115616164	HepG2	liver:	n/a	n/a
16	CEBPB	chr5:115584135-115584482	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
17	CEBPB	chr5:115584254-115584389	K562	blood:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
18	CEBPB	chr5:115584119-115584488	MCF-7	breast:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
19	CEBPB	chr5:115612611-115612811	A549	lung:	n/a	n/a
20	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
21	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
22	CTCF	chr5:115608340-115608490	HCT-116	colon:	n/a	n/a
23	CTCF	chr5:115608440-115608590	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr5:115608380-115608530	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr5:115608320-115608470	GM12872	blood:	n/a	n/a
26	CTCF	chr5:115608440-115608590	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr5:115625120-115625270	SAEC	small airway:	n/a	chr5:115625169-115625182
28	CTCF	chr5:115608360-115608510	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr5:115625160-115625310	HEK293	kidney:	n/a	chr5:115625169-115625182
30	CTCF	chr5:115625106-115625257	MCF-7	breast:	n/a	chr5:115625169-115625182
31	CTCF	chr5:115608320-115608470	RPTEC	kidney:	n/a	n/a
32	CTCF	chr5:115625120-115625270	AG04450	lung:	n/a	chr5:115625169-115625182
33	CTCF	chr5:115625100-115625250	A549	lung:	n/a	chr5:115625169-115625182
34	CTCF	chr5:115625220-115625370	GM12878	blood:	n/a	n/a
35	CTCF	chr5:115633172-115633465	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr5:115625040-115625190	AG09319	gingival:	n/a	chr5:115625169-115625182
37	CTCF	chr5:115614780-115614930	BJ	skin:	n/a	n/a
38	CTCF	chr5:115625088-115625282	H1-hESC	embryonic stem cell:	n/a	chr5:115625169-115625182
39	CTCF	chr5:115625080-115625230	Hela-S3	cervix:	n/a	chr5:115625169-115625182
40	CTCF	chr5:115633274-115633363	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:115625080-115625230	HPAF	blood vessel:	n/a	chr5:115625169-115625182
42	CTCF	chr5:115625100-115625250	GM12868	blood:	n/a	chr5:115625169-115625182
43	CTCF	chr5:115608420-115608570	GM12872	blood:	n/a	n/a
44	CTCF	chr5:115625060-115625210	HBMEC	blood vessel:	n/a	chr5:115625169-115625182
45	CTCF	chr5:115608355-115608631	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:115624940-115625090	GM12866	blood:	n/a	n/a
47	CTCF	chr5:115625000-115625150	GM12872	blood:	n/a	n/a
48	CTCF	chr5:115625160-115625310	GM06990	blood:	n/a	chr5:115625169-115625182
49	CTCF	chr5:115608140-115608290	AG09309	skin:	n/a	n/a
50	CTCF	chr5:115608420-115608570	GM12873	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115599680-115599730	Hepatocyte	liver:	n/a
2	chr5:115599680-115599730	NH-A	brain:	n/a
3	chr5:115599680-115599730	ProgFib	skin:	n/a
4	chr5:115599680-115599730	HUVEC	blood vessel:	n/a
5	chr5:115599680-115599730	MCF10A-Er-Src	breast:	n/a
6	chr5:115599680-115599730	PrEC	prostate:	n/a
7	chr5:115599680-115599730	CMK	blood:	n/a
8	chr5:115599680-115599730	ovcar-3	ovarian:	n/a
9	chr5:115599680-115599730	PANC-1	pancreas:	n/a
10	chr5:115599680-115599730	GM12891	blood:	n/a
11	chr5:115599680-115599730	AG04450	lung:	fetal
12	chr5:115599680-115599730	GM06990	blood:	n/a
13	chr5:115599680-115599730	HIPEpiC	eye:	n/a
14	chr5:115599680-115599730	MCF-7	breast:	n/a
15	chr5:115599680-115599730	AG09319	gingival:	n/a
16	chr5:115599680-115599730	BJ	skin:	n/a
17	chr5:115599680-115599730	HRE	kidney:	n/a
18	chr5:115599680-115599730	BE2_C	brain:	n/a
19	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:115599680-115599730	SAEC	small airway:	n/a
21	chr5:115599680-115599730	HRPEpiC	eye:	n/a
22	chr5:115599680-115599730	HRCEpiC	kidney:	n/a
23	chr5:115599680-115599730	HEK293	kidney:	embryo
24	chr5:115599680-115599730	PFSK-1	brain:	n/a
25	chr5:115599680-115599730	HAEpiC	amniotic membrane:	n/a
26	chr5:115599680-115599730	U87	brain:	n/a
27	chr5:115599680-115599730	HCPEpiC	choroid plexus:	n/a
28	chr5:115599680-115599730	GM12878	blood:	n/a
29	chr5:115599680-115599730	HCT-116	colon:	n/a
30	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
31	chr5:115599680-115599730	AG04449	skin:	fetal
32	chr5:115599680-115599730	SK-N-SH	brain:	n/a
33	chr5:115599680-115599730	NB4	blood:	n/a
34	chr5:115599680-115599730	H1-hESC	embryonic stem cell:	embryo
35	chr5:115599680-115599730	Jurkat	blood:	n/a
36	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
37	chr5:115599680-115599730	NHBE	bronchial:	n/a
38	chr5:115599680-115599730	HMEC	breast:	n/a
39	chr5:115599680-115599730	GM12892	blood:	n/a
40	chr5:115599680-115599730	HepG2	liver:	n/a
41	chr5:115599680-115599730	RPTEC	kidney:	n/a
42	chr5:115599680-115599730	AG10803	skin:	n/a
43	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
44	chr5:115599680-115599730	T-47D	breast:	n/a
45	chr5:115599680-115599730	HCM	heart:	n/a
46	chr5:115599680-115599730	A549	lung:	n/a
47	chr5:115599680-115599730	AG09309	skin:	n/a
48	chr5:115599680-115599730	NHDF-neo	bronchial:	n/a
49	chr5:115599680-115599730	Caco-2	colon:	n/a
50	chr5:115599680-115599730	SKMC	muscle:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
2	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
3	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
4	chr5:115473058..115473763-chr5:115624723..115625238,2	MCF-7	breast:
5	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
6	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
7	chr20:47537809..47538621-chr5:115628215..115629028,2	MCF-7	breast:
8	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
9	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
10	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LVRN.1-4	chr5:115632111-115632653	NONHSAT103359
2	lnc-LVRN.1-4	chr5:115628154-115628257	NONHSAT103358

No data

Variant related genes	Relation type
COMMD10	TF binding region
COMMD10	CpG island
ENSG00000124198	chromatin interactions

Extended variants
information (count: 2988 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2988 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17139253	chr5:115576139-115576140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564926093	chr5:115576197-115576198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34656944	chr5:115576227-115576228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17139256	chr5:115576232-115576233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs376888154	chr5:115576287-115576288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541686180	chr5:115576300-115576301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528009655	chr5:115576315-115576316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562492403	chr5:115576342-115576343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530334324	chr5:115576345-115576346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117470479	chr5:115576350-115576351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187965388	chr5:115576412-115576413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572478027	chr5:115576423-115576424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549684823	chr5:115576506-115576507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192445505	chr5:115576516-115576517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182731783	chr5:115576519-115576520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571207503	chr5:115576531-115576532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533871410	chr5:115576553-115576554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547684340	chr5:115576563-115576564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567407315	chr5:115576567-115576568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536040333	chr5:115576584-115576585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188154299	chr5:115576617-115576618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538434682	chr5:115576630-115576631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529112838	chr5:115576635-115576636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571326589	chr5:115576659-115576660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191741085	chr5:115576714-115576715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569853002	chr5:115576731-115576732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376225337	chr5:115576773-115576774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12659076	chr5:115576799-115576800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184552934	chr5:115576821-115576822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72806914	chr5:115576830-115576831	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs541198095	chr5:115576866-115576867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555254760	chr5:115576876-115576877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368978854	chr5:115576908-115576909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138272424	chr5:115576909-115576910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544077158	chr5:115576939-115576940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563864108	chr5:115576995-115576996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114990314	chr5:115577059-115577060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545104006	chr5:115577073-115577074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4921084	chr5:115577074-115577075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs188915693	chr5:115577110-115577111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192569061	chr5:115577191-115577192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567597183	chr5:115577227-115577228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184796478	chr5:115577236-115577237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549597798	chr5:115577242-115577243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569489039	chr5:115577265-115577266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150574868	chr5:115577280-115577281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538416483	chr5:115577284-115577285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144952029	chr5:115577285-115577286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71734162	chr5:115577316-115577317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs61328599	chr5:115577326-115577327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115551800-115576400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr5:115557400-115580800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr5:115557400-115583200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr5:115559200-115578400	Weak transcription	Fetal Lung	lung
5	chr5:115560400-115581000	Weak transcription	Primary T cells from cord blood	blood
6	chr5:115560400-115610600	Weak transcription	Left Ventricle	heart
7	chr5:115561400-115580000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr5:115561800-115586400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr5:115562400-115589000	Weak transcription	Ovary	ovary
10	chr5:115568400-115578800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr5:115569600-115577600	Weak transcription	Fetal Kidney	kidney
12	chr5:115569800-115582200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:115572000-115580400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:115573000-115578800	Weak transcription	Primary B cells from cord blood	blood
15	chr5:115574000-115580000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr5:115575000-115578200	Weak transcription	Colon Smooth Muscle	Colon
17	chr5:115576200-115576400	Enhancers	Adipose Nuclei	Adipose
18	chr5:115576200-115576600	Enhancers	HUVEC	blood vessel
19	chr5:115577600-115579600	Enhancers	Fetal Kidney	kidney
20	chr5:115577800-115578800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr5:115578000-115578800	Enhancers	Adipose Nuclei	Adipose
22	chr5:115578200-115578600	Enhancers	Liver	Liver
23	chr5:115578200-115578800	Enhancers	Colon Smooth Muscle	Colon
24	chr5:115578200-115579000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr5:115578400-115578600	Enhancers	Fetal Lung	lung
26	chr5:115578800-115579000	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr5:115578800-115579600	Strong transcription	Primary B cells from cord blood	blood
28	chr5:115578800-115586000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:115579600-115581800	Weak transcription	Fetal Intestine Large	intestine
30	chr5:115579600-115610600	Weak transcription	Primary B cells from cord blood	blood
31	chr5:115580400-115580800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:115581000-115581200	Strong transcription	Primary T cells from cord blood	blood
33	chr5:115581200-115581400	ZNF genes & repeats	Primary T cells from cord blood	blood
34	chr5:115581400-115591600	Weak transcription	Primary T cells from cord blood	blood
35	chr5:115581800-115582600	ZNF genes & repeats	Fetal Intestine Large	intestine
36	chr5:115582600-115594600	Weak transcription	Fetal Intestine Large	intestine
37	chr5:115583000-115583200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:115583600-115589000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:115583800-115586200	Weak transcription	Brain Hippocampus Middle	brain
40	chr5:115584200-115586200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr5:115584800-115603600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:115585200-115587800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:115585600-115586400	Weak transcription	Dnd41	blood
44	chr5:115585800-115586000	Weak transcription	Primary hematopoietic stem cells	blood
45	chr5:115585800-115601200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr5:115586000-115587000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:115586200-115586600	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr5:115586200-115586800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
49	chr5:115586200-115586800	Strong transcription	Brain Hippocampus Middle	brain
50	chr5:115586400-115586600	Enhancers	Aorta	Aorta

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