Variant report

Variant	esv1825644
Chromosome Location	chr5:127427533-127450581
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	BATF	chr5:127447799-127448079	GM12878	blood:	n/a	chr5:127447970-127447980 chr5:127447969-127447980
2	CBX3	chr5:127433433-127433849	K562	blood:	n/a	n/a
3	CBX3	chr5:127432966-127433321	K562	blood:	n/a	n/a
4	CEBPB	chr5:127437359-127437630	K562	blood:	n/a	n/a
5	CEBPB	chr5:127449336-127449585	HepG2	liver:	n/a	chr5:127449479-127449490
6	CEBPB	chr5:127429551-127429653	A549	lung:	n/a	n/a
7	CEBPB	chr5:127437319-127437646	K562	blood:	n/a	n/a
8	CTCF	chr5:127445011-127445066	MCF-7	breast:	n/a	n/a
9	CTCF	chr5:127427920-127428070	GM12873	blood:	n/a	n/a
10	CTCF	chr5:127428000-127428150	MCF-7	breast:	n/a	n/a
11	CTCF	chr5:127437549-127437648	Medullo	brain:	n/a	n/a
12	CTCF	chr5:127427980-127428130	BE2_C	brain:	n/a	n/a
13	CTCF	chr5:127427980-127428130	HEK293	kidney:	n/a	n/a
14	CTCF	chr5:127428080-127428230	A549	lung:	n/a	n/a
15	CTCF	chr5:127437560-127437710	HMEC	breast:	n/a	n/a
16	CTCF	chr5:127428000-127428150	HRE	kidney:	n/a	n/a
17	CTCF	chr5:127427980-127428130	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr5:127437457-127437673	GM12878	blood:	n/a	n/a
19	CTCF	chr5:127445551-127445628	GM13976	blood:	n/a	n/a
20	CTCF	chr5:127428120-127428270	BE2_C	brain:	n/a	n/a
21	E2F4	chr5:127429854-127430054	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr5:127441895-127442095	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr5:127447965-127448165	MCF10A-Er-Src	breast:	n/a	n/a
24	EBF1	chr5:127434389-127434549	GM12878	blood:	n/a	chr5:127434470-127434483
25	EP300	chr5:127437453-127437735	K562	blood:	n/a	n/a
26	FOS	chr5:127447840-127448171	HUVEC	blood vessel:	n/a	chr5:127447971-127447982 chr5:127447973-127447981 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982
27	FOS	chr5:127447876-127448057	MCF10A-Er-Src	breast:	n/a	chr5:127447971-127447982 chr5:127447973-127447981 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982
28	FOS	chr5:127429129-127429469	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:127447892-127448092	MCF10A-Er-Src	breast:	n/a	chr5:127447971-127447982 chr5:127447973-127447981 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982
30	FOS	chr5:127429109-127429454	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr5:127437000-127437163	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr5:127429129-127429458	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:127436996-127437166	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr5:127429129-127429471	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:127447820-127448069	MCF10A-Er-Src	breast:	n/a	chr5:127447971-127447982 chr5:127447973-127447981 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982 chr5:127447972-127447982
36	FOS	chr5:127437041-127437060	MCF10A-Er-Src	breast:	n/a	n/a
37	FOSL2	chr5:127438147-127438361	HepG2	liver:	n/a	n/a
38	FOXM1	chr5:127447711-127448083	GM12878	blood:	n/a	n/a
39	IRF1	chr5:127432662-127432674	K562	blood:	n/a	n/a
40	JUN	chr5:127429225-127429428	HepG2	liver:	n/a	n/a
41	JUN	chr5:127429124-127429452	HUVEC	blood vessel:	n/a	n/a
42	JUN	chr5:127429214-127429464	K562	blood:	n/a	n/a
43	JUND	chr5:127429120-127429492	HepG2	liver:	n/a	chr5:127429288-127429299
44	JUND	chr5:127428887-127429618	SK-N-SH	brain:	n/a	chr5:127429288-127429299
45	KAP1	chr5:127432860-127433996	K562	blood:	n/a	n/a
46	MAFF	chr5:127436891-127437095	K562	blood:	n/a	n/a
47	MAFK	chr5:127436863-127437148	IMR90	lung:	n/a	chr5:127436989-127437006
48	MAFK	chr5:127447880-127448103	IMR90	lung:	n/a	n/a
49	MAFK	chr5:127436929-127437049	HepG2	liver:	n/a	chr5:127436989-127437006
50	MAFK	chr5:127436841-127437152	HepG2	liver:	n/a	chr5:127436989-127437006

No.	Distal block	Cell Line	Cell type
1	chr5:127372368..127374047-chr5:127433915..127436098,2	K562	blood:
2	chr5:127434040..127436048-chr5:127444617..127446605,2	K562	blood:
3	chr5:127427255..127429514-chr5:127437565..127440118,2	MCF-7	breast:
4	chr5:127419054..127420642-chr5:127435156..127436795,2	MCF-7	breast:
5	chr5:127428726..127433227-chr5:127434885..127438247,5	K562	blood:
6	chr5:127428694..127433227-chr5:127434862..127437524,4	K562	blood:
7	chr5:127425561..127430012-chr5:127430548..127434724,5	K562	blood:
8	chr5:127418504..127420924-chr5:127441189..127443257,2	MCF-7	breast:
9	chr5:127417604..127421572-chr5:127435124..127437256,5	K562	blood:
10	chr5:127416711..127418835-chr5:127436725..127439641,2	MCF-7	breast:
11	chr5:127417788..127421083-chr5:127443681..127446699,3	K562	blood:
12	chr5:127432801..127435148-chr5:127441508..127443788,3	K562	blood:
13	chr5:127428694..127433227-chr5:127434862..127437524,4	K562	blood:
14	chr5:127428726..127433227-chr5:127434885..127438247,5	K562	blood:
15	chr5:127425199..127427763-chr5:127441097..127443720,2	MCF-7	breast:
16	chr5:127447046..127449842-chr5:127451576..127454099,2	K562	blood:
17	chr5:127416395..127419200-chr5:127437318..127440237,2	K562	blood:
18	chr5:127435818..127437710-chr5:127440981..127443609,2	K562	blood:
19	chr5:127435818..127437710-chr5:127440981..127443609,2	K562	blood:
20	chr5:127432707..127435327-chr5:127438169..127440618,3	K562	blood:
21	chr5:127425561..127430012-chr5:127430548..127434724,5	K562	blood:
22	chr5:127429085..127432949-chr5:127432984..127436984,4	MCF-7	breast:
23	chr5:127419046..127421214-chr5:127431481..127433542,2	K562	blood:
24	chr5:127425199..127427763-chr5:127441097..127443720,2	MCF-7	breast:
25	chr5:127418832..127420941-chr5:127446155..127448074,2	MCF-7	breast:
26	chr5:127427255..127429514-chr5:127437565..127440118,2	MCF-7	breast:
27	chr5:127418269..127421546-chr5:127449904..127452923,3	MCF-7	breast:
28	chr5:127432801..127435148-chr5:127441508..127443788,3	K562	blood:
29	chr5:127429085..127432949-chr5:127432984..127436984,4	MCF-7	breast:
30	chr5:127432707..127435327-chr5:127438169..127440618,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC27A6-2	chr5:127445178-127446686	NONHSAT103657
2	lnc-FBN2-7	chr5:127446561-127446665	ucscGeneNc_uc003kun_2

Variant related genes	Relation type
KDELC1P1	TF binding region
ENSG00000245937	chromatin interactions
ENSG00000250329	chromatin interactions
ENSG00000064651	chromatin interactions

Extended variants
information (count: 829 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10067555	chr5:127427533-127427534	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79262065	chr5:127427540-127427541	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs138309024	chr5:127427551-127427552	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs373293654	chr5:127427566-127427567	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs377463787	chr5:127427587-127427588	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs573602939	chr5:127427599-127427600	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs376298116	chr5:127427636-127427637	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs559202826	chr5:127427692-127427693	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs575860832	chr5:127427727-127427728	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs369289224	chr5:127427758-127427759	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs368340377	chr5:127427774-127427775	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs184861979	chr5:127427809-127427810	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs141823822	chr5:127427822-127427823	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs542633999	chr5:127427835-127427836	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs189586871	chr5:127427841-127427842	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs559213155	chr5:127427875-127427876	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs528381664	chr5:127427879-127427880	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs112389004	chr5:127427914-127427915	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs571208474	chr5:127427917-127427918	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs530658688	chr5:127427978-127427979	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs550487781	chr5:127428026-127428027	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs150173744	chr5:127428063-127428064	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs536322875	chr5:127428072-127428073	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs17675580	chr5:127428080-127428081	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs111454575	chr5:127428111-127428112	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs181597534	chr5:127428121-127428122	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs559339072	chr5:127428125-127428126	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs149310769	chr5:127428176-127428177	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs544821686	chr5:127428226-127428227	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs544561460	chr5:127428263-127428264	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs554841121	chr5:127428264-127428265	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs146244744	chr5:127428282-127428283	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542319171	chr5:127428326-127428327	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs139264950	chr5:127428416-127428417	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534910011	chr5:127428421-127428422	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs554768774	chr5:127428425-127428426	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574674897	chr5:127428593-127428594	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs74555060	chr5:127428634-127428635	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs576680783	chr5:127428640-127428641	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs370725601	chr5:127428661-127428662	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544598139	chr5:127428731-127428732	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs564870119	chr5:127428741-127428742	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs563624972	chr5:127428760-127428761	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs186255851	chr5:127428771-127428772	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs7713860	chr5:127428789-127428790	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs190276711	chr5:127428790-127428791	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs142473699	chr5:127428803-127428804	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs530220149	chr5:127428818-127428819	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs375041740	chr5:127428825-127428826	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs566966892	chr5:127428833-127428834	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127420800-127429600	Weak transcription	Aorta	Aorta
2	chr5:127421000-127428200	Weak transcription	HSMM	muscle
3	chr5:127421000-127429600	Weak transcription	Gastric	stomach
4	chr5:127421000-127431600	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr5:127421200-127431400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr5:127421400-127429400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr5:127421400-127436400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:127421400-127450200	Weak transcription	Fetal Thymus	thymus
9	chr5:127421600-127429000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr5:127421600-127429800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr5:127421600-127432400	Weak transcription	Colon Smooth Muscle	Colon
12	chr5:127421600-127432400	Weak transcription	NHDF-Ad	bronchial
13	chr5:127421600-127432600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr5:127421600-127466800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:127422000-127433200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:127422000-127434200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:127422200-127428800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr5:127422400-127431400	Weak transcription	HMEC	breast
19	chr5:127422800-127428800	Weak transcription	Primary T cells from cord blood	blood
20	chr5:127422800-127431400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:127423000-127428000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr5:127423000-127428800	Weak transcription	Stomach Mucosa	stomach
23	chr5:127423000-127436600	Weak transcription	HSMMtube	muscle
24	chr5:127423400-127427600	Weak transcription	HUVEC	blood vessel
25	chr5:127423400-127429400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr5:127423600-127428800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr5:127423600-127431200	Weak transcription	A549	lung
28	chr5:127423600-127432200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr5:127423600-127436400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr5:127423600-127444800	Weak transcription	Fetal Stomach	stomach
31	chr5:127423600-127494000	Weak transcription	K562	blood
32	chr5:127423800-127428000	Weak transcription	Ovary	ovary
33	chr5:127423800-127429200	Weak transcription	Dnd41	blood
34	chr5:127425200-127428800	Weak transcription	Fetal Intestine Small	intestine
35	chr5:127425800-127428800	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr5:127425800-127445000	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr5:127426400-127427600	Weak transcription	Brain Angular Gyrus	brain
38	chr5:127426400-127428200	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr5:127426400-127430600	Strong transcription	Primary B cells from cord blood	blood
40	chr5:127426400-127431600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr5:127426600-127427800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr5:127426600-127427800	Weak transcription	Left Ventricle	heart
43	chr5:127426800-127427800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr5:127426800-127428000	Weak transcription	Brain Hippocampus Middle	brain
45	chr5:127426800-127433400	Weak transcription	Small Intestine	intestine
46	chr5:127427000-127428200	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr5:127427000-127428800	Weak transcription	Brain Substantia Nigra	brain
48	chr5:127427000-127429400	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr5:127427000-127429600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr5:127427200-127428600	Active TSS	Duodenum Mucosa	Duodenum

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