Variant report

Variant	nsv829768
Chromosome Location	chr3:157832878-158012070
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:833)
CpG islands
(count:0)
Chromatin interactive
region (count:83)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:157842545-157842553	K562	blood:	n/a	n/a
2	ARID3A	chr3:157885650-157886349	K562	blood:	n/a	n/a
3	ARID3A	chr3:157897158-157897252	K562	blood:	n/a	n/a
4	ARID3A	chr3:157836066-157836216	K562	blood:	n/a	n/a
5	ARID3A	chr3:157877545-157877863	K562	blood:	n/a	n/a
6	ARID3A	chr3:157885995-157886199	HepG2	liver:	n/a	n/a
7	ATF1	chr3:157836048-157836255	K562	blood:	n/a	n/a
8	ATF1	chr3:157885659-157886228	K562	blood:	n/a	n/a
9	ATF2	chr3:157839088-157839404	GM12878	blood:	n/a	n/a
10	ATF3	chr3:157835669-157836132	K562	blood:	n/a	n/a
11	ATF3	chr3:157885843-157886303	K562	blood:	n/a	n/a
12	BACH1	chr3:157885891-157886392	K562	blood:	n/a	n/a
13	BACH1	chr3:157845645-157845975	H1-hESC	embryonic stem cell:	n/a	chr3:157845816-157845830
14	BACH1	chr3:157890633-157890678	K562	blood:	n/a	n/a
15	BATF	chr3:157839154-157839350	GM12878	blood:	n/a	n/a
16	BATF	chr3:157923752-157924020	GM12878	blood:	n/a	n/a
17	BATF	chr3:157870032-157870280	GM12878	blood:	n/a	chr3:157870170-157870181
18	BCL3	chr3:157877506-157877822	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:157885654-157886212	K562	blood:	n/a	n/a
20	BHLHE40	chr3:157835999-157836462	K562	blood:	n/a	n/a
21	BRCA1	chr3:157885810-157886403	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr3:157977466-157977505	GM12878	blood:	n/a	n/a
23	CBX3	chr3:157918693-157919218	K562	blood:	n/a	n/a
24	CBX3	chr3:157885462-157886336	HCT-116	colon:	n/a	n/a
25	CBX3	chr3:157916775-157917147	K562	blood:	n/a	n/a
26	CBX3	chr3:157845566-157846106	HCT-116	colon:	n/a	n/a
27	CBX3	chr3:157878602-157879309	HCT-116	colon:	n/a	n/a
28	CBX3	chr3:157984712-157985175	HCT-116	colon:	n/a	n/a
29	CBX3	chr3:157840940-157841380	K562	blood:	n/a	n/a
30	CBX3	chr3:157835736-157836445	K562	blood:	n/a	n/a
31	CBX3	chr3:157845064-157845444	K562	blood:	n/a	n/a
32	CBX3	chr3:157918678-157919165	K562	blood:	n/a	n/a
33	CBX3	chr3:157984713-157985314	K562	blood:	n/a	n/a
34	CBX3	chr3:157984774-157985359	K562	blood:	n/a	n/a
35	CBX3	chr3:157878567-157879324	HCT-116	colon:	n/a	n/a
36	CCNT2	chr3:157885632-157886150	K562	blood:	n/a	n/a
37	CEBPB	chr3:157885839-157886399	IMR90	lung:	n/a	chr3:157886197-157886208 chr3:157886358-157886370
38	CEBPB	chr3:157886004-157886371	A549	lung:	n/a	chr3:157886197-157886208 chr3:157886358-157886370
39	CEBPB	chr3:157846579-157847298	HepG2	liver:	n/a	chr3:157846742-157846753
40	CEBPB	chr3:157869453-157869675	IMR90	lung:	n/a	chr3:157869608-157869619
41	CEBPB	chr3:157883014-157883242	K562	blood:	n/a	chr3:157883101-157883114 chr3:157883103-157883114
42	CEBPB	chr3:157857793-157857947	K562	blood:	n/a	n/a
43	CEBPB	chr3:157846560-157847297	K562	blood:	n/a	chr3:157846742-157846753
44	CEBPB	chr3:157838753-157839362	K562	blood:	n/a	chr3:157838870-157838883 chr3:157838872-157838883 chr3:157838870-157838883
45	CEBPB	chr3:157846568-157847152	IMR90	lung:	n/a	chr3:157846742-157846753
46	CEBPB	chr3:157885655-157886555	HCT-116	colon:	n/a	chr3:157886197-157886208 chr3:157886358-157886370
47	CEBPB	chr3:157846652-157846836	H1-hESC	embryonic stem cell:	n/a	chr3:157846742-157846753
48	CEBPB	chr3:157885852-157886403	Hela-S3	cervix:	n/a	chr3:157886197-157886208 chr3:157886358-157886370
49	CEBPB	chr3:157878750-157879075	A549	lung:	n/a	n/a
50	CEBPB	chr3:157885765-157886503	A549	lung:	n/a	chr3:157886197-157886208 chr3:157886358-157886370

No data

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:157838685..157841210-chr3:157855039..157857815,2	K562	blood:
2	chr3:157827031..157829785-chr3:157831722..157834034,6	MCF-7	breast:
3	chr3:157987978..157990899-chr3:157994942..157996783,2	MCF-7	breast:
4	chr3:157849729..157851539-chr3:157855010..157858229,4	K562	blood:
5	chr3:157832385..157834258-chr3:157841919..157844259,2	K562	blood:
6	chr3:157823071..157825253-chr3:157850410..157852335,2	K562	blood:
7	chr3:157889102..157890934-chr3:157896521..157898040,2	MCF-7	breast:
8	chr3:157889156..157891158-chr3:157895026..157897482,2	K562	blood:
9	chr3:157930356..157934544-chr3:157935116..157938081,3	MCF-7	breast:
10	chr3:157833746..157835863-chr3:157852221..157854631,2	MCF-7	breast:
11	chr3:157935014..157937097-chr3:157940736..157943383,2	K562	blood:
12	chr3:157865805..157868312-chr3:157870021..157871959,2	K562	blood:
13	chr3:157832385..157834258-chr3:157841919..157844259,2	K562	blood:
14	chr3:157942867..157945587-chr3:157947255..157949250,2	MCF-7	breast:
15	chr3:157840416..157842184-chr3:157852166..157854407,2	MCF-7	breast:
16	chr3:157840416..157842184-chr3:157852166..157854407,2	MCF-7	breast:
17	chr3:157918972..157921649-chr3:157988884..157990990,2	K562	blood:
18	chr3:157930315..157932972-chr3:157950342..157951863,2	K562	blood:
19	chr3:157825779..157828416-chr3:157891172..157893441,3	K562	blood:
20	chr3:157822052..157824855-chr3:157834788..157837855,4	K562	blood:
21	chr3:157981139..157982745-chr3:157990643..157992701,2	K562	blood:
22	chr3:157921034..157923673-chr3:157931290..157933700,2	K562	blood:
23	chr3:157988669..157990531-chr3:157993629..157996480,3	K562	blood:
24	chr3:157849729..157852576-chr3:157856575..157858121,2	K562	blood:
25	chr3:157839952..157841696-chr3:157860084..157861712,2	K562	blood:
26	chr3:157838373..157839974-chr3:157841476..157843018,2	K562	blood:
27	chr3:157863466..157866461-chr3:157886047..157887794,2	K562	blood:
28	chr3:157882190..157883909-chr3:157890033..157892770,2	K562	blood:
29	chr3:157826605..157829792-chr3:157838040..157843107,6	K562	blood:
30	chr3:157825957..157829751-chr3:157834777..157838011,4	K562	blood:
31	chr3:157835764..157837989-chr3:157840263..157842524,2	K562	blood:
32	chr3:157827136..157830163-chr3:157858698..157861744,3	K562	blood:
33	chr3:157907378..157909218-chr3:157917201..157920072,2	K562	blood:
34	chr3:157836454..157837989-chr3:157840263..157841984,2	K562	blood:
35	chr3:157827329..157829457-chr3:157867998..157870807,2	K562	blood:
36	chr3:157889156..157892699-chr3:157895026..157898968,4	K562	blood:
37	chr3:157880003..157882017-chr3:157883893..157885646,2	K562	blood:
38	chr3:157822716..157824770-chr3:157852147..157853767,2	K562	blood:
39	chr3:157930315..157932972-chr3:157950342..157951863,2	K562	blood:
40	chr3:157989031..157991493-chr3:157993072..157995129,2	K562	blood:
41	chr3:157865805..157868312-chr3:157870021..157871959,2	K562	blood:
42	chr3:157921324..157922851-chr3:157926658..157929146,2	K562	blood:
43	chr3:157849729..157851539-chr3:157855010..157858229,4	K562	blood:
44	chr3:157832507..157834530-chr3:157835792..157838744,2	MCF-7	breast:
45	chr3:157987978..157990899-chr3:157994942..157996783,2	MCF-7	breast:
46	chr3:157825779..157828416-chr3:157891172..157893441,2	K562	blood:
47	chr3:157880003..157882017-chr3:157883893..157885646,2	K562	blood:
48	chr3:157856122..157858271-chr3:157860097..157863022,2	K562	blood:
49	chr3:157907378..157909218-chr3:157917201..157920072,2	K562	blood:
50	chr3:157889742..157892494-chr3:157900682..157903082,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHOX2-3	chr3:157873661-157876196	refGeneNc_1685_NR_027954
2	lnc-SHOX2-8	chr3:157947831-157950897	ucscGeneNc_uc003fax_1
3	lnc-SHOX2-8	chr3:157951578-157951666	ucscGeneNc_uc003fax_1

No data

Variant related genes	Relation type
ENSG00000241723	TF binding region
RSRC1	TF binding region
ENSG00000174891	chromatin interactions
ENSG00000241723	chromatin interactions
ENSG00000168779	chromatin interactions

Extended variants
information (count: 6734 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6734 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182024006	chr3:157832902-157832903	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376668032	chr3:157832903-157832904	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531266812	chr3:157832932-157832933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs562236318	chr3:157832948-157832949	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186158809	chr3:157832966-157832967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544433115	chr3:157832973-157832974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12696067	chr3:157832974-157832975	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs113805268	chr3:157833014-157833015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532828453	chr3:157833084-157833085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551082486	chr3:157833094-157833095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559841576	chr3:157833102-157833103	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527276795	chr3:157833283-157833284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373908475	chr3:157833359-157833360	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190624015	chr3:157833370-157833371	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567443920	chr3:157833380-157833381	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182762777	chr3:157833423-157833424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549667591	chr3:157833431-157833432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147307060	chr3:157833439-157833440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186651309	chr3:157833442-157833443	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190983584	chr3:157833485-157833486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558270592	chr3:157833498-157833499	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573417655	chr3:157833523-157833524	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1608099	chr3:157833589-157833590	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs1608100	chr3:157833633-157833634	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs574211380	chr3:157833634-157833635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544905904	chr3:157833700-157833701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1608101	chr3:157833707-157833708	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs577792689	chr3:157833726-157833727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs74370959	chr3:157833826-157833827	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571377322	chr3:157833870-157833871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs151156188	chr3:157833871-157833872	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs114841073	chr3:157833896-157833897	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140944791	chr3:157833906-157833907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182884459	chr3:157833922-157833923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs560946998	chr3:157833966-157833967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs144687953	chr3:157833990-157833991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550029585	chr3:157834023-157834024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535751527	chr3:157834106-157834107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538707173	chr3:157834145-157834146	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571606008	chr3:157834156-157834157	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538829632	chr3:157834183-157834184	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187746425	chr3:157834291-157834292	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191420307	chr3:157834317-157834318	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538828910	chr3:157834321-157834322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183503882	chr3:157834331-157834332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555441818	chr3:157834408-157834409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567671569	chr3:157834422-157834423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs111902796	chr3:157834426-157834427	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537879541	chr3:157834431-157834432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556424724	chr3:157834442-157834443	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1333 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157828600-157845800	Weak transcription	Spleen	Spleen
2	chr3:157828600-157847800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:157828600-157857000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:157828800-157839600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr3:157828800-157840800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr3:157828800-157841200	Weak transcription	Left Ventricle	heart
7	chr3:157828800-157847600	Weak transcription	NH-A	brain
8	chr3:157828800-157851000	Weak transcription	Right Ventricle	heart
9	chr3:157829000-157840600	Weak transcription	Fetal Kidney	kidney
10	chr3:157829000-157840800	Weak transcription	Adipose Nuclei	Adipose
11	chr3:157829000-157841000	Weak transcription	Fetal Intestine Large	intestine
12	chr3:157829000-157841200	Weak transcription	Brain Hippocampus Middle	brain
13	chr3:157829000-157841400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr3:157829000-157849400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr3:157829200-157839600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:157829200-157840000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:157829200-157840600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr3:157829200-157840800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr3:157829200-157841200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr3:157829200-157841200	Weak transcription	Fetal Thymus	thymus
21	chr3:157829200-157841400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr3:157829200-157841800	Weak transcription	Brain Substantia Nigra	brain
23	chr3:157829200-157842000	Weak transcription	Psoas Muscle	Psoas
24	chr3:157829200-157845400	Weak transcription	HMEC	breast
25	chr3:157829200-157861400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr3:157829400-157839000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:157829400-157840600	Weak transcription	Fetal Lung	lung
28	chr3:157829600-157839600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:157829600-157840600	Weak transcription	Brain Anterior Caudate	brain
30	chr3:157829600-157840800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr3:157829600-157841400	Weak transcription	Primary B cells from cord blood	blood
32	chr3:157829800-157840800	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr3:157830000-157835200	Weak transcription	K562	blood
34	chr3:157830000-157835800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr3:157830000-157839200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr3:157830000-157840200	Weak transcription	Colon Smooth Muscle	Colon
37	chr3:157830000-157840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr3:157830000-157840600	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr3:157830000-157840600	Weak transcription	Thymus	Thymus
40	chr3:157830000-157840800	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr3:157830000-157841000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr3:157830000-157841200	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr3:157830000-157841200	Weak transcription	Hela-S3	cervix
44	chr3:157830000-157841400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:157830000-157841400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr3:157830000-157843400	Weak transcription	Small Intestine	intestine
47	chr3:157830000-157866400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr3:157830200-157840600	Weak transcription	Primary T cells from cord blood	blood
49	chr3:157830200-157840800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr3:157830200-157841400	Weak transcription	HepG2	liver

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