Variant report

Variant	nsv589948
Chromosome Location	chr3:23287141-23390221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:183)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:23367105-23367549	GM12878	blood:	n/a	n/a
2	ATF2	chr3:23367108-23367548	GM12878	blood:	n/a	n/a
3	ATF2	chr3:23382835-23383365	GM12878	blood:	n/a	n/a
4	BACH1	chr3:23299743-23299785	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:23367094-23367570	GM12878	blood:	n/a	n/a
6	BATF	chr3:23298327-23298695	GM12878	blood:	n/a	n/a
7	BATF	chr3:23313878-23314156	GM12878	blood:	n/a	n/a
8	BATF	chr3:23367272-23367502	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:23367192-23367517	GM12878	blood:	n/a	n/a
10	BCL3	chr3:23367262-23367545	GM12878	blood:	n/a	n/a
11	BCLAF1	chr3:23367134-23367570	GM12878	blood:	n/a	n/a
12	CCNT2	chr3:23330795-23330876	K562	blood:	n/a	n/a
13	CEBPB	chr3:23319866-23320309	IMR90	lung:	n/a	n/a
14	CEBPB	chr3:23320037-23320201	A549	lung:	n/a	n/a
15	CEBPB	chr3:23320082-23320198	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:23356948-23357212	IMR90	lung:	n/a	n/a
17	CEBPB	chr3:23320068-23320261	K562	blood:	n/a	n/a
18	CEBPB	chr3:23314983-23315065	A549	lung:	n/a	n/a
19	CEBPB	chr3:23313998-23314235	IMR90	lung:	n/a	chr3:23314083-23314094 chr3:23314083-23314096 chr3:23314083-23314094
20	CHD1	chr3:23366250-23366294	GM12878	blood:	n/a	n/a
21	CTCF	chr3:23352117-23352135	Fibrobl	skin:	n/a	n/a
22	CTCF	chr3:23334080-23334230	K562	blood:	n/a	n/a
23	CTCF	chr3:23357320-23357470	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr3:23361480-23361630	GM12873	blood:	n/a	n/a
25	CTCF	chr3:23300170-23300219	GM13977	blood:	n/a	n/a
26	CTCF	chr3:23323040-23323095	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:23377900-23378050	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr3:23361340-23361490	MCF-7	breast:	n/a	n/a
29	CTCF	chr3:23378220-23378370	AG10803	skin:	n/a	n/a
30	CTCF	chr3:23313540-23313690	K562	blood:	n/a	n/a
31	CTCF	chr3:23361360-23361510	GM12864	blood:	n/a	n/a
32	CTCF	chr3:23313400-23313550	K562	blood:	n/a	n/a
33	CTCF	chr3:23312883-23312925	Medullo	brain:	n/a	n/a
34	CUX1	chr3:23367168-23367492	GM12878	blood:	n/a	n/a
35	CUX1	chr3:23336383-23336531	GM12878	blood:	n/a	n/a
36	CUX1	chr3:23330817-23331015	GM12878	blood:	n/a	n/a
37	CUX1	chr3:23366073-23366192	GM12878	blood:	n/a	n/a
38	CUX1	chr3:23380940-23380983	GM12878	blood:	n/a	n/a
39	CUX1	chr3:23382992-23383441	GM12878	blood:	n/a	n/a
40	E2F4	chr3:23366348-23366640	MCF10A-Er-Src	breast:	n/a	chr3:23366606-23366615 chr3:23366493-23366508
41	E2F4	chr3:23305378-23306024	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr3:23363405-23363605	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr3:23296276-23296428	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr3:23319346-23319543	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr3:23377670-23377838	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr3:23345294-23345464	GM12878	blood:	n/a	chr3:23345382-23345393
47	EBF1	chr3:23367154-23367472	GM12878	blood:	n/a	n/a
48	EBF1	chr3:23295828-23296200	GM12878	blood:	n/a	chr3:23295997-23296008
49	EBF1	chr3:23294809-23295007	GM12878	blood:	n/a	n/a
50	EBF1	chr3:23295882-23296066	GM12878	blood:	n/a	chr3:23295997-23296008

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23305946-23305996	Caco-2	colon:	n/a
2	chr3:23305946-23305996	HUVEC	blood vessel:	n/a
3	chr3:23305946-23305996	PANC-1	pancreas:	n/a
4	chr3:23305946-23305996	HCM	heart:	n/a
5	chr3:23313729-23313779	AG04450	lung:	fetal
6	chr3:23313729-23313779	NH-A	brain:	n/a
7	chr3:23313729-23313779	NB4	blood:	n/a
8	chr3:23331228-23331278	HCPEpiC	choroid plexus:	n/a
9	chr3:23313729-23313779	HCPEpiC	choroid plexus:	n/a
10	chr3:23331228-23331278	AG04449	skin:	fetal
11	chr3:23331228-23331278	SAEC	small airway:	n/a
12	chr3:23331228-23331278	Caco-2	colon:	n/a
13	chr3:23305946-23305996	U87	brain:	n/a
14	chr3:23305946-23305996	HMEC	breast:	n/a
15	chr3:23331228-23331278	AoSMC	blood vessel:	n/a
16	chr3:23313729-23313779	Jurkat	blood:	n/a
17	chr3:23305946-23305996	LNCaP	prostate:	n/a
18	chr3:23305946-23305996	ECC-1	luminal epithelium:	n/a
19	chr3:23313729-23313779	HCT-116	colon:	n/a
20	chr3:23331228-23331278	HRE	kidney:	n/a
21	chr3:23305946-23305996	IMR90	lung:	fetal
22	chr3:23305946-23305996	BJ	skin:	n/a
23	chr3:23305946-23305996	AG10803	skin:	n/a
24	chr3:23331228-23331278	NB4	blood:	n/a
25	chr3:23305946-23305996	HAEpiC	amniotic membrane:	n/a
26	chr3:23305946-23305996	PFSK-1	brain:	n/a
27	chr3:23331228-23331278	SK-N-SH_RA	brain:	n/a
28	chr3:23331228-23331278	Hepatocyte	liver:	n/a
29	chr3:23305946-23305996	T-47D	breast:	n/a
30	chr3:23313729-23313779	HCF	heart:	n/a
31	chr3:23331228-23331278	Hela-S3	cervix:	n/a
32	chr3:23331228-23331278	NT2-D1	testis:	n/a
33	chr3:23305946-23305996	Jurkat	blood:	n/a
34	chr3:23313729-23313779	AG09319	gingival:	n/a
35	chr3:23331228-23331278	SK-N-MC	brain:	n/a
36	chr3:23331228-23331278	HCF	heart:	n/a
37	chr3:23313729-23313779	HEK293	kidney:	embryo
38	chr3:23313729-23313779	NHDF-neo	bronchial:	n/a
39	chr3:23305946-23305996	ovcar-3	ovarian:	n/a
40	chr3:23313729-23313779	H1-hESC	embryonic stem cell:	embryo
41	chr3:23331228-23331278	RPTEC	kidney:	n/a
42	chr3:23331228-23331278	AG10803	skin:	n/a
43	chr3:23331228-23331278	PrEC	prostate:	n/a
44	chr3:23313729-23313779	GM12891	blood:	n/a
45	chr3:23305946-23305996	NB4	blood:	n/a
46	chr3:23305946-23305996	HCF	heart:	n/a
47	chr3:23331228-23331278	K562	blood:	n/a
48	chr3:23331228-23331278	GM12878	blood:	n/a
49	chr3:23305946-23305996	RPTEC	kidney:	n/a
50	chr3:23313729-23313779	K562	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
2	chr3:23361011..23363823-chr3:23364424..23367156,3	MCF-7	breast:
3	chr3:23333702..23336217-chr3:23346722..23349222,2	MCF-7	breast:
4	chr3:23360954..23362532-chr3:23363082..23365861,2	MCF-7	breast:
5	chr3:23245352..23245950-chr3:23374735..23375546,2	MCF-7	breast:
6	chr3:23360954..23362532-chr3:23363082..23365861,2	MCF-7	breast:
7	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:
8	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
9	chr3:23333702..23336217-chr3:23346722..23349222,2	MCF-7	breast:
10	chr3:23361011..23363823-chr3:23364424..23367156,3	MCF-7	breast:
11	chr3:23375136..23376980-chr3:23383143..23385276,2	MCF-7	breast:
12	chr3:23375136..23376980-chr3:23383143..23385276,2	MCF-7	breast:
13	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000206728	TF binding region
ENSG00000206728	CpG island

Extended variants
information (count: 4393 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4393 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17342904	chr3:23287141-23287142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561967679	chr3:23287162-23287163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571693597	chr3:23287175-23287176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147653868	chr3:23287233-23287234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554224057	chr3:23287237-23287238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17402378	chr3:23287243-23287244	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs191730991	chr3:23287262-23287263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555263401	chr3:23287267-23287268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572641352	chr3:23287295-23287296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140602254	chr3:23287312-23287313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34239585	chr3:23287321-23287322	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs75894752	chr3:23287322-23287323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576854097	chr3:23287360-23287361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184015733	chr3:23287364-23287365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548145609	chr3:23287377-23287378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558942518	chr3:23287384-23287385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151236396	chr3:23287438-23287439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541730433	chr3:23287490-23287491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563588211	chr3:23287523-23287524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530647809	chr3:23287551-23287552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35743404	chr3:23287570-23287571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564093633	chr3:23287611-23287612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189005031	chr3:23287625-23287626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140511173	chr3:23287669-23287670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4858485	chr3:23287706-23287707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs62255296	chr3:23287711-23287712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546770574	chr3:23287713-23287714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536641241	chr3:23287728-23287729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548649582	chr3:23287773-23287774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570305279	chr3:23287776-23287777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537279542	chr3:23287812-23287813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559118993	chr3:23287852-23287853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577335586	chr3:23287856-23287857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534415154	chr3:23287857-23287858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370057807	chr3:23287860-23287861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35802594	chr3:23287878-23287879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552609997	chr3:23287888-23287889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs71620770	chr3:23287899-23287900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370671736	chr3:23287900-23287901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71317818	chr3:23287912-23287913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11920019	chr3:23287914-23287915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541420740	chr3:23287932-23287933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563470483	chr3:23287933-23287934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111851708	chr3:23287968-23287969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545751588	chr3:23288005-23288006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564308241	chr3:23288006-23288007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528258016	chr3:23288021-23288022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547954018	chr3:23288039-23288040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559885273	chr3:23288044-23288045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562455061	chr3:23288150-23288151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1025 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23274800-23298200	Weak transcription	Aorta	Aorta
2	chr3:23278600-23289600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:23280200-23291400	Weak transcription	Psoas Muscle	Psoas
4	chr3:23280400-23290600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr3:23281400-23298200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr3:23282000-23290200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr3:23282200-23289000	Weak transcription	Adipose Nuclei	Adipose
8	chr3:23282200-23294600	Weak transcription	A549	lung
9	chr3:23283200-23296000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr3:23283600-23302200	Weak transcription	Left Ventricle	heart
11	chr3:23283800-23292000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr3:23285000-23290000	Weak transcription	Brain Cingulate Gyrus	brain
13	chr3:23285000-23292400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:23286400-23289600	Weak transcription	Brain Angular Gyrus	brain
15	chr3:23286600-23289000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:23286600-23289600	Weak transcription	Brain Substantia Nigra	brain
17	chr3:23286800-23289400	Weak transcription	Brain Anterior Caudate	brain
18	chr3:23286800-23289600	Weak transcription	Brain Hippocampus Middle	brain
19	chr3:23287600-23288200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:23288200-23288600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:23288600-23289200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:23288600-23289800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr3:23289000-23289600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:23289000-23290400	Enhancers	Adipose Nuclei	Adipose
25	chr3:23289000-23294800	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr3:23289200-23289800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:23289200-23292400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:23289400-23290400	Enhancers	Brain Anterior Caudate	brain
29	chr3:23289600-23289800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr3:23289600-23289800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr3:23289600-23290000	Enhancers	Brain Angular Gyrus	brain
32	chr3:23289600-23290400	Enhancers	Brain Hippocampus Middle	brain
33	chr3:23289600-23290600	Enhancers	Brain Substantia Nigra	brain
34	chr3:23290000-23290200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr3:23290000-23290600	Enhancers	Brain Cingulate Gyrus	brain
36	chr3:23290000-23292600	Weak transcription	Brain Angular Gyrus	brain
37	chr3:23290200-23290600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr3:23290400-23292400	Weak transcription	Brain Anterior Caudate	brain
39	chr3:23290400-23292400	Weak transcription	Brain Hippocampus Middle	brain
40	chr3:23290400-23295800	Weak transcription	Adipose Nuclei	Adipose
41	chr3:23290600-23290800	Enhancers	Primary B cells from peripheral blood	blood
42	chr3:23290600-23291800	Weak transcription	Brain Substantia Nigra	brain
43	chr3:23290600-23292400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr3:23290600-23298200	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr3:23290800-23294800	Weak transcription	Primary B cells from peripheral blood	blood
46	chr3:23291400-23291600	Enhancers	Spleen	Spleen
47	chr3:23291400-23291800	Enhancers	Thymus	Thymus
48	chr3:23291400-23292000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr3:23291400-23292000	Enhancers	Psoas Muscle	Psoas
50	chr3:23291400-23292200	Enhancers	Primary T cells from cord blood	blood

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