Variant report

Variant	nsv876624
Chromosome Location	chr3:23385877-23483536
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:373)
CpG islands
(count:183)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:23472393-23472877	GM12878	blood:	n/a	n/a
2	BATF	chr3:23463964-23464237	GM12878	blood:	n/a	n/a
3	BATF	chr3:23480155-23480444	GM12878	blood:	n/a	n/a
4	BATF	chr3:23480171-23480448	GM12878	blood:	n/a	n/a
5	BATF	chr3:23436607-23436931	GM12878	blood:	n/a	chr3:23436755-23436764
6	BCLAF1	chr3:23463910-23464435	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:23446575-23446933	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:23429181-23429214	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:23445745-23446118	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:23445735-23446103	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:23466021-23466291	IMR90	lung:	n/a	n/a
12	CEBPB	chr3:23438341-23438541	HepG2	liver:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
13	CEBPB	chr3:23404659-23405168	HepG2	liver:	n/a	chr3:23404763-23404774
14	CEBPB	chr3:23397764-23397950	HepG2	liver:	n/a	chr3:23397809-23397820
15	CEBPB	chr3:23454462-23454480	HepG2	liver:	n/a	n/a
16	CEBPB	chr3:23404746-23404806	Hela-S3	cervix:	n/a	chr3:23404763-23404774
17	CEBPB	chr3:23474391-23474588	HepG2	liver:	n/a	chr3:23474444-23474455
18	CEBPB	chr3:23438328-23438606	Hela-S3	cervix:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
19	CEBPB	chr3:23425510-23425634	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:23466068-23466225	A549	lung:	n/a	n/a
21	CEBPB	chr3:23466027-23466260	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:23397720-23397889	Hela-S3	cervix:	n/a	chr3:23397809-23397820
23	CEBPB	chr3:23438342-23438564	A549	lung:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
24	CEBPB	chr3:23474439-23474469	K562	blood:	n/a	chr3:23474444-23474455
25	CEBPB	chr3:23404653-23405172	IMR90	lung:	n/a	chr3:23404763-23404774
26	CEBPB	chr3:23404642-23405196	A549	lung:	n/a	chr3:23404763-23404774
27	CHD1	chr3:23446784-23446957	GM12878	blood:	n/a	n/a
28	CHD2	chr3:23429199-23429204	GM12878	blood:	n/a	n/a
29	CHD2	chr3:23472562-23472714	GM12878	blood:	n/a	n/a
30	CTCF	chr3:23413860-23414010	HVMF	connective:	n/a	n/a
31	CTCF	chr3:23413900-23414050	HCFaa	heart:	n/a	n/a
32	CTCF	chr3:23476920-23477070	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr3:23413860-23414010	GM12873	blood:	n/a	n/a
34	CTCF	chr3:23432114-23432127	ProgFib	skin:	n/a	n/a
35	CTCF	chr3:23477000-23477150	GM12873	blood:	n/a	n/a
36	CTCF	chr3:23413980-23414130	HCM	heart:	n/a	n/a
37	CTCF	chr3:23412160-23412310	HMEC	breast:	n/a	n/a
38	CTCF	chr3:23412200-23412350	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:23412080-23412230	HFF	foreskin:	n/a	n/a
40	CTCF	chr3:23413860-23414010	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr3:23412216-23412270	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr3:23413820-23413970	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr3:23413920-23414070	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:23412100-23412250	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr3:23412040-23412190	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:23412142-23412277	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:23412240-23412390	HCFaa	heart:	n/a	n/a
48	CTCF	chr3:23412080-23412230	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr3:23413860-23414010	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr3:23413860-23414010	HCPEpiC	choroid plexus:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23478304-23478354	HCF	heart:	n/a
2	chr3:23415040-23415090	AG09319	gingival:	n/a
3	chr3:23478304-23478354	T-47D	breast:	n/a
4	chr3:23415040-23415090	AG04449	skin:	fetal
5	chr3:23415040-23415090	HUVEC	blood vessel:	n/a
6	chr3:23448023-23448073	A549	lung:	n/a
7	chr3:23478304-23478354	U87	brain:	n/a
8	chr3:23478304-23478354	MCF10A-Er-Src	breast:	n/a
9	chr3:23448023-23448073	HRE	kidney:	n/a
10	chr3:23448023-23448073	HCF	heart:	n/a
11	chr3:23478304-23478354	HRE	kidney:	n/a
12	chr3:23415040-23415090	A549	lung:	n/a
13	chr3:23415040-23415090	HepG2	liver:	n/a
14	chr3:23448023-23448073	SKMC	muscle:	n/a
15	chr3:23415040-23415090	K562	blood:	n/a
16	chr3:23448023-23448073	NHBE	bronchial:	n/a
17	chr3:23415040-23415090	RPTEC	kidney:	n/a
18	chr3:23448023-23448073	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:23478304-23478354	NT2-D1	testis:	n/a
20	chr3:23415040-23415090	HRE	kidney:	n/a
21	chr3:23478304-23478354	HUVEC	blood vessel:	n/a
22	chr3:23415040-23415090	HIPEpiC	eye:	n/a
23	chr3:23415040-23415090	GM06990	blood:	n/a
24	chr3:23448023-23448073	SK-N-SH_RA	brain:	n/a
25	chr3:23448023-23448073	GM12892	blood:	n/a
26	chr3:23448023-23448073	HMEC	breast:	n/a
27	chr3:23478304-23478354	HMEC	breast:	n/a
28	chr3:23478304-23478354	PANC-1	pancreas:	n/a
29	chr3:23448023-23448073	MCF-7	breast:	n/a
30	chr3:23448023-23448073	HRCEpiC	kidney:	n/a
31	chr3:23415040-23415090	CMK	blood:	n/a
32	chr3:23415040-23415090	NT2-D1	testis:	n/a
33	chr3:23415040-23415090	HAEpiC	amniotic membrane:	n/a
34	chr3:23448023-23448073	AG10803	skin:	n/a
35	chr3:23448023-23448073	NH-A	brain:	n/a
36	chr3:23478304-23478354	H1-hESC	embryonic stem cell:	embryo
37	chr3:23415040-23415090	ovcar-3	ovarian:	n/a
38	chr3:23448023-23448073	HNPCEpiC	eye:	n/a
39	chr3:23478304-23478354	HEEpiC	esophagus:	n/a
40	chr3:23448023-23448073	HAEpiC	amniotic membrane:	n/a
41	chr3:23478304-23478354	GM12891	blood:	n/a
42	chr3:23448023-23448073	RPTEC	kidney:	n/a
43	chr3:23415040-23415090	Hela-S3	cervix:	n/a
44	chr3:23448023-23448073	HCM	heart:	n/a
45	chr3:23448023-23448073	ovcar-3	ovarian:	n/a
46	chr3:23448023-23448073	HCPEpiC	choroid plexus:	n/a
47	chr3:23448023-23448073	NHDF-neo	bronchial:	n/a
48	chr3:23478304-23478354	SAEC	small airway:	n/a
49	chr3:23478304-23478354	RPTEC	kidney:	n/a
50	chr3:23448023-23448073	Hela-S3	cervix:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
2	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
3	chr3:23482059..23483566-chr3:23484032..23486053,2	MCF-7	breast:
4	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
5	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
6	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
7	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
8	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
9	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
10	chr3:23477379..23479456-chr3:23479836..23482736,2	MCF-7	breast:
11	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
12	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:
13	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
14	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
15	chr3:23477632..23480027-chr3:23493781..23495810,2	MCF-7	breast:
16	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
17	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
18	chr3:23436579..23438931-chr3:23441202..23443899,2	K562	blood:
19	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
20	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
21	chr3:23477379..23479456-chr3:23479836..23482736,2	MCF-7	breast:
22	chr3:23478332..23479926-chr3:23487725..23489400,2	MCF-7	breast:
23	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
24	chr3:23436579..23438931-chr3:23441202..23443899,2	K562	blood:
25	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKIRAS1-5	chr3:23431152-23431400	NONHSAT088668

No data

Variant related genes	Relation type
ENSG00000221506	TF binding region
ENSG00000228171	TF binding region
ENSG00000221506	CpG island
ENSG00000228171	CpG island

Extended variants
information (count: 4021 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4021 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13076527	chr3:23385877-23385878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187054933	chr3:23385881-23385882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560771284	chr3:23385893-23385894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189903375	chr3:23385913-23385914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527679847	chr3:23385934-23385935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1054048	chr3:23385941-23385942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs17013049	chr3:23385942-23385943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs201484751	chr3:23385950-23385951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532006870	chr3:23386006-23386007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377014169	chr3:23386018-23386019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550417889	chr3:23386025-23386026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142401229	chr3:23386031-23386032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370055873	chr3:23386040-23386041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146792204	chr3:23386074-23386075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558809578	chr3:23386084-23386085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548331227	chr3:23386140-23386141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74922504	chr3:23386144-23386145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572199365	chr3:23386145-23386146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369673952	chr3:23386152-23386153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201108043	chr3:23386163-23386164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536255180	chr3:23386170-23386171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79952377	chr3:23386175-23386176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575955655	chr3:23386182-23386183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554232828	chr3:23386191-23386192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145167911	chr3:23386192-23386193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374274629	chr3:23386193-23386194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558367274	chr3:23386216-23386217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148360148	chr3:23386295-23386296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78238263	chr3:23386296-23386297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373664715	chr3:23386308-23386309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369465872	chr3:23386313-23386314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560635162	chr3:23386349-23386350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140386211	chr3:23386371-23386372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs61356176	chr3:23386373-23386374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182546204	chr3:23386392-23386393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199853898	chr3:23386393-23386394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539219226	chr3:23386394-23386395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543022053	chr3:23386460-23386461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561238257	chr3:23386483-23386484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187159046	chr3:23386506-23386507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140540260	chr3:23386538-23386539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150495715	chr3:23386539-23386540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34732257	chr3:23386571-23386572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138322814	chr3:23386579-23386580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377242544	chr3:23386616-23386617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547635479	chr3:23386692-23386693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113333797	chr3:23386729-23386730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182327201	chr3:23386792-23386793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568146256	chr3:23386828-23386829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185167990	chr3:23386847-23386848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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

Chromatin state (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23367400-23391400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:23368000-23391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:23380800-23389400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr3:23383000-23386000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr3:23384000-23389600	Weak transcription	GM12878-XiMat	blood
6	chr3:23384400-23391800	Weak transcription	Primary B cells from cord blood	blood
7	chr3:23384600-23390600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr3:23386600-23403800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr3:23388800-23390600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:23389400-23391000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr3:23390000-23390800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
12	chr3:23390200-23390600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr3:23390200-23391200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr3:23390400-23390800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
15	chr3:23390400-23391000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr3:23390400-23391200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
17	chr3:23390400-23391200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:23390600-23391200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr3:23390600-23391200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:23390600-23391200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr3:23390600-23391200	Enhancers	Primary B cells from peripheral blood	blood
22	chr3:23390800-23391200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr3:23391200-23395000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr3:23397400-23398400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:23397600-23398000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr3:23397600-23398000	Enhancers	Liver	Liver
27	chr3:23398200-23398600	Enhancers	Adipose Nuclei	Adipose
28	chr3:23398400-23398600	Enhancers	Psoas Muscle	Psoas
29	chr3:23398400-23413000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:23398600-23414600	Weak transcription	Psoas Muscle	Psoas
31	chr3:23399600-23399800	Enhancers	Brain Cingulate Gyrus	brain
32	chr3:23399800-23400800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr3:23400200-23401600	Enhancers	Brain Substantia Nigra	brain
34	chr3:23400800-23401800	Enhancers	Brain Cingulate Gyrus	brain
35	chr3:23403800-23404200	Enhancers	Gastric	stomach
36	chr3:23403800-23404200	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr3:23403800-23404400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr3:23404000-23404400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:23404200-23418000	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr3:23404400-23418000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr3:23406000-23407200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr3:23406200-23406600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:23406400-23407200	Enhancers	HUVEC	blood vessel
44	chr3:23406600-23407000	Enhancers	Primary B cells from peripheral blood	blood
45	chr3:23407000-23411000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr3:23408800-23409600	Enhancers	GM12878-XiMat	blood
47	chr3:23409000-23409200	ZNF genes & repeats	Aorta	Aorta
48	chr3:23409000-23409400	Enhancers	Spleen	Spleen
49	chr3:23409200-23431800	Weak transcription	Aorta	Aorta
50	chr3:23409600-23411400	Weak transcription	GM12878-XiMat	blood

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