Variant report

Variant	nsv528893
Chromosome Location	chr8:121914565-121928562
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	CEBPB	chr8:121927422-121927647	HepG2	liver:	n/a	chr8:121927540-121927551
2	CEBPB	chr8:121922085-121922118	HepG2	liver:	n/a	chr8:121922093-121922104
3	CHD2	chr8:121925116-121925316	HepG2	liver:	n/a	n/a
4	CHD2	chr8:121925177-121925333	GM12878	blood:	n/a	n/a
5	CTCF	chr8:121926160-121926310	HBMEC	blood vessel:	n/a	n/a
6	CTCF	chr8:121926300-121926450	BE2_C	brain:	n/a	n/a
7	CTCF	chr8:121926620-121926770	Caco-2	colon:	n/a	n/a
8	CTCF	chr8:121926660-121926810	NHEK	skin:	n/a	n/a
9	CTCF	chr8:121926120-121926270	HEK293	kidney:	n/a	n/a
10	CTCF	chr8:121919031-121919084	Fibrobl	skin:	n/a	n/a
11	FOS	chr8:121919082-121919421	MCF10A-Er-Src	breast:	n/a	chr8:121919228-121919238 chr8:121919228-121919238 chr8:121919228-121919237 chr8:121919228-121919238 chr8:121919215-121919224
12	FOS	chr8:121917033-121917238	MCF10A-Er-Src	breast:	n/a	chr8:121917154-121917163 chr8:121917154-121917161
13	FOS	chr8:121919085-121919421	MCF10A-Er-Src	breast:	n/a	chr8:121919228-121919238 chr8:121919228-121919238 chr8:121919228-121919237 chr8:121919228-121919238 chr8:121919215-121919224
14	FOS	chr8:121917006-121917300	MCF10A-Er-Src	breast:	n/a	chr8:121917154-121917163 chr8:121917154-121917161
15	FOS	chr8:121917034-121917293	MCF10A-Er-Src	breast:	n/a	chr8:121917154-121917163 chr8:121917154-121917161
16	FOS	chr8:121916990-121917337	MCF10A-Er-Src	breast:	n/a	chr8:121917154-121917163 chr8:121917154-121917161
17	FOS	chr8:121919107-121919411	MCF10A-Er-Src	breast:	n/a	chr8:121919228-121919238 chr8:121919228-121919238 chr8:121919228-121919237 chr8:121919228-121919238 chr8:121919215-121919224
18	FOS	chr8:121919086-121919434	MCF10A-Er-Src	breast:	n/a	chr8:121919228-121919238 chr8:121919228-121919238 chr8:121919228-121919237 chr8:121919228-121919238 chr8:121919215-121919224
19	FOXP2	chr8:121920645-121920992	SK-N-MC	brain:	n/a	n/a
20	IRF1	chr8:121920882-121921008	K562	blood:	n/a	n/a
21	JUN	chr8:121916788-121916854	H1-hESC	embryonic stem cell:	n/a	n/a
22	JUND	chr8:121919136-121919390	HepG2	liver:	n/a	chr8:121919227-121919238 chr8:121919228-121919238 chr8:121919228-121919238 chr8:121919228-121919237 chr8:121919228-121919238 chr8:121919215-121919224
23	JUND	chr8:121916960-121917292	HepG2	liver:	n/a	chr8:121917154-121917163 chr8:121917154-121917161 chr8:121917152-121917163
24	MAFF	chr8:121920645-121921071	HepG2	liver:	n/a	chr8:121920855-121920869 chr8:121920856-121920874
25	MAFF	chr8:121920675-121921047	K562	blood:	n/a	chr8:121920855-121920869 chr8:121920856-121920874
26	MAFK	chr8:121920660-121921051	HepG2	liver:	n/a	chr8:121920861-121920872 chr8:121920862-121920873 chr8:121920860-121920874 chr8:121920857-121920872 chr8:121920852-121920872 chr8:121920857-121920873 chr8:121920854-121920870 chr8:121920855-121920869 chr8:121920862-121920873 chr8:121920905-121920916
27	MAFK	chr8:121920672-121921050	HepG2	liver:	n/a	chr8:121920861-121920872 chr8:121920862-121920873 chr8:121920860-121920874 chr8:121920857-121920872 chr8:121920852-121920872 chr8:121920857-121920873 chr8:121920854-121920870 chr8:121920855-121920869 chr8:121920862-121920873 chr8:121920905-121920916
28	MAFK	chr8:121920675-121921049	K562	blood:	n/a	chr8:121920861-121920872 chr8:121920862-121920873 chr8:121920860-121920874 chr8:121920857-121920872 chr8:121920852-121920872 chr8:121920857-121920873 chr8:121920854-121920870 chr8:121920855-121920869 chr8:121920862-121920873 chr8:121920905-121920916
29	MAFK	chr8:121920674-121921048	H1-hESC	embryonic stem cell:	n/a	chr8:121920861-121920872 chr8:121920862-121920873 chr8:121920860-121920874 chr8:121920857-121920872 chr8:121920852-121920872 chr8:121920857-121920873 chr8:121920854-121920870 chr8:121920855-121920869 chr8:121920862-121920873 chr8:121920905-121920916
30	MAFK	chr8:121920501-121921067	GM12878	blood:	n/a	chr8:121920861-121920872 chr8:121920862-121920873 chr8:121920860-121920874 chr8:121920857-121920872 chr8:121920852-121920872 chr8:121920857-121920873 chr8:121920854-121920870 chr8:121920855-121920869 chr8:121920862-121920873 chr8:121920905-121920916
31	MAFK	chr8:121920666-121921061	IMR90	lung:	n/a	chr8:121920861-121920872 chr8:121920862-121920873 chr8:121920860-121920874 chr8:121920857-121920872 chr8:121920852-121920872 chr8:121920857-121920873 chr8:121920854-121920870 chr8:121920855-121920869 chr8:121920862-121920873 chr8:121920905-121920916
32	MAFK	chr8:121920675-121921080	Hela-S3	cervix:	n/a	chr8:121920861-121920872 chr8:121920862-121920873 chr8:121920860-121920874 chr8:121920857-121920872 chr8:121920852-121920872 chr8:121920857-121920873 chr8:121920854-121920870 chr8:121920855-121920869 chr8:121920862-121920873 chr8:121920905-121920916
33	MXI1	chr8:121926672-121926824	H1-hESC	embryonic stem cell:	n/a	chr8:121926696-121926705 chr8:121926698-121926707 chr8:121926696-121926705
34	MYC	chr8:121915418-121915543	H1-hESC	embryonic stem cell:	n/a	n/a
35	MYC	chr8:121919094-121919403	MCF10A-Er-Src	breast:	n/a	n/a
36	MYC	chr8:121928097-121928113	MCF10A-Er-Src	breast:	n/a	n/a
37	NFYB	chr8:121928207-121928767	GM12878	blood:	n/a	chr8:121928631-121928646 chr8:121928632-121928646 chr8:121928631-121928646 chr8:121928634-121928644
38	NFYB	chr8:121928441-121928782	K562	blood:	n/a	chr8:121928631-121928646 chr8:121928632-121928646 chr8:121928631-121928646 chr8:121928634-121928644
39	POLR2A	chr8:121919018-121919110	MCF-7	breast:	n/a	n/a
40	POLR2A	chr8:121927251-121927422	GM12878	blood:	n/a	n/a
41	POLR2A	chr8:121920599-121921059	SK-N-MC	brain:	n/a	n/a
42	SMC3	chr8:121926695-121926722	Hela-S3	cervix:	n/a	n/a
43	SPI1	chr8:121925189-121925757	HL-60	blood:	n/a	n/a
44	SPI1	chr8:121925331-121925593	HL-60	blood:	n/a	n/a
45	SPI1	chr8:121925456-121925600	GM12878	blood:	n/a	n/a
46	SPI1	chr8:121925398-121925690	GM12891	blood:	n/a	n/a
47	SPI1	chr8:121925423-121925588	K562	blood:	n/a	n/a
48	SPI1	chr8:121925410-121925612	K562	blood:	n/a	n/a
49	SPI1	chr8:121925103-121925810	GM12878	blood:	n/a	n/a
50	SPI1	chr8:121925378-121925680	GM12878	blood:	n/a	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTBP-2	chr8:121925305-121925399	ENSG00000253619

Variant related genes	Relation type
ENSG00000253619	TF binding region

Extended variants
information (count: 477 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564822192	chr8:121916849-121916850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs16894389	chr8:121916884-121916885	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs374154678	chr8:121916891-121916892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183181317	chr8:121916967-121916968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371370864	chr8:121916977-121916978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186044349	chr8:121917045-121917046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527946515	chr8:121917049-121917050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549189310	chr8:121917069-121917070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190345892	chr8:121917080-121917081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs80251067	chr8:121917101-121917102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183249128	chr8:121917133-121917134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149908564	chr8:121917154-121917155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571603095	chr8:121917177-121917178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539032414	chr8:121917180-121917181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187639886	chr8:121917217-121917218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs28650829	chr8:121917218-121917219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs144877540	chr8:121917231-121917232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191093061	chr8:121917368-121917369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79065348	chr8:121917371-121917372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117398818	chr8:121917382-121917383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558625194	chr8:121917384-121917385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576827252	chr8:121917385-121917386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541037478	chr8:121917396-121917397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548160974	chr8:121917414-121917415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148618501	chr8:121917419-121917420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542950150	chr8:121917425-121917426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182717472	chr8:121917449-121917450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201207655	chr8:121917504-121917505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531935726	chr8:121917508-121917509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550066706	chr8:121917510-121917511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113833829	chr8:121917518-121917519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532470391	chr8:121917532-121917533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147860283	chr8:121917544-121917545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187791485	chr8:121917559-121917560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568718365	chr8:121917581-121917582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10111219	chr8:121917652-121917653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs375909476	chr8:121917655-121917656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10096496	chr8:121917686-121917687	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs558432719	chr8:121917711-121917712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs80102600	chr8:121917758-121917759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192801389	chr8:121917764-121917765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552636590	chr8:121917817-121917818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141327882	chr8:121917853-121917854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74714246	chr8:121917939-121917940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369735954	chr8:121918004-121918005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561635453	chr8:121918043-121918044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12543462	chr8:121918155-121918156	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146973647	chr8:121918226-121918227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs28490321	chr8:121918231-121918232	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs574363767	chr8:121918240-121918241	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121916800-121917200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr8:121917200-121918200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr8:121918000-121920200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:121918200-121919400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr8:121918600-121919200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr8:121918600-121919600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr8:121918800-121919000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:121918800-121919200	Enhancers	HMEC	breast
9	chr8:121918800-121920000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:121918800-121920000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:121918800-121920000	Enhancers	HSMM	muscle
12	chr8:121919000-121919200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:121919000-121919200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:121919000-121919200	Enhancers	Psoas Muscle	Psoas
15	chr8:121919000-121919400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:121919000-121919400	Enhancers	Adipose Nuclei	Adipose
17	chr8:121919000-121919400	Bivalent Enhancer	NHDF-Ad	bronchial
18	chr8:121919000-121919400	Enhancers	Osteobl	bone
19	chr8:121919000-121919600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:121919000-121920000	Enhancers	HSMMtube	muscle
21	chr8:121919000-121920200	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr8:121919200-121919400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr8:121919200-121921600	Weak transcription	Psoas Muscle	Psoas
24	chr8:121919400-121919800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:121919400-121919800	Weak transcription	Adipose Nuclei	Adipose
26	chr8:121919800-121920400	Enhancers	Adipose Nuclei	Adipose
27	chr8:121919800-121920800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:121919800-121921000	Enhancers	Brain Germinal Matrix	brain
29	chr8:121920000-121926000	Weak transcription	HSMM	muscle
30	chr8:121920200-121922800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:121922800-121923000	Enhancers	Placenta	Placenta
32	chr8:121922800-121923200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:121922800-121923400	Enhancers	Fetal Thymus	thymus
34	chr8:121923200-121924600	Weak transcription	Placenta	Placenta
35	chr8:121923400-121926000	Weak transcription	Fetal Thymus	thymus
36	chr8:121924600-121926800	Enhancers	Placenta	Placenta
37	chr8:121924800-121925000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:121925000-121925200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:121925000-121925800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:121925200-121925400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:121925200-121925600	Enhancers	Primary B cells from peripheral blood	blood
42	chr8:121925400-121929000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:121925800-121926400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:121925800-121927400	Enhancers	HSMMtube	muscle
45	chr8:121925800-121928400	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr8:121926000-121927000	Enhancers	Fetal Muscle Leg	muscle
47	chr8:121926000-121927400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:121926000-121927600	Enhancers	HMEC	breast
49	chr8:121926000-121927600	Enhancers	HSMM	muscle
50	chr8:121926000-121928800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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