Variant report

Variant	nsv521469
Chromosome Location	chr8:124172895-124177926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:124172234..124173328-chr8:124232518..124233542,12	MCF-7	breast:
2	chr8:124172170..124173373-chr8:124203108..124203740,5	MCF-7	breast:
3	chr8:124164274..124174107-chr8:124177179..124181294,15	K562	blood:
4	chr8:124167743..124172035-chr8:124177154..124180052,5	MCF-7	breast:
5	chr8:124172665..124173321-chr8:124204596..124205175,2	MCF-7	breast:
6	chr8:124171738..124174563-chr8:124175786..124180198,3	MCF-7	breast:
7	chr8:124172440..124173389-chr8:124775729..124776620,2	MCF-7	breast:
8	chr8:124164381..124166664-chr8:124173510..124175947,2	K562	blood:
9	chr8:124173844..124174533-chr8:124232603..124233348,2	MCF-7	breast:
10	chr8:124166527..124173335-chr8:124188357..124196720,12	K562	blood:
11	chr8:124172180..124173617-chr8:124232329..124233727,43	MCF-7	breast:
12	chr8:124175599..124182947-chr8:124187251..124193031,13	K562	blood:
13	chr8:124172226..124173291-chr8:124203205..124204142,6	MCF-7	breast:
14	chr8:123796489..123798118-chr8:124177230..124179906,2	MCF-7	breast:
15	chr8:124174839..124177089-chr8:124178811..124181390,3	K562	blood:
16	chr8:124169245..124176335-chr8:124192965..124197106,7	MCF-7	breast:
17	chr8:124167900..124173832-chr8:124175566..124180994,14	K562	blood:
18	chr8:124164274..124174107-chr8:124177179..124181294,15	K562	blood:
19	chr8:124171396..124176501-chr8:124228974..124234727,7	MCF-7	breast:
20	chr8:124172763..124173313-chr8:124193922..124194776,2	MCF-7	breast:
21	chr8:123685508..123686390-chr8:124172412..124173006,2	MCF-7	breast:
22	chr10:62506708..62507282-chr8:124172451..124173316,2	MCF-7	breast:
23	chr8:124168721..124173901-chr8:124230598..124235089,6	MCF-7	breast:
24	chr8:124170086..124172909-chr8:124175029..124176545,2	MCF-7	breast:
25	chr8:124168117..124171297-chr8:124171831..124175255,6	K562	blood:
26	chr8:124053032..124054921-chr8:124170087..124173006,2	K562	blood:
27	chr8:124171432..124174128-chr8:124286899..124289260,2	MCF-7	breast:
28	chr8:124171361..124173486-chr8:124193492..124195637,4	MCF-7	breast:
29	chr8:124170086..124172909-chr8:124175029..124176545,2	MCF-7	breast:
30	chr3:64674543..64675446-chr8:124172470..124173272,2	MCF-7	breast:
31	chr8:124171651..124174347-chr8:124191271..124192791,2	MCF-7	breast:
32	chr8:124167900..124173832-chr8:124175566..124180994,14	K562	blood:
33	chr8:124171738..124174563-chr8:124175786..124180198,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000156787	chromatin interactions
ENSG00000253258	chromatin interactions
ENSG00000221461	chromatin interactions
ENSG00000165156	chromatin interactions
ENSG00000253410	chromatin interactions
ENSG00000136986	chromatin interactions
ENSG00000147689	chromatin interactions

Extended variants
information (count: 192 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:192 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16898060	chr8:124172895-124172896	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542767653	chr8:124172923-124172924	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs562535069	chr8:124172974-124172975	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs79340513	chr8:124172979-124172980	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs73339658	chr8:124173007-124173008	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs571123379	chr8:124173087-124173088	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs528027236	chr8:124173226-124173227	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs553116175	chr8:124173313-124173314	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs187677355	chr8:124173364-124173365	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs563282302	chr8:124173379-124173380	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs113265936	chr8:124173399-124173400	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs536216055	chr8:124173424-124173425	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs538717007	chr8:124173434-124173435	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs557176092	chr8:124173437-124173438	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs575550614	chr8:124173506-124173507	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs375297632	chr8:124173524-124173525	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs115697009	chr8:124173631-124173632	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs569770558	chr8:124173658-124173659	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs114063250	chr8:124173688-124173689	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs536288247	chr8:124173691-124173692	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs557975140	chr8:124173704-124173705	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs577748330	chr8:124173765-124173766	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs540550883	chr8:124173785-124173786	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs78613803	chr8:124173786-124173787	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs74513264	chr8:124173787-124173788	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs540816169	chr8:124173808-124173809	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs532118392	chr8:124173878-124173879	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs7827144	chr8:124173885-124173886	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs59033571	chr8:124173898-124173899	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs76055174	chr8:124173927-124173928	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs552180962	chr8:124173931-124173932	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs374306489	chr8:124173950-124173951	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs544767630	chr8:124173976-124173977	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs193210061	chr8:124173979-124173980	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs371102534	chr8:124174028-124174029	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs527857518	chr8:124174047-124174048	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs185506603	chr8:124174052-124174053	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs530740931	chr8:124174074-124174075	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs1670187	chr8:124174088-124174089	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs1670186	chr8:124174090-124174091	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs189233910	chr8:124174100-124174101	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs1670185	chr8:124174112-124174113	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs545042388	chr8:124174131-124174132	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs530042912	chr8:124174156-124174157	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs1670184	chr8:124174157-124174158	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs544515321	chr8:124174161-124174162	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs200967016	chr8:124174175-124174176	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs569707854	chr8:124174189-124174190	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs563248505	chr8:124174190-124174191	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs539159569	chr8:124174195-124174196	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:143)

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
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
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124170200-124173400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
2	chr8:124171000-124173000	Weak transcription	Small Intestine	intestine
3	chr8:124172400-124173200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
4	chr8:124172400-124173200	Active TSS	Brain Hippocampus Middle	brain
5	chr8:124172400-124173400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:124172400-124173400	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr8:124172400-124173400	Flanking Active TSS	Hela-S3	cervix
8	chr8:124172400-124173400	Flanking Active TSS	NHEK	skin
9	chr8:124172400-124173600	Enhancers	Fetal Brain Male	brain
10	chr8:124172400-124174000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
11	chr8:124172400-124174000	Active TSS	Brain Anterior Caudate	brain
12	chr8:124172600-124173000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr8:124172600-124173000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr8:124172600-124173000	Active TSS	Esophagus	oesophagus
15	chr8:124172600-124173200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:124172600-124173200	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr8:124172600-124173200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr8:124172600-124173200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr8:124172600-124173200	Active TSS	A549	lung
20	chr8:124172600-124173200	Flanking Bivalent TSS/Enh	Dnd41	blood
21	chr8:124172600-124173200	Active TSS	NH-A	brain
22	chr8:124172600-124173400	Active TSS	H1 Cell Line	embryonic stem cell
23	chr8:124172600-124173400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:124172600-124173400	Active TSS	Fetal Intestine Large	intestine
25	chr8:124172600-124173400	Flanking Active TSS	HMEC	breast
26	chr8:124172600-124173400	Active TSS	HSMM	muscle
27	chr8:124172600-124173600	Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr8:124172600-124173600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:124172600-124173600	Active TSS	Colon Smooth Muscle	Colon
30	chr8:124172600-124173800	Active TSS	H9 Cell Line	embryonic stem cell
31	chr8:124172600-124173800	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr8:124172600-124173800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr8:124172600-124173800	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr8:124172600-124173800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr8:124172600-124173800	Active TSS	Primary T cells from cord blood	blood
36	chr8:124172600-124173800	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr8:124172600-124173800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:124172600-124173800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:124172600-124173800	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr8:124172600-124173800	Active TSS	Brain Angular Gyrus	brain
41	chr8:124172600-124173800	Active TSS	Brain Cingulate Gyrus	brain
42	chr8:124172600-124173800	Active TSS	Brain Germinal Matrix	brain
43	chr8:124172600-124173800	Active TSS	Fetal Brain Female	brain
44	chr8:124172600-124173800	Active TSS	Fetal Kidney	kidney
45	chr8:124172600-124173800	Active TSS	Right Atrium	heart
46	chr8:124172600-124173800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr8:124172600-124173800	Active TSS	Thymus	Thymus
48	chr8:124172600-124174000	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr8:124172600-124174000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr8:124172600-124174000	Active TSS	Duodenum Smooth Muscle	Duodenum

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