Variant report

Variant	esv3512269
Chromosome Location	chr7:38279972-38299481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:90)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:90 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38298340-38298378	K562	blood:	n/a	n/a
2	ATF1	chr7:38296748-38296967	K562	blood:	n/a	n/a
3	ATF1	chr7:38285866-38286066	K562	blood:	n/a	n/a
4	ATF1	chr7:38298851-38299117	K562	blood:	n/a	n/a
5	ATF1	chr7:38285408-38285488	K562	blood:	n/a	n/a
6	ATF2	chr7:38289493-38289850	GM12878	blood:	n/a	n/a
7	BATF	chr7:38289507-38289847	GM12878	blood:	n/a	n/a
8	BATF	chr7:38289510-38289833	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:38289452-38289744	GM12878	blood:	n/a	chr7:38289640-38289649
10	BCL11A	chr7:38289442-38289823	GM12878	blood:	n/a	chr7:38289640-38289649
11	CEBPB	chr7:38282932-38283307	K562	blood:	n/a	chr7:38282939-38282951
12	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
13	CEBPB	chr7:38282957-38283270	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:38282956-38283330	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:38282963-38283206	MCF-7	breast:	n/a	n/a
16	CEBPB	chr7:38282958-38283308	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:38282969-38283326	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:38285344-38285395	K562	blood:	n/a	n/a
19	CEBPB	chr7:38282943-38283333	K562	blood:	n/a	n/a
20	CEBPB	chr7:38282957-38283329	A549	lung:	n/a	n/a
21	CTCF	chr7:38298899-38298986	ProgFib	skin:	n/a	n/a
22	CTCF	chr7:38292997-38293033	Lung_OC	lung:	n/a	n/a
23	CTCF	chr7:38280110-38280114	GM13977	blood:	n/a	n/a
24	CTCF	chr7:38299457-38299550	Lung_OC	lung:	n/a	n/a
25	CTCF	chr7:38280053-38280101	GM13977	blood:	n/a	n/a
26	CTCF	chr7:38288542-38288588	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr7:38280315-38280409	Fibrobl	skin:	n/a	n/a
28	E2F4	chr7:38295337-38295499	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr7:38296707-38296986	K562	blood:	n/a	n/a
30	FOS	chr7:38283120-38283200	MCF10A-Er-Src	breast:	n/a	n/a
31	GATA3	chr7:38295488-38295652	SH-SY5Y	brain:	n/a	n/a
32	IRF1	chr7:38295253-38295287	K562	blood:	n/a	n/a
33	IRF4	chr7:38289425-38289865	GM12878	blood:	n/a	n/a
34	IRF4	chr7:38289363-38289945	GM12878	blood:	n/a	n/a
35	JUND	chr7:38296695-38297059	K562	blood:	n/a	n/a
36	MAFF	chr7:38282947-38283201	K562	blood:	n/a	n/a
37	MAFF	chr7:38282987-38283208	HepG2	liver:	n/a	n/a
38	MAFK	chr7:38283013-38283216	IMR90	lung:	n/a	n/a
39	MAFK	chr7:38282973-38283227	HepG2	liver:	n/a	n/a
40	MAFK	chr7:38282926-38283126	K562	blood:	n/a	n/a
41	MAFK	chr7:38282955-38283216	HepG2	liver:	n/a	n/a
42	MAFK	chr7:38282954-38283133	Hela-S3	cervix:	n/a	n/a
43	MAX	chr7:38296352-38297047	NB4	blood:	n/a	n/a
44	MAX	chr7:38298232-38298389	NB4	blood:	n/a	n/a
45	MAX	chr7:38282983-38283292	NB4	blood:	n/a	n/a
46	MYC	chr7:38296645-38296965	NB4	blood:	n/a	n/a
47	MYC	chr7:38283076-38283297	NB4	blood:	n/a	n/a
48	MYC	chr7:38280345-38280397	MCF-7	breast:	n/a	n/a
49	MYC	chr7:38298360-38298420	NB4	blood:	n/a	n/a
50	NFYB	chr7:38287843-38288025	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38299481-38299531	NT2-D1	testis:	n/a
2	chr7:38298908-38298958	NHDF-neo	bronchial:	n/a
3	chr7:38298966-38299016	NHBE	bronchial:	n/a
4	chr7:38298908-38298958	HRPEpiC	eye:	n/a
5	chr7:38294113-38294163	PrEC	prostate:	n/a
6	chr7:38299481-38299531	MCF10A-Er-Src	breast:	n/a
7	chr7:38296393-38296443	Jurkat	blood:	n/a
8	chr7:38299481-38299531	AG04449	skin:	fetal
9	chr7:38299481-38299531	GM12878	blood:	n/a
10	chr7:38298908-38298958	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:38294113-38294163	HCF	heart:	n/a
12	chr7:38299481-38299531	K562	blood:	n/a
13	chr7:38296393-38296443	HRCEpiC	kidney:	n/a
14	chr7:38296393-38296443	PANC-1	pancreas:	n/a
15	chr7:38298908-38298958	Hela-S3	cervix:	n/a
16	chr7:38296393-38296443	HMEC	breast:	n/a
17	chr7:38296393-38296443	LNCaP	prostate:	n/a
18	chr7:38298908-38298958	HCT-116	colon:	n/a
19	chr7:38296393-38296443	CMK	blood:	n/a
20	chr7:38299481-38299531	HMEC	breast:	n/a
21	chr7:38298966-38299016	HL-60	blood:	n/a
22	chr7:38296393-38296443	HCF	heart:	n/a
23	chr7:38298908-38298958	NT2-D1	testis:	n/a
24	chr7:38296393-38296443	Hela-S3	cervix:	n/a
25	chr7:38299481-38299531	CMK	blood:	n/a
26	chr7:38296393-38296443	H1-hESC	embryonic stem cell:	embryo
27	chr7:38294113-38294163	AG10803	skin:	n/a
28	chr7:38298966-38299016	Caco-2	colon:	n/a
29	chr7:38296393-38296443	Caco-2	colon:	n/a
30	chr7:38299481-38299531	HCPEpiC	choroid plexus:	n/a
31	chr7:38296393-38296443	BJ	skin:	n/a
32	chr7:38296393-38296443	PFSK-1	brain:	n/a
33	chr7:38296393-38296443	Hepatocyte	liver:	n/a
34	chr7:38298966-38299016	SK-N-SH	brain:	n/a
35	chr7:38299481-38299531	HEEpiC	esophagus:	n/a
36	chr7:38298908-38298958	NHBE	bronchial:	n/a
37	chr7:38296393-38296443	NT2-D1	testis:	n/a
38	chr7:38298966-38299016	PANC-1	pancreas:	n/a
39	chr7:38299481-38299531	HRE	kidney:	n/a
40	chr7:38296393-38296443	HL-60	blood:	n/a
41	chr7:38299481-38299531	AG09309	skin:	n/a
42	chr7:38294113-38294163	HEK293	kidney:	embryo
43	chr7:38299481-38299531	T-47D	breast:	n/a
44	chr7:38299481-38299531	NH-A	brain:	n/a
45	chr7:38299481-38299531	BJ	skin:	n/a
46	chr7:38299481-38299531	SK-N-SH	brain:	n/a
47	chr7:38299481-38299531	MCF-7	breast:	n/a
48	chr7:38294113-38294163	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:38296393-38296443	RPTEC	kidney:	n/a
50	chr7:38296393-38296443	NHBE	bronchial:	n/a

No data

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120167
2	lnc-AMPH-10	chr7:38292981-38293025	NONHSAT120162
3	lnc-AMPH-10	chr7:38293236-38293239	NONHSAT120162
4	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
5	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167
6	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120162
7	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120166
8	lnc-AMPH-10	chr7:38292981-38293028	NONHSAT120161
9	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120161

No data

Variant related genes	Relation type
TRGC2	TF binding region
TRGJP2	TF binding region
TRGJ2	TF binding region
TRGC2	CpG island
TRGJP2	CpG island
TRGJ2	CpG island

Extended variants
information (count: 1050 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535244153	chr7:38280035-38280036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558097706	chr7:38280064-38280065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577653544	chr7:38280137-38280138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536788152	chr7:38280160-38280161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199515836	chr7:38280210-38280211	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2534600	chr7:38280224-38280225	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
7	rs200414365	chr7:38280227-38280228	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185407823	chr7:38280234-38280235	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35782020	chr7:38280249-38280250	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34721935	chr7:38280251-38280252	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35522718	chr7:38280257-38280258	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567594498	chr7:38280258-38280259	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542475759	chr7:38280282-38280283	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35216448	chr7:38280330-38280331	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35596985	chr7:38280384-38280385	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35268837	chr7:38280433-38280434	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs573082009	chr7:38280439-38280440	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372447251	chr7:38280458-38280459	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545172381	chr7:38280474-38280475	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564972322	chr7:38280498-38280499	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190603766	chr7:38280550-38280551	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149825077	chr7:38280558-38280559	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563633975	chr7:38280560-38280561	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529321397	chr7:38280602-38280603	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571607616	chr7:38280614-38280615	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559262329	chr7:38280638-38280639	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549672636	chr7:38280643-38280644	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566344646	chr7:38280644-38280645	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528819206	chr7:38280653-38280654	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375433962	chr7:38280707-38280708	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371496646	chr7:38280742-38280743	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571748827	chr7:38280743-38280744	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192686667	chr7:38280775-38280776	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528116390	chr7:38280805-38280806	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2109364	chr7:38280817-38280818	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs556651482	chr7:38280889-38280890	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145816914	chr7:38280930-38280931	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148837491	chr7:38280950-38280951	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34348430	chr7:38280953-38280954	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566050819	chr7:38280958-38280959	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184257348	chr7:38280965-38280966	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189068618	chr7:38280970-38280971	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573081556	chr7:38281034-38281035	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372848429	chr7:38281038-38281039	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113411989	chr7:38281152-38281153	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545450746	chr7:38281154-38281155	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558672416	chr7:38281182-38281183	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111961381	chr7:38281215-38281216	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143508667	chr7:38281292-38281293	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185546809	chr7:38281308-38281309	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Multiple sclerosis	20428171	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Neuroblastoma	19536264	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38273800-38282600	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr7:38273800-38292200	Weak transcription	Thymus	Thymus
3	chr7:38273800-38305400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:38276800-38282800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr7:38276800-38285800	Weak transcription	Primary T cells from cord blood	blood
6	chr7:38276800-38295600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr7:38277000-38280400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:38277600-38284200	Weak transcription	Fetal Thymus	thymus
9	chr7:38277600-38292600	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr7:38277600-38292600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr7:38277800-38282800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr7:38278000-38290800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:38278200-38282400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr7:38278200-38287600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr7:38278800-38280200	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr7:38278800-38280400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr7:38279000-38280200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:38279000-38280400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr7:38279200-38280000	Weak transcription	Dnd41	blood
20	chr7:38280000-38281000	Strong transcription	Dnd41	blood
21	chr7:38280200-38281400	Genic enhancers	Primary T cells fromperipheralblood	blood
22	chr7:38280200-38281600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:38280400-38280600	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr7:38280400-38280800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr7:38280400-38281200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:38280600-38282600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:38280800-38284000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr7:38281000-38282000	Weak transcription	Dnd41	blood
29	chr7:38281200-38287200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr7:38281400-38281800	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:38281600-38282400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr7:38281800-38284000	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr7:38282000-38283000	Strong transcription	Dnd41	blood
34	chr7:38282400-38282800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:38282400-38283200	Strong transcription	Primary T killer memory cells from peripheral blood	blood
36	chr7:38282600-38282800	Bivalent Enhancer	K562	blood
37	chr7:38282600-38283200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:38282600-38283200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr7:38282600-38283600	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr7:38282800-38283000	Enhancers	K562	blood
41	chr7:38282800-38283000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr7:38282800-38283400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr7:38282800-38284200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:38283000-38283200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr7:38283000-38283800	Weak transcription	Dnd41	blood
46	chr7:38283000-38284400	Weak transcription	K562	blood
47	chr7:38283200-38283600	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr7:38283200-38285400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr7:38283200-38287800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr7:38283400-38286800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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