Variant report

Variant	nsv5705
Chromosome Location	chr7:38276267-38314121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:488)
Chromatin interactive
region (count:3)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

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	chr7:38298851-38299117	K562	blood:	n/a	n/a
3	ATF1	chr7:38278820-38279001	K562	blood:	n/a	n/a
4	ATF1	chr7:38285866-38286066	K562	blood:	n/a	n/a
5	ATF1	chr7:38285408-38285488	K562	blood:	n/a	n/a
6	ATF1	chr7:38296748-38296967	K562	blood:	n/a	n/a
7	ATF2	chr7:38289493-38289850	GM12878	blood:	n/a	n/a
8	BATF	chr7:38305659-38305874	GM12878	blood:	n/a	n/a
9	BATF	chr7:38289510-38289833	GM12878	blood:	n/a	n/a
10	BATF	chr7:38305616-38305913	GM12878	blood:	n/a	n/a
11	BATF	chr7:38289507-38289847	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38305548-38305926	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:38305612-38305832	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:38289442-38289823	GM12878	blood:	n/a	chr7:38289640-38289649
15	BCL11A	chr7:38289452-38289744	GM12878	blood:	n/a	chr7:38289640-38289649
16	BHLHE40	chr7:38313008-38313126	K562	blood:	n/a	n/a
17	CEBPB	chr7:38282958-38283308	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:38282957-38283329	A549	lung:	n/a	n/a
19	CEBPB	chr7:38282957-38283270	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:38282969-38283326	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:38282943-38283333	K562	blood:	n/a	n/a
22	CEBPB	chr7:38285344-38285395	K562	blood:	n/a	n/a
23	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
24	CEBPB	chr7:38312888-38313596	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:38282963-38283206	MCF-7	breast:	n/a	n/a
26	CEBPB	chr7:38282956-38283330	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:38282932-38283307	K562	blood:	n/a	chr7:38282939-38282951
28	CTCF	chr7:38280110-38280114	GM13977	blood:	n/a	n/a
29	CTCF	chr7:38279645-38279665	GM13976	blood:	n/a	n/a
30	CTCF	chr7:38280315-38280409	Fibrobl	skin:	n/a	n/a
31	CTCF	chr7:38299457-38299550	Lung_OC	lung:	n/a	n/a
32	CTCF	chr7:38292997-38293033	Lung_OC	lung:	n/a	n/a
33	CTCF	chr7:38298899-38298986	ProgFib	skin:	n/a	n/a
34	CTCF	chr7:38300410-38300476	Fibrobl	skin:	n/a	n/a
35	CTCF	chr7:38310342-38310394	Fibrobl	skin:	n/a	n/a
36	CTCF	chr7:38280053-38280101	GM13977	blood:	n/a	n/a
37	CTCF	chr7:38288542-38288588	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr7:38306007-38306040	MCF-7	breast:	n/a	n/a
39	E2F4	chr7:38295337-38295499	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr7:38277630-38277808	MCF10A-Er-Src	breast:	n/a	n/a
41	EP300	chr7:38296707-38296986	K562	blood:	n/a	n/a
42	EP300	chr7:38312905-38313623	MCF-7	breast:	n/a	n/a
43	FOS	chr7:38283120-38283200	MCF10A-Er-Src	breast:	n/a	n/a
44	FOXA1	chr7:38313205-38313498	T-47D	breast:	n/a	n/a
45	FOXA1	chr7:38304239-38304536	T-47D	breast:	n/a	n/a
46	FOXA1	chr7:38304288-38304517	T-47D	breast:	n/a	n/a
47	FOXA1	chr7:38313179-38313525	T-47D	breast:	n/a	n/a
48	FOXM1	chr7:38313033-38313534	MCF-7	breast:	n/a	n/a
49	FOXM1	chr7:38313122-38313587	MCF-7	breast:	n/a	n/a
50	GATA3	chr7:38311742-38312001	SH-SY5Y	brain:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38294113-38294163	SK-N-SH_RA	brain:	n/a
2	chr7:38299481-38299531	NH-A	brain:	n/a
3	chr7:38294113-38294163	NH-A	brain:	n/a
4	chr7:38296393-38296443	HEK293	kidney:	embryo
5	chr7:38298908-38298958	HEK293	kidney:	embryo
6	chr7:38294113-38294163	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:38299481-38299531	AG09309	skin:	n/a
8	chr7:38294113-38294163	GM06990	blood:	n/a
9	chr7:38294113-38294163	LNCaP	prostate:	n/a
10	chr7:38312366-38312416	ECC-1	luminal epithelium:	n/a
11	chr7:38294113-38294163	PrEC	prostate:	n/a
12	chr7:38309984-38310034	GM06990	blood:	n/a
13	chr7:38294113-38294163	CMK	blood:	n/a
14	chr7:38299481-38299531	Caco-2	colon:	n/a
15	chr7:38298966-38299016	HIPEpiC	eye:	n/a
16	chr7:38299481-38299531	NB4	blood:	n/a
17	chr7:38298966-38299016	HUVEC	blood vessel:	n/a
18	chr7:38303957-38304007	RPTEC	kidney:	n/a
19	chr7:38312366-38312416	HCPEpiC	choroid plexus:	n/a
20	chr7:38298966-38299016	PFSK-1	brain:	n/a
21	chr7:38303957-38304007	HAEpiC	amniotic membrane:	n/a
22	chr7:38303957-38304007	SK-N-SH_RA	brain:	n/a
23	chr7:38298966-38299016	MCF-7	breast:	n/a
24	chr7:38294113-38294163	Hela-S3	cervix:	n/a
25	chr7:38294113-38294163	HUVEC	blood vessel:	n/a
26	chr7:38309984-38310034	BE2_C	brain:	n/a
27	chr7:38309984-38310034	GM12878	blood:	n/a
28	chr7:38298966-38299016	HRE	kidney:	n/a
29	chr7:38296393-38296443	ECC-1	luminal epithelium:	n/a
30	chr7:38296393-38296443	HUVEC	blood vessel:	n/a
31	chr7:38298966-38299016	HL-60	blood:	n/a
32	chr7:38312366-38312416	PFSK-1	brain:	n/a
33	chr7:38296393-38296443	AG10803	skin:	n/a
34	chr7:38312366-38312416	Jurkat	blood:	n/a
35	chr7:38298966-38299016	AG04449	skin:	fetal
36	chr7:38312366-38312416	SK-N-SH	brain:	n/a
37	chr7:38303957-38304007	GM12892	blood:	n/a
38	chr7:38298966-38299016	NHDF-neo	bronchial:	n/a
39	chr7:38303957-38304007	HCF	heart:	n/a
40	chr7:38299481-38299531	RPTEC	kidney:	n/a
41	chr7:38303957-38304007	H1-hESC	embryonic stem cell:	embryo
42	chr7:38298908-38298958	Hela-S3	cervix:	n/a
43	chr7:38303957-38304007	NB4	blood:	n/a
44	chr7:38303957-38304007	HCT-116	colon:	n/a
45	chr7:38312366-38312416	IMR90	lung:	fetal
46	chr7:38312366-38312416	PANC-1	pancreas:	n/a
47	chr7:38294113-38294163	U87	brain:	n/a
48	chr7:38303957-38304007	NT2-D1	testis:	n/a
49	chr7:38299481-38299531	HRE	kidney:	n/a
50	chr7:38296393-38296443	AoSMC	blood vessel:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10118970..10119677-chr7:38276136..38276938,2	NB4	blood:
2	chr7:38309718..38312267-chr7:38320422..38323270,2	MCF-7	breast:
3	chr7:38301028..38303453-chr7:38304151..38306717,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120167
2	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
3	lnc-AMPH-9	chr7:38305937-38306406	ucscGeneNc_uc003tgl_1
4	lnc-AMPH-10	chr7:38310790-38310903	ucscGeneNc_uc003tgm_1
5	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120166
6	lnc-AMPH-10	chr7:38308874-38309749	ucscGeneNc_uc003tgm_1
7	lnc-AMPH-10	chr7:38310012-38310298	ucscGeneNc_uc003tgm_1
8	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120161
9	lnc-AMPH-10	chr7:38313188-38313242	NONHSAT120170
10	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120169
11	lnc-AMPH-10	chr7:38292981-38293028	NONHSAT120161
12	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167
13	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120170
14	lnc-AMPH-10	chr7:38292981-38293025	NONHSAT120162
15	lnc-AMPH-10	chr7:38313188-38313238	NONHSAT120169
16	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120162
17	lnc-AMPH-10	chr7:38293236-38293239	NONHSAT120162

No data

Variant related genes	Relation type
TRGC2	TF binding region
TRGC1	TF binding region
TRGJP	TF binding region
TRGJP2	TF binding region
TRGJ2	TF binding region
TRGJ1	TF binding region
TRGC2	CpG island
TRGC1	CpG island
TRGJP	CpG island
TRGJP2	CpG island
TRGJ2	CpG island
TRGJ1	CpG island
ENSG00000211689	chromatin interactions

Extended variants
information (count: 1966 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1966 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7800076	chr7:38276309-38276310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs544854015	chr7:38276335-38276336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116636558	chr7:38276377-38276378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530356919	chr7:38276460-38276461	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181283824	chr7:38276475-38276476	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566766553	chr7:38276507-38276508	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545415796	chr7:38276509-38276510	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs80166985	chr7:38276524-38276525	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568797420	chr7:38276526-38276527	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537460844	chr7:38276547-38276548	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576960300	chr7:38276548-38276549	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs56045043	chr7:38276595-38276596	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs185016583	chr7:38276642-38276643	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534122152	chr7:38276679-38276680	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141815781	chr7:38276685-38276686	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576965438	chr7:38276696-38276697	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539079475	chr7:38276706-38276707	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558796994	chr7:38276738-38276739	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147115220	chr7:38276755-38276756	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544260885	chr7:38276756-38276757	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540512300	chr7:38276781-38276782	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147712612	chr7:38276815-38276816	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574785230	chr7:38276827-38276828	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142553977	chr7:38276878-38276879	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191081100	chr7:38276923-38276924	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528847300	chr7:38276927-38276928	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532607191	chr7:38276967-38276968	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552216988	chr7:38276981-38276982	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562420428	chr7:38277020-38277021	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs143361456	chr7:38277042-38277043	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548199020	chr7:38277174-38277175	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148215093	chr7:38277187-38277188	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528081994	chr7:38277192-38277193	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs56847792	chr7:38277194-38277195	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs141230948	chr7:38277270-38277271	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570589631	chr7:38277273-38277274	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539276311	chr7:38277339-38277340	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556353666	chr7:38277370-38277371	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571200116	chr7:38277423-38277424	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59586846	chr7:38277426-38277427	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183718493	chr7:38277457-38277458	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537992069	chr7:38277488-38277489	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554543707	chr7:38277505-38277506	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540675268	chr7:38277546-38277547	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189061806	chr7:38277557-38277558	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533023205	chr7:38277572-38277573	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540485202	chr7:38277619-38277620	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560639265	chr7:38277737-38277738	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150285714	chr7:38277745-38277746	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546064051	chr7:38277786-38277787	Weak transcription Enhancers Genic enhancers Strong transcription	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:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38261600-38277200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:38271000-38278200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr7:38271400-38276800	Enhancers	Primary hematopoietic stem cells	blood
4	chr7:38272200-38276400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr7:38272600-38278200	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr7:38273000-38277200	Enhancers	Primary T cells fromperipheralblood	blood
7	chr7:38273000-38277800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:38273200-38276800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:38273600-38277000	Enhancers	Dnd41	blood
10	chr7:38273800-38282600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr7:38273800-38292200	Weak transcription	Thymus	Thymus
12	chr7:38273800-38305400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr7:38274400-38276400	Weak transcription	Primary T cells from cord blood	blood
14	chr7:38275400-38276400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr7:38275600-38276400	Weak transcription	Fetal Thymus	thymus
16	chr7:38276000-38277000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr7:38276000-38278800	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr7:38276000-38279000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr7:38276200-38276400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr7:38276200-38276800	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr7:38276200-38277600	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr7:38276200-38278000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:38276400-38276800	Enhancers	Primary T cells from cord blood	blood
24	chr7:38276400-38277000	Enhancers	Fetal Thymus	thymus
25	chr7:38276400-38277200	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr7:38276400-38279000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:38276800-38282800	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr7:38276800-38285800	Weak transcription	Primary T cells from cord blood	blood
29	chr7:38276800-38295600	Weak transcription	Primary hematopoietic stem cells	blood
30	chr7:38277000-38277200	Weak transcription	Dnd41	blood
31	chr7:38277000-38277400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:38277000-38277600	Genic enhancers	Fetal Thymus	thymus
33	chr7:38277000-38280400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr7:38277200-38277400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:38277200-38277400	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr7:38277200-38278800	Genic enhancers	Primary T cells fromperipheralblood	blood
37	chr7:38277200-38279200	Strong transcription	Dnd41	blood
38	chr7:38277400-38277600	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr7:38277600-38284200	Weak transcription	Fetal Thymus	thymus
40	chr7:38277600-38292600	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr7:38277600-38292600	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr7:38277800-38282800	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr7:38278000-38290800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr7:38278200-38282400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr7:38278200-38287600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:38278800-38280200	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr7:38278800-38280400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr7:38279000-38280200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr7:38279000-38280400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr7:38279200-38280000	Weak transcription	Dnd41	blood

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