Variant report

Variant	nsv981557
Chromosome Location	chr7:99808038-99811640
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:173)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:173 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:99808755-99809508	GM12878	blood:	n/a	n/a
2	ATF2	chr7:99808705-99809513	GM12878	blood:	n/a	n/a
3	BATF	chr7:99809022-99809598	GM12878	blood:	n/a	n/a
4	BCL11A	chr7:99808981-99809423	GM12878	blood:	n/a	n/a
5	BCL3	chr7:99809054-99809548	GM12878	blood:	n/a	n/a
6	BCLAF1	chr7:99808822-99809563	GM12878	blood:	n/a	n/a
7	BCLAF1	chr7:99809020-99809584	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:99811418-99811655	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:99809060-99809494	GM12878	blood:	n/a	n/a
10	CEBPB	chr7:99809105-99809377	GM12878	blood:	n/a	n/a
11	CEBPB	chr7:99808759-99810068	GM12878	blood:	n/a	n/a
12	CHD2	chr7:99809018-99809538	GM12878	blood:	n/a	n/a
13	CTCF	chr7:99810195-99810248	GM20000	blood:	n/a	n/a
14	CUX1	chr7:99808984-99809590	GM12878	blood:	n/a	n/a
15	CUX1	chr7:99811417-99811622	GM12878	blood:	n/a	n/a
16	EBF1	chr7:99808965-99809616	GM12878	blood:	n/a	n/a
17	EBF1	chr7:99808949-99809979	GM12878	blood:	n/a	n/a
18	EBF1	chr7:99809021-99809422	GM12878	blood:	n/a	n/a
19	EBF1	chr7:99811131-99811767	GM12878	blood:	n/a	chr7:99811556-99811567 chr7:99811557-99811566 chr7:99811536-99811547
20	EBF1	chr7:99811317-99811735	GM12878	blood:	n/a	chr7:99811556-99811567 chr7:99811557-99811566 chr7:99811536-99811547
21	EBF1	chr7:99811332-99811719	GM12878	blood:	n/a	chr7:99811556-99811567 chr7:99811557-99811566 chr7:99811536-99811547
22	EGR1	chr7:99808578-99808812	K562	blood:	n/a	chr7:99808698-99808712
23	EGR1	chr7:99808606-99808807	GM12878	blood:	n/a	chr7:99808698-99808712
24	EGR1	chr7:99808583-99808807	K562	blood:	n/a	chr7:99808698-99808712
25	EGR1	chr7:99808554-99808844	GM12878	blood:	n/a	chr7:99808698-99808712
26	ELF1	chr7:99808924-99809525	GM12878	blood:	n/a	n/a
27	ELF1	chr7:99808476-99808917	GM12878	blood:	n/a	n/a
28	ELK1	chr7:99808792-99809354	GM12878	blood:	n/a	n/a
29	EP300	chr7:99808901-99809453	GM12878	blood:	n/a	n/a
30	EP300	chr7:99809097-99809414	GM12878	blood:	n/a	n/a
31	ETS1	chr7:99809069-99809472	GM12878	blood:	n/a	n/a
32	FOSL2	chr7:99808668-99809230	HepG2	liver:	n/a	n/a
33	FOSL2	chr7:99810989-99812412	HepG2	liver:	n/a	n/a
34	FOSL2	chr7:99809723-99810045	HepG2	liver:	n/a	n/a
35	FOSL2	chr7:99810287-99810905	HepG2	liver:	n/a	n/a
36	FOXA1	chr7:99810323-99810714	HepG2	liver:	n/a	n/a
37	FOXA2	chr7:99810334-99810523	HepG2	liver:	n/a	n/a
38	FOXM1	chr7:99808766-99809695	GM12878	blood:	n/a	n/a
39	FOXM1	chr7:99808917-99809725	GM12878	blood:	n/a	n/a
40	HNF4A	chr7:99810347-99810532	HepG2	liver:	n/a	n/a
41	IKZF1	chr7:99808851-99809473	GM12878	blood:	n/a	n/a
42	MAX	chr7:99808913-99809316	GM12878	blood:	n/a	n/a
43	MAZ	chr7:99808927-99809561	GM12878	blood:	n/a	n/a
44	MTA3	chr7:99808798-99809565	GM12878	blood:	n/a	n/a
45	MTA3	chr7:99808185-99810079	GM12878	blood:	n/a	n/a
46	MXI1	chr7:99808836-99809438	GM12878	blood:	n/a	n/a
47	NFATC1	chr7:99808807-99809637	GM12878	blood:	n/a	n/a
48	NFIC	chr7:99808898-99809483	GM12878	blood:	n/a	n/a
49	NFIC	chr7:99808143-99809713	GM12878	blood:	n/a	n/a
50	PAX5	chr7:99808962-99809386	GM12878	blood:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99806315..99809110-chr7:99809565..99811179,2	MCF-7	breast:
2	chr7:99795781..99801540-chr7:99806649..99812120,7	K562	blood:
3	chr7:99745511..99748040-chr7:99809267..99811160,3	MCF-7	breast:
4	chr7:99806182..99808834-chr7:99809702..99811286,2	MCF-7	breast:
5	chr7:99724514..99726891-chr7:99806728..99809263,2	K562	blood:
6	chr7:99760958..99763450-chr7:99810400..99812602,2	K562	blood:
7	chr7:99806315..99809110-chr7:99809565..99811179,2	MCF-7	breast:
8	chr7:99806182..99808834-chr7:99809702..99811286,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPC2-2	chr7:99809558-99809617	NONHSAT122350
2	lnc-GPC2-2	chr7:99806591-99809617	NONHSAT122348
3	lnc-GPC2-2	chr7:99810670-99810756	NONHSAT122347
4	lnc-GPC2-2	chr7:99810646-99811247	NONHSAT122348
5	lnc-GPC2-2	chr7:99810576-99810756	NONHSAT122350
6	lnc-GPC2-2	chr7:99806586-99809617	NONHSAT122347

No data

Variant related genes	Relation type
ENSG00000239521	TF binding region
STAG3	TF binding region
PVRIG	TF binding region
ENSG00000242798	chromatin interactions
ENSG00000066923	chromatin interactions
ENSG00000188186	chromatin interactions

Extended variants
information (count: 168 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:168 , 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	rs528441676	chr7:99808049-99808050	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs17249588	chr7:99808097-99808098	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs543198669	chr7:99808110-99808111	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs1637001	chr7:99808151-99808152	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs181378504	chr7:99808179-99808180	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs548032661	chr7:99808247-99808248	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs532544672	chr7:99808263-99808264	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs185996022	chr7:99808315-99808316	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs530338604	chr7:99808403-99808404	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs530289623	chr7:99808413-99808414	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs548818184	chr7:99808469-99808470	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs111572536	chr7:99808502-99808503	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs559684812	chr7:99808514-99808515	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs190816535	chr7:99808522-99808523	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs113558936	chr7:99808587-99808588	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs146963129	chr7:99808591-99808592	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs369421248	chr7:99808592-99808593	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs553568781	chr7:99808618-99808619	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs374273470	chr7:99808631-99808632	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs377541743	chr7:99808651-99808652	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs147584531	chr7:99808689-99808690	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs61749910	chr7:99808703-99808704	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs147288707	chr7:99808704-99808705	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs139887928	chr7:99808709-99808710	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs370756775	chr7:99808732-99808733	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs373006017	chr7:99808749-99808750	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs376074397	chr7:99808759-99808760	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs202156227	chr7:99808765-99808766	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs112524836	chr7:99808780-99808781	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs149417280	chr7:99808790-99808791	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs201135300	chr7:99808794-99808795	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs377387827	chr7:99808874-99808875	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs575995318	chr7:99808894-99808895	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs531965284	chr7:99808962-99808963	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs543426645	chr7:99809007-99809008	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs80044214	chr7:99809032-99809033	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs532260477	chr7:99809033-99809034	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs368651874	chr7:99809044-99809045	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs370467752	chr7:99809067-99809068	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs199936186	chr7:99809071-99809072	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs371789529	chr7:99809073-99809074	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs374856074	chr7:99809080-99809081	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs367599225	chr7:99809091-99809092	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs144728061	chr7:99809113-99809114	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs548870528	chr7:99809120-99809121	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs145943526	chr7:99809162-99809163	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs35274959	chr7:99809259-99809260	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs374391423	chr7:99809260-99809261	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs200493852	chr7:99809261-99809262	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs563989777	chr7:99809269-99809270	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99790000-99808800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:99790000-99817000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:99795600-99812200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:99796000-99808400	Weak transcription	Brain Anterior Caudate	brain
5	chr7:99796400-99808800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:99796400-99813000	Weak transcription	Brain Substantia Nigra	brain
7	chr7:99796800-99816800	Weak transcription	Brain Germinal Matrix	brain
8	chr7:99796800-99817000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr7:99798000-99812000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr7:99798200-99811200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:99798600-99810400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:99799000-99816600	Weak transcription	Fetal Brain Female	brain
13	chr7:99799600-99808800	Weak transcription	Brain Hippocampus Middle	brain
14	chr7:99800200-99812000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr7:99801400-99826000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr7:99802600-99808400	Weak transcription	HSMMtube	muscle
17	chr7:99803000-99808400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr7:99803000-99810600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr7:99803000-99816800	Weak transcription	Brain Angular Gyrus	brain
20	chr7:99803200-99808600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:99803200-99813600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr7:99803800-99808800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:99805200-99818400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:99805600-99812800	Enhancers	Primary T cells fromperipheralblood	blood
25	chr7:99805800-99808800	Enhancers	Primary T cells from cord blood	blood
26	chr7:99806000-99810000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr7:99806000-99810000	Flanking Active TSS	GM12878-XiMat	blood
28	chr7:99806000-99812400	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr7:99806200-99808800	Enhancers	Fetal Thymus	thymus
30	chr7:99806200-99809000	Enhancers	Fetal Stomach	stomach
31	chr7:99806200-99809200	Enhancers	Primary B cells from peripheral blood	blood
32	chr7:99806200-99809800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr7:99806800-99809000	Weak transcription	HepG2	liver
34	chr7:99806800-99819000	Weak transcription	Fetal Lung	lung
35	chr7:99807000-99808400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:99807000-99808600	Enhancers	Thymus	Thymus
37	chr7:99807000-99808800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr7:99807000-99808800	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr7:99807200-99808200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr7:99807200-99808400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr7:99807200-99808400	Weak transcription	Small Intestine	intestine
42	chr7:99807200-99808800	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr7:99807200-99808800	Weak transcription	Liver	Liver
44	chr7:99807200-99808800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr7:99807200-99808800	Weak transcription	Spleen	Spleen
46	chr7:99807200-99809000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr7:99807200-99809000	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr7:99807200-99809000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr7:99807200-99809800	Weak transcription	Fetal Intestine Large	intestine
50	chr7:99807200-99828400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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