Variant report

Variant	esv16361
Chromosome Location	chr7:99898203-99934029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:996)
CpG islands
(count:1221)
Chromatin interactive
region (count:18)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:99933514-99933890	K562	blood:	n/a	n/a
2	ATF2	chr7:99933587-99933979	GM12878	blood:	n/a	n/a
3	BACH1	chr7:99933388-99934007	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:99915667-99915855	GM12878	blood:	n/a	n/a
5	BATF	chr7:99922916-99923120	GM12878	blood:	n/a	n/a
6	BATF	chr7:99901300-99901503	GM12878	blood:	n/a	n/a
7	BATF	chr7:99931763-99932072	GM12878	blood:	n/a	n/a
8	BATF	chr7:99921172-99921850	GM12878	blood:	n/a	n/a
9	BATF	chr7:99921263-99921667	GM12878	blood:	n/a	n/a
10	BATF	chr7:99902374-99902726	GM12878	blood:	n/a	n/a
11	BATF	chr7:99922294-99922458	GM12878	blood:	n/a	n/a
12	BATF	chr7:99902780-99903057	GM12878	blood:	n/a	n/a
13	BATF	chr7:99902062-99903018	GM12878	blood:	n/a	n/a
14	BATF	chr7:99931291-99931464	GM12878	blood:	n/a	n/a
15	BATF	chr7:99931789-99932008	GM12878	blood:	n/a	n/a
16	BATF	chr7:99933508-99933915	GM12878	blood:	n/a	n/a
17	BATF	chr7:99901285-99901496	GM12878	blood:	n/a	n/a
18	BATF	chr7:99902075-99902343	GM12878	blood:	n/a	n/a
19	BATF	chr7:99933104-99933496	GM12878	blood:	n/a	n/a
20	BATF	chr7:99900718-99901136	GM12878	blood:	n/a	n/a
21	BATF	chr7:99932699-99932942	GM12878	blood:	n/a	n/a
22	BATF	chr7:99900740-99901050	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:99901627-99901859	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:99931741-99932177	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:99903987-99904347	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:99922824-99923053	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:99933147-99933368	GM12878	blood:	n/a	chr7:99933249-99933262
28	BCL11A	chr7:99915598-99915786	GM12878	blood:	n/a	chr7:99915669-99915678
29	BCL11A	chr7:99922169-99922589	GM12878	blood:	n/a	chr7:99922216-99922225
30	BCL11A	chr7:99931855-99932416	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:99931290-99931519	GM12878	blood:	n/a	chr7:99931369-99931378
32	BCL11A	chr7:99899365-99899765	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:99929074-99929275	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:99922866-99923130	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:99915597-99915943	GM12878	blood:	n/a	chr7:99915669-99915678
36	BCL11A	chr7:99901601-99901842	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:99921061-99921746	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:99900777-99901048	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:99902084-99902502	GM12878	blood:	n/a	chr7:99902302-99902311
40	BCL11A	chr7:99902728-99903004	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:99899420-99899769	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:99902046-99902591	GM12878	blood:	n/a	chr7:99902302-99902311
43	BCL11A	chr7:99900720-99901137	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:99931278-99931549	GM12878	blood:	n/a	chr7:99931369-99931378
45	BCL11A	chr7:99933106-99934023	GM12878	blood:	n/a	chr7:99933249-99933262
46	BCL11A	chr7:99921092-99921910	GM12878	blood:	n/a	n/a
47	BCL3	chr7:99933691-99934093	A549	lung:	n/a	n/a
48	BCL3	chr7:99933337-99933993	A549	lung:	n/a	n/a
49	BCLAF1	chr7:99933315-99933964	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:99918692-99918940	HepG2	liver:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99933968-99934018	SK-N-SH	brain:	n/a
2	chr7:99933968-99934018	SK-N-SH	brain:	n/a
3	chr7:99933670-99933720	HRCEpiC	kidney:	n/a
4	chr7:99933548-99933598	IMR90	lung:	fetal
5	chr7:99904875-99904925	CMK	blood:	n/a
6	chr7:99918120-99918170	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:99933428-99933478	GM06990	blood:	n/a
8	chr7:99933543-99933593	Jurkat	blood:	n/a
9	chr7:99904875-99904925	IMR90	lung:	fetal
10	chr7:99933670-99933720	GM12878	blood:	n/a
11	chr7:99933543-99933593	K562	blood:	n/a
12	chr7:99904850-99904900	Hela-S3	cervix:	n/a
13	chr7:99912131-99912181	Caco-2	colon:	n/a
14	chr7:99933717-99933767	T-47D	breast:	n/a
15	chr7:99933530-99933580	ECC-1	luminal epithelium:	n/a
16	chr7:99905334-99905384	HCM	heart:	n/a
17	chr7:99905331-99905381	ProgFib	skin:	n/a
18	chr7:99929438-99929488	SKMC	muscle:	n/a
19	chr7:99933530-99933580	NT2-D1	testis:	n/a
20	chr7:99912131-99912181	AG09319	gingival:	n/a
21	chr7:99933501-99933551	NT2-D1	testis:	n/a
22	chr7:99934001-99934051	NHDF-neo	bronchial:	n/a
23	chr7:99904850-99904900	HAEpiC	amniotic membrane:	n/a
24	chr7:99904875-99904925	HMEC	breast:	n/a
25	chr7:99904850-99904900	Hepatocyte	liver:	n/a
26	chr7:99934001-99934051	GM12891	blood:	n/a
27	chr7:99905331-99905381	A549	lung:	n/a
28	chr7:99933501-99933551	HIPEpiC	eye:	n/a
29	chr7:99933797-99933847	AG09319	gingival:	n/a
30	chr7:99904850-99904900	AoSMC	blood vessel:	n/a
31	chr7:99905334-99905384	HEEpiC	esophagus:	n/a
32	chr7:99934006-99934056	GM19239	blood:	n/a
33	chr7:99933721-99933771	Hela-S3	cervix:	n/a
34	chr7:99904850-99904900	HCT-116	colon:	n/a
35	chr7:99929438-99929488	MCF10A-Er-Src	breast:	n/a
36	chr7:99932089-99932139	HCT-116	colon:	n/a
37	chr7:99933428-99933478	PANC-1	pancreas:	n/a
38	chr7:99933670-99933720	HCF	heart:	n/a
39	chr7:99933501-99933551	AG10803	skin:	n/a
40	chr7:99932089-99932139	HCF	heart:	n/a
41	chr7:99934006-99934056	HRE	kidney:	n/a
42	chr7:99904850-99904900	GM06990	blood:	n/a
43	chr7:99918120-99918170	GM12891	blood:	n/a
44	chr7:99905334-99905384	HIPEpiC	eye:	n/a
45	chr7:99934006-99934056	GM12892	blood:	n/a
46	chr7:99905331-99905381	BE2_C	brain:	n/a
47	chr7:99933797-99933847	NHDF-neo	bronchial:	n/a
48	chr7:99929438-99929488	ECC-1	luminal epithelium:	n/a
49	chr7:99933721-99933771	U87	brain:	n/a
50	chr7:99932089-99932139	A549	lung:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:36876650..36877236-chr7:99933531..99934342,2	Hela-S3	cervix:
2	chr6:26216777..26217754-chr7:99933218..99933721,2	Hela-S3	cervix:
3	chr7:99932234..99937909-chr7:99939373..99942446,6	K562	blood:
4	chr11:18416119..18416955-chr7:99933156..99933912,2	Hela-S3	cervix:
5	chr1:35658693..35659210-chr7:99933428..99934253,2	Hela-S3	cervix:
6	chr7:99932318..99935048-chr7:100026420..100028378,2	MCF-7	breast:
7	chr6:90539369..90540027-chr7:99932976..99933753,2	Hela-S3	cervix:
8	chr7:99932349..99935076-chr7:100025979..100028387,3	K562	blood:
9	chr7:99932595..99935080-chr7:100025979..100028387,3	K562	blood:
10	chr7:99931911..99935442-chr7:99938364..99941933,5	MCF-7	breast:
11	chr7:99933293..99933992-chr7:130794505..130795164,2	Hela-S3	cervix:
12	chr7:6048837..6049368-chr7:99933514..99934016,2	Hela-S3	cervix:
13	chr7:99933438..99934039-chr7:100026430..100027170,2	NB4	blood:
14	chr7:66767136..66768124-chr7:99933487..99934025,2	HCT-116	colon:
15	chr6:7909845..7910649-chr7:99932993..99933972,2	Hela-S3	cervix:
16	chr7:99765936..99768056-chr7:99933468..99935315,2	MCF-7	breast:
17	chr7:99933746..99935432-chr7:100238068..100240501,2	K562	blood:
18	chr7:99715815..99718290-chr7:99932504..99934640,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GATS-3	chr7:99928086-99928176	NONHSAT122354
2	lnc-GATS-1	chr7:99907941-99908299	expReg_chr7_6426_-
3	lnc-GATS-3	chr7:99927647-99927907	NONHSAT122354
4	lnc-PILRB-1	chr7:99933737-99933960	NONHSAT122358
5	lnc-GATS-2	chr7:99913916-99914300	expReg_chr7_6439_-

No data

Variant related genes	Relation type
PMS2P1	TF binding region
ENSG00000201913	TF binding region
STAG3L5P	TF binding region
PILRB	TF binding region
SPDYE3	TF binding region
STAG3L5P-PVRIG2P-PILRB	TF binding region
PMS2P1	CpG island
ENSG00000201913	CpG island
STAG3L5P	CpG island
PILRB	CpG island
SPDYE3	CpG island
STAG3L5P-PVRIG2P-PILRB	CpG island
ENSG00000106305	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000106610	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000128585	chromatin interactions
ENSG00000116560	chromatin interactions
ENSG00000239264	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000078319	chromatin interactions
ENSG00000231721	chromatin interactions
ENSG00000067601	chromatin interactions
ENSG00000106327	chromatin interactions
ENSG00000197093	chromatin interactions
ENSG00000106290	chromatin interactions
ENSG00000118412	chromatin interactions

Extended variants
information (count: 1077 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201432792	chr7:99898208-99898209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570526005	chr7:99898212-99898213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534934445	chr7:99898224-99898225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552976496	chr7:99898300-99898301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574401477	chr7:99898318-99898319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541841935	chr7:99898390-99898391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554559881	chr7:99898626-99898627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557132693	chr7:99898627-99898628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374021025	chr7:99898634-99898635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575418987	chr7:99898654-99898655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573117669	chr7:99898666-99898667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375116977	chr7:99898673-99898674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564721050	chr7:99898682-99898683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112118997	chr7:99898760-99898761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528641095	chr7:99898792-99898793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540951768	chr7:99898888-99898889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369670057	chr7:99899012-99899013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372802515	chr7:99899019-99899020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111592913	chr7:99899039-99899040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111517552	chr7:99899079-99899080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113849516	chr7:99899102-99899103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190599112	chr7:99899104-99899105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182235255	chr7:99899136-99899137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550573216	chr7:99899191-99899192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375985433	chr7:99899250-99899251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562496958	chr7:99899289-99899290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533274304	chr7:99899292-99899293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551549578	chr7:99899334-99899335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370314079	chr7:99899342-99899343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570661128	chr7:99899365-99899366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs67951715	chr7:99899445-99899446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541009939	chr7:99899454-99899455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546920125	chr7:99899531-99899532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536593483	chr7:99899788-99899789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535595176	chr7:99899790-99899791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58081351	chr7:99899836-99899837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568351949	chr7:99900150-99900151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535705924	chr7:99900167-99900168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113254600	chr7:99900225-99900226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556997584	chr7:99900260-99900261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537916475	chr7:99900320-99900321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575281635	chr7:99900442-99900443	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs377069422	chr7:99900468-99900469	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs559285860	chr7:99900471-99900472	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557549304	chr7:99900487-99900488	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573434242	chr7:99900497-99900498	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs371038670	chr7:99900590-99900591	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs540461909	chr7:99900669-99900670	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs562271028	chr7:99900670-99900671	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs202223330	chr7:99900704-99900705	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:635 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99870200-99916800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:99870200-99932800	Weak transcription	Ovary	ovary
3	chr7:99870400-99901600	Weak transcription	Thymus	Thymus
4	chr7:99870400-99904600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr7:99870400-99917000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:99870400-99917000	Weak transcription	Fetal Muscle Leg	muscle
7	chr7:99870400-99917600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:99870400-99923400	Weak transcription	Fetal Intestine Large	intestine
9	chr7:99870400-99932600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:99870600-99898800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr7:99870600-99904600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:99870600-99916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:99870600-99923400	Weak transcription	Spleen	Spleen
14	chr7:99870600-99926200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr7:99870600-99932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:99870800-99904600	Weak transcription	Dnd41	blood
17	chr7:99871000-99917000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr7:99871000-99923000	Weak transcription	Brain Germinal Matrix	brain
19	chr7:99874400-99932800	Weak transcription	Brain Angular Gyrus	brain
20	chr7:99880400-99917800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:99882000-99903000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:99884400-99916000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:99886800-99901600	Weak transcription	Fetal Stomach	stomach
24	chr7:99887400-99932800	Weak transcription	Brain Anterior Caudate	brain
25	chr7:99889400-99915000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:99890200-99914200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr7:99890400-99901000	Weak transcription	Fetal Thymus	thymus
28	chr7:99890400-99917000	Weak transcription	Fetal Brain Female	brain
29	chr7:99892800-99901800	Weak transcription	Fetal Intestine Small	intestine
30	chr7:99893600-99914200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:99893600-99917000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr7:99893600-99917800	Weak transcription	Lung	lung
33	chr7:99893600-99918000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:99896400-99917000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr7:99896600-99924600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:99896600-99931800	Weak transcription	K562	blood
37	chr7:99897600-99933200	Weak transcription	Pancreas	Pancrea
38	chr7:99898000-99932800	Weak transcription	Brain Substantia Nigra	brain
39	chr7:99899200-99901600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr7:99900200-99902400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr7:99901000-99902400	Enhancers	Primary B cells from peripheral blood	blood
42	chr7:99901000-99902400	Enhancers	Fetal Thymus	thymus
43	chr7:99901200-99902400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr7:99901200-99923400	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr7:99901600-99901800	Enhancers	Thymus	Thymus
46	chr7:99901600-99902000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:99901600-99902600	Strong transcription	Fetal Stomach	stomach
48	chr7:99901800-99902200	Weak transcription	Thymus	Thymus
49	chr7:99901800-99903200	Strong transcription	Fetal Intestine Small	intestine
50	chr7:99902000-99916800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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