Variant report

Variant	esv1792388
Chromosome Location	chr7:99468155-99497338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:367)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:99474151-99474402	K562	blood:	n/a	n/a
2	BATF	chr7:99495363-99495629	GM12878	blood:	n/a	n/a
3	BATF	chr7:99495370-99495615	GM12878	blood:	n/a	n/a
4	CCNT2	chr7:99479141-99479415	K562	blood:	n/a	n/a
5	CEBPB	chr7:99479075-99479187	K562	blood:	n/a	n/a
6	CEBPB	chr7:99483580-99483857	HepG2	liver:	n/a	chr7:99483733-99483744
7	CEBPB	chr7:99483619-99483841	A549	lung:	n/a	chr7:99483733-99483744
8	CEBPB	chr7:99483571-99483872	IMR90	lung:	n/a	chr7:99483733-99483744
9	CEBPB	chr7:99483615-99483813	K562	blood:	n/a	chr7:99483733-99483744
10	CEBPD	chr7:99478964-99479384	K562	blood:	n/a	n/a
11	CEBPD	chr7:99478923-99479407	K562	blood:	n/a	n/a
12	CTCF	chr7:99474334-99474359	GM10266	blood:	n/a	n/a
13	CTCF	chr7:99493680-99493830	A549	lung:	n/a	n/a
14	CTCF	chr7:99474258-99474408	MCF-7	breast:	n/a	n/a
15	CTCF	chr7:99474220-99474370	GM12869	blood:	n/a	n/a
16	CTCF	chr7:99474310-99474442	GM12878	blood:	n/a	n/a
17	CTCF	chr7:99474138-99474405	K562	blood:	n/a	n/a
18	CTCF	chr7:99474131-99474563	K562	blood:	n/a	n/a
19	CTCF	chr7:99474229-99474419	HepG2	liver:	n/a	n/a
20	CTCF	chr7:99474280-99474399	MCF-7	breast:	n/a	n/a
21	CTCF	chr7:99474404-99474411	HepG2	liver:	n/a	n/a
22	CTCF	chr7:99470420-99470570	GM12873	blood:	n/a	n/a
23	CTCF	chr7:99474283-99474412	NHEK	skin:	n/a	n/a
24	CTCF	chr7:99474340-99474490	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:99474319-99474403	HepG2	liver:	n/a	n/a
26	CTCF	chr7:99474380-99474530	A549	lung:	n/a	n/a
27	CTCF	chr7:99474235-99474453	K562	blood:	n/a	n/a
28	CTCF	chr7:99474300-99474450	HL-60	blood:	n/a	n/a
29	CTCF	chr7:99474277-99474439	GM12878	blood:	n/a	n/a
30	CTCF	chr7:99474264-99474324	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:99474200-99474350	K562	blood:	n/a	n/a
32	CTCF	chr7:99474220-99474370	HepG2	liver:	n/a	n/a
33	CTCF	chr7:99474300-99474450	NB4	blood:	n/a	n/a
34	CTCF	chr7:99474180-99474330	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr7:99470540-99470690	BE2_C	brain:	n/a	n/a
36	CTCF	chr7:99484360-99484510	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr7:99474167-99474529	K562	blood:	n/a	n/a
38	CUX1	chr7:99474293-99474425	K562	blood:	n/a	n/a
39	CUX1	chr7:99479017-99479244	K562	blood:	n/a	n/a
40	E2F4	chr7:99481032-99481097	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr7:99490975-99491288	GM12878	blood:	n/a	n/a
42	EBF1	chr7:99495307-99495695	GM12878	blood:	n/a	n/a
43	EBF1	chr7:99495392-99495703	GM12878	blood:	n/a	n/a
44	ELF1	chr7:99474123-99474573	K562	blood:	n/a	chr7:99474343-99474356
45	EP300	chr7:99478972-99479393	K562	blood:	n/a	n/a
46	FOSL2	chr7:99494189-99494969	HepG2	liver:	n/a	n/a
47	GABPA	chr7:99495268-99495788	HL-60	blood:	n/a	n/a
48	GABPA	chr7:99495137-99495884	HL-60	blood:	n/a	n/a
49	GATA1	chr7:99478807-99479579	K562	blood:	n/a	chr7:99479245-99479254
50	GATA2	chr7:99478902-99479415	K562	blood:	n/a	chr7:99479245-99479254

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99475820-99475870	CMK	blood:	n/a
2	chr7:99475820-99475870	CMK	blood:	n/a
3	chr7:99475820-99475870	SK-N-SH_RA	brain:	n/a
4	chr7:99495452-99495502	AG04449	skin:	fetal
5	chr7:99474543-99474593	CMK	blood:	n/a
6	chr7:99486165-99486215	A549	lung:	n/a
7	chr7:99475820-99475870	HRCEpiC	kidney:	n/a
8	chr7:99495452-99495502	Hepatocyte	liver:	n/a
9	chr7:99486165-99486215	BE2_C	brain:	n/a
10	chr7:99495452-99495502	U87	brain:	n/a
11	chr7:99475824-99475874	U87	brain:	n/a
12	chr7:99474543-99474593	LNCaP	prostate:	n/a
13	chr7:99486165-99486215	PANC-1	pancreas:	n/a
14	chr7:99486165-99486215	NHBE	bronchial:	n/a
15	chr7:99475824-99475874	LNCaP	prostate:	n/a
16	chr7:99475820-99475870	NT2-D1	testis:	n/a
17	chr7:99488474-99488524	IMR90	lung:	fetal
18	chr7:99475820-99475870	IMR90	lung:	fetal
19	chr7:99474543-99474593	SK-N-SH_RA	brain:	n/a
20	chr7:99495452-99495502	CMK	blood:	n/a
21	chr7:99488474-99488524	HCT-116	colon:	n/a
22	chr7:99475820-99475870	SK-N-SH	brain:	n/a
23	chr7:99495452-99495502	HRCEpiC	kidney:	n/a
24	chr7:99474543-99474593	HMEC	breast:	n/a
25	chr7:99488474-99488524	SK-N-SH	brain:	n/a
26	chr7:99486165-99486215	GM12892	blood:	n/a
27	chr7:99495452-99495502	GM12891	blood:	n/a
28	chr7:99475824-99475874	IMR90	lung:	fetal
29	chr7:99488474-99488524	GM12891	blood:	n/a
30	chr7:99488474-99488524	PANC-1	pancreas:	n/a
31	chr7:99488474-99488524	GM06990	blood:	n/a
32	chr7:99475824-99475874	HNPCEpiC	eye:	n/a
33	chr7:99475824-99475874	NH-A	brain:	n/a
34	chr7:99474543-99474593	GM06990	blood:	n/a
35	chr7:99475824-99475874	HRE	kidney:	n/a
36	chr7:99474543-99474593	SK-N-MC	brain:	n/a
37	chr7:99475824-99475874	Hela-S3	cervix:	n/a
38	chr7:99495452-99495502	AoSMC	blood vessel:	n/a
39	chr7:99488474-99488524	NB4	blood:	n/a
40	chr7:99474543-99474593	HRPEpiC	eye:	n/a
41	chr7:99475820-99475870	BE2_C	brain:	n/a
42	chr7:99488474-99488524	MCF-7	breast:	n/a
43	chr7:99495452-99495502	SK-N-SH	brain:	n/a
44	chr7:99486165-99486215	ovcar-3	ovarian:	n/a
45	chr7:99475820-99475870	GM12878	blood:	n/a
46	chr7:99475820-99475870	AG10803	skin:	n/a
47	chr7:99474543-99474593	Caco-2	colon:	n/a
48	chr7:99474543-99474593	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:99488474-99488524	HEK293	kidney:	embryo
50	chr7:99486165-99486215	Hepatocyte	liver:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99479801..99482615-chr7:99515257..99518045,2	MCF-7	breast:
2	chr7:99481318..99483626-chr7:99494027..99496823,2	K562	blood:
3	chr7:99497251..99500127-chr7:99514363..99515928,2	K562	blood:
4	chr7:99466355..99469121-chr7:99494728..99496398,2	K562	blood:
5	chr7:99494836..99497202-chr7:99514920..99517849,4	K562	blood:
6	chr7:99493289..99496091-chr7:99505749..99508746,2	K562	blood:
7	chr7:99496614..99498175-chr7:99517020..99518576,2	MCF-7	breast:
8	chr7:99481318..99483626-chr7:99494027..99496823,2	K562	blood:
9	chr7:99488840..99491741-chr7:99492480..99496250,3	K562	blood:
10	chr7:99493888..99497270-chr7:99498893..99502551,4	K562	blood:
11	chr7:99489288..99492873-chr7:99495925..99498517,3	K562	blood:
12	chr7:99485783..99488764-chr7:99489956..99491818,2	K562	blood:
13	chr7:99489288..99492873-chr7:99495925..99498517,3	K562	blood:
14	chr7:99491373..99493924-chr7:99497017..99498799,2	K562	blood:
15	chr7:99491373..99493924-chr7:99497017..99498799,2	K562	blood:
16	chr7:99462714..99465600-chr7:99478263..99479767,2	K562	blood:
17	chr7:99497096..99498693-chr7:99515459..99517111,2	MCF-7	breast:
18	chr7:99363955..99367297-chr7:99492725..99495591,3	K562	blood:
19	chr7:99493415..99495874-chr7:99516388..99518156,3	MCF-7	breast:
20	chr7:99485783..99488764-chr7:99489956..99491818,2	K562	blood:
21	chr7:99494836..99497202-chr7:99514926..99517849,2	K562	blood:
22	chr7:99470145..99472550-chr7:99473069..99474850,2	K562	blood:
23	chr7:99488840..99491741-chr7:99492480..99496250,3	K562	blood:
24	chr1:37196801..37197670-chr7:99474858..99475858,2	K562	blood:
25	chr7:99490457..99493284-chr7:99499457..99501243,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP3A43-5	chr7:99476463-99476904	expReg_chr7_6295_+

No data

Variant related genes	Relation type
OR2AE1	TF binding region
CYP3A52P	TF binding region
OR2AE1	CpG island
CYP3A52P	CpG island
ENSG00000273407	chromatin interactions
ENSG00000244623	chromatin interactions
ENSG00000260445	chromatin interactions
ENSG00000146833	chromatin interactions

Extended variants
information (count: 1236 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547634192	chr7:99468156-99468157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559717277	chr7:99468248-99468249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115509244	chr7:99468256-99468257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548252081	chr7:99468297-99468298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569755730	chr7:99468338-99468339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528716506	chr7:99468356-99468357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537097969	chr7:99468369-99468370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552011644	chr7:99468370-99468371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547279469	chr7:99468389-99468390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112934728	chr7:99468432-99468433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139355707	chr7:99468467-99468468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34360908	chr7:99468556-99468557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547113615	chr7:99468557-99468558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71515288	chr7:99468571-99468572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553609255	chr7:99468581-99468582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574860506	chr7:99468585-99468586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369796692	chr7:99468586-99468587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575570814	chr7:99468594-99468595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556897062	chr7:99468595-99468596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201909464	chr7:99468599-99468600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556726593	chr7:99468632-99468633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575237005	chr7:99468639-99468640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150071408	chr7:99468642-99468643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557986327	chr7:99468684-99468685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576952963	chr7:99468710-99468711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538375089	chr7:99468740-99468741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs180836990	chr7:99468811-99468812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559680258	chr7:99468813-99468814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs643386	chr7:99468828-99468829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs140155940	chr7:99468833-99468834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144001892	chr7:99468850-99468851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566913860	chr7:99468861-99468862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376956160	chr7:99468871-99468872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371591281	chr7:99468880-99468881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530440630	chr7:99468915-99468916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552237504	chr7:99468926-99468927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116110372	chr7:99468978-99468979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528683011	chr7:99468988-99468989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535994110	chr7:99469000-99469001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185295367	chr7:99469019-99469020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190262525	chr7:99469020-99469021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568326608	chr7:99469119-99469120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73401897	chr7:99469205-99469206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs78884002	chr7:99469211-99469212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572668973	chr7:99469266-99469267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540785571	chr7:99469284-99469285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374932130	chr7:99469296-99469297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183421272	chr7:99469299-99469300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78870043	chr7:99469334-99469335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76482135	chr7:99469361-99469362	Weak transcription	n/a	n/a	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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99458200-99489600	Weak transcription	Pancreas	Pancrea
2	chr7:99465200-99475400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:99468400-99487200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:99470000-99489600	Weak transcription	Gastric	stomach
5	chr7:99470200-99470400	Enhancers	Primary T cells from cord blood	blood
6	chr7:99470400-99470600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr7:99470400-99486800	Weak transcription	Primary T cells from cord blood	blood
8	chr7:99470400-99487000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:99470600-99474000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr7:99471400-99487000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:99472000-99473800	Weak transcription	Adipose Nuclei	Adipose
12	chr7:99472400-99472800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:99472400-99487200	Weak transcription	Brain Anterior Caudate	brain
14	chr7:99472400-99487400	Weak transcription	Aorta	Aorta
15	chr7:99472600-99487000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr7:99472600-99487200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr7:99472600-99487600	Weak transcription	Lung	lung
18	chr7:99472600-99488800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr7:99472800-99476200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:99473000-99487200	Weak transcription	Brain Substantia Nigra	brain
21	chr7:99473200-99487200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:99473600-99474600	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr7:99473800-99474600	Strong transcription	Adipose Nuclei	Adipose
24	chr7:99474000-99474600	Bivalent Enhancer	K562	blood
25	chr7:99474000-99475400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr7:99474200-99474600	Enhancers	Esophagus	oesophagus
27	chr7:99474600-99487000	Weak transcription	Adipose Nuclei	Adipose
28	chr7:99474800-99487000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr7:99475400-99477400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr7:99476000-99487000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr7:99476200-99476800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:99478200-99487000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr7:99479000-99479200	Enhancers	Thymus	Thymus
34	chr7:99479200-99488800	Weak transcription	Thymus	Thymus
35	chr7:99479800-99499200	Weak transcription	Small Intestine	intestine
36	chr7:99480400-99487800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr7:99480800-99487200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr7:99482600-99487400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr7:99483000-99487200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr7:99484000-99487000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr7:99484000-99487200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:99484200-99487000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr7:99484400-99484600	Active TSS	Spleen	Spleen
44	chr7:99484600-99484800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:99484600-99487200	Weak transcription	Brain Hippocampus Middle	brain
46	chr7:99484600-99487200	Weak transcription	Spleen	Spleen
47	chr7:99484800-99487000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:99484800-99487000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:99484800-99487000	Weak transcription	Placenta	Placenta
50	chr7:99484800-99487200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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