Variant report

Variant	nsv888761
Chromosome Location	chr7:97829492-97844578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:450)
CpG islands
(count:2077)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97841106-97841413	HepG2	liver:	n/a	n/a
2	ATF2	chr7:97832563-97833050	GM12878	blood:	n/a	n/a
3	ATF2	chr7:97831639-97832231	GM12878	blood:	n/a	n/a
4	ATF2	chr7:97832597-97832988	GM12878	blood:	n/a	n/a
5	ATF2	chr7:97831540-97832306	GM12878	blood:	n/a	n/a
6	ATF2	chr7:97829493-97830274	GM12878	blood:	n/a	n/a
7	ATF3	chr7:97841200-97841340	K562	blood:	n/a	n/a
8	BACH1	chr7:97840715-97840870	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:97839948-97840290	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:97831662-97832223	GM12878	blood:	n/a	n/a
11	BATF	chr7:97829716-97830130	GM12878	blood:	n/a	n/a
12	BATF	chr7:97832660-97833056	GM12878	blood:	n/a	n/a
13	BATF	chr7:97831736-97832057	GM12878	blood:	n/a	n/a
14	BATF	chr7:97829731-97830105	GM12878	blood:	n/a	n/a
15	BATF	chr7:97832640-97833033	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:97829655-97830038	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:97832623-97833012	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:97831709-97832174	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:97831638-97832199	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:97832657-97832962	GM12878	blood:	n/a	n/a
21	BCL3	chr7:97831739-97832179	GM12878	blood:	n/a	n/a
22	BCL3	chr7:97831708-97832225	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:97831606-97832314	GM12878	blood:	n/a	n/a
24	BCLAF1	chr7:97831633-97832386	GM12878	blood:	n/a	n/a
25	BCLAF1	chr7:97829465-97830220	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:97831481-97833086	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:97840739-97841503	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:97841083-97841121	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:97843618-97843621	K562	blood:	n/a	n/a
30	BHLHE40	chr7:97840950-97841274	K562	blood:	n/a	n/a
31	BHLHE40	chr7:97829559-97830188	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:97841048-97841415	HepG2	liver:	n/a	n/a
33	CCNT2	chr7:97840716-97841121	K562	blood:	n/a	n/a
34	CCNT2	chr7:97841471-97841671	K562	blood:	n/a	n/a
35	CCNT2	chr7:97835012-97835236	K562	blood:	n/a	n/a
36	CEBPB	chr7:97829704-97830041	GM12878	blood:	n/a	n/a
37	CEBPB	chr7:97832592-97833125	GM12878	blood:	n/a	chr7:97833057-97833070
38	CEBPB	chr7:97831597-97832302	GM12878	blood:	n/a	n/a
39	CEBPB	chr7:97841211-97841387	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:97831766-97832109	GM12878	blood:	n/a	n/a
41	CHD1	chr7:97831587-97832480	GM12878	blood:	n/a	n/a
42	CHD2	chr7:97831705-97833052	GM12878	blood:	n/a	n/a
43	CHD2	chr7:97839942-97840021	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr7:97840957-97841477	HepG2	liver:	n/a	n/a
45	CHD2	chr7:97844264-97844285	HepG2	liver:	n/a	n/a
46	CREB1	chr7:97831665-97832292	GM12878	blood:	n/a	n/a
47	CTCF	chr7:97831891-97832103	GM12878	blood:	n/a	n/a
48	CTCF	chr7:97840565-97840717	HepG2	liver:	n/a	chr7:97840589-97840599
49	CTCF	chr7:97841217-97841244	GM12891	blood:	n/a	n/a
50	CTCF	chr7:97832785-97832812	GM12891	blood:	n/a	n/a

(count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97832830-97832880	HEEpiC	esophagus:	n/a
2	chr7:97839870-97839920	NHBE	bronchial:	n/a
3	chr7:97834674-97834724	HMEC	breast:	n/a
4	chr7:97832830-97832880	HEEpiC	esophagus:	n/a
5	chr7:97839870-97839920	NHBE	bronchial:	n/a
6	chr7:97834674-97834724	HMEC	breast:	n/a
7	chr7:97841071-97841121	NB4	blood:	n/a
8	chr7:97841941-97841991	AG10803	skin:	n/a
9	chr7:97839870-97839920	HepG2	liver:	n/a
10	chr7:97841440-97841490	NHBE	bronchial:	n/a
11	chr7:97834891-97834941	HCPEpiC	choroid plexus:	n/a
12	chr7:97841334-97841384	PrEC	prostate:	n/a
13	chr7:97832841-97832891	U87	brain:	n/a
14	chr7:97840014-97840064	HCM	heart:	n/a
15	chr7:97841440-97841490	LNCaP	prostate:	n/a
16	chr7:97842268-97842318	GM19239	blood:	n/a
17	chr7:97841941-97841991	GM19239	blood:	n/a
18	chr7:97841941-97841991	AoSMC	blood vessel:	n/a
19	chr7:97841447-97841497	RPTEC	kidney:	n/a
20	chr7:97835841-97835891	BE2_C	brain:	n/a
21	chr7:97836563-97836613	AG04449	skin:	fetal
22	chr7:97835841-97835891	SAEC	small airway:	n/a
23	chr7:97842268-97842318	K562	blood:	n/a
24	chr7:97835192-97835242	H1-hESC	embryonic stem cell:	embryo
25	chr7:97835192-97835242	HNPCEpiC	eye:	n/a
26	chr7:97841941-97841991	GM12878	blood:	n/a
27	chr7:97844391-97844441	NHBE	bronchial:	n/a
28	chr7:97838663-97838713	AG10803	skin:	n/a
29	chr7:97836563-97836613	K562	blood:	n/a
30	chr7:97834674-97834724	SK-N-SH_RA	brain:	n/a
31	chr7:97832841-97832891	HRPEpiC	eye:	n/a
32	chr7:97833154-97833204	Hela-S3	cervix:	n/a
33	chr7:97844391-97844441	GM12878	blood:	n/a
34	chr7:97841513-97841563	SK-N-SH	brain:	n/a
35	chr7:97844391-97844441	PrEC	prostate:	n/a
36	chr7:97841071-97841121	GM06990	blood:	n/a
37	chr7:97834674-97834724	AG04449	skin:	fetal
38	chr7:97838735-97838785	HUVEC	blood vessel:	n/a
39	chr7:97831974-97832024	GM19239	blood:	n/a
40	chr7:97831974-97832024	GM12892	blood:	n/a
41	chr7:97835841-97835891	AG04449	skin:	fetal
42	chr7:97842268-97842318	MCF-7	breast:	n/a
43	chr7:97841001-97841051	AoSMC	blood vessel:	n/a
44	chr7:97838735-97838785	HCPEpiC	choroid plexus:	n/a
45	chr7:97834623-97834673	GM12891	blood:	n/a
46	chr7:97838735-97838785	AG09309	skin:	n/a
47	chr7:97834674-97834724	Hela-S3	cervix:	n/a
48	chr7:97841001-97841051	PrEC	prostate:	n/a
49	chr7:97834623-97834673	HCPEpiC	choroid plexus:	n/a
50	chr7:97838659-97838709	HIPEpiC	eye:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97843013..97845825-chr7:97853837..97855430,2	MCF-7	breast:
2	chr7:97843965..97846398-chr7:97856911..97858412,2	K562	blood:
3	chr7:97842812..97845120-chr7:97865672..97868033,2	K562	blood:
4	chr7:97815298..97817791-chr7:97831369..97832934,2	MCF-7	breast:
5	chr7:97831874..97833996-chr7:97840662..97842294,3	K562	blood:
6	chr7:97829526..97831904-chr7:97833458..97836322,3	K562	blood:
7	chr7:97840173..97842487-chr7:97845725..97848039,2	MCF-7	breast:
8	chr7:97839794..97841701-chr7:97843448..97845628,2	MCF-7	breast:
9	chr10:8099641..8101523-chr7:97840811..97843007,2	MCF-7	breast:
10	chr7:97829526..97831904-chr7:97833458..97836322,3	K562	blood:
11	chr7:97834447..97836459-chr7:97921103..97922884,2	K562	blood:
12	chr7:97839660..97842920-chr7:97872632..97874833,3	K562	blood:
13	chr7:97844457..97846470-chr7:97865336..97867376,2	MCF-7	breast:
14	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
15	chr7:97840856..97842377-chr7:97845637..97848224,2	MCF-7	breast:
16	chr7:97826253..97828518-chr7:97833038..97835255,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BHLHA15-1	chr7:97842411-97844754	NONHSAT122177
2	lnc-BHLHA15-1	chr7:97840778-97840810	NONHSAT122177
3	lnc-BHLHA15-1	chr7:97841568-97841603	NONHSAT122177

No data

Variant related genes	Relation type
BHLHA15	TF binding region
BHLHA15	CpG island
ENSG00000180535	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000107485	chromatin interactions

Extended variants
information (count: 645 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11975025	chr7:97829492-97829493	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116896023	chr7:97829516-97829517	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs148848025	chr7:97829553-97829554	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs113656600	chr7:97829577-97829578	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs529167708	chr7:97829589-97829590	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs11534031	chr7:97829605-97829606	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570659037	chr7:97829612-97829613	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569186972	chr7:97829645-97829646	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537620244	chr7:97829659-97829660	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73710392	chr7:97829737-97829738	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs117683966	chr7:97829805-97829806	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs566959157	chr7:97829819-97829820	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs143575218	chr7:97829879-97829880	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs192907354	chr7:97829913-97829914	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs567942842	chr7:97829986-97829987	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs183844775	chr7:97830019-97830020	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533147642	chr7:97830036-97830037	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556911675	chr7:97830041-97830042	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575168983	chr7:97830060-97830061	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188736507	chr7:97830068-97830069	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193284496	chr7:97830123-97830124	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138102097	chr7:97830128-97830129	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369184941	chr7:97830129-97830130	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184215619	chr7:97830217-97830218	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572627982	chr7:97830227-97830228	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146479843	chr7:97830248-97830249	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201081690	chr7:97830283-97830284	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561582789	chr7:97830315-97830316	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115216722	chr7:97830332-97830333	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544227620	chr7:97830340-97830341	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4729412	chr7:97830352-97830353	Weak transcription Strong transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188230767	chr7:97830446-97830447	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572061576	chr7:97830478-97830479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77423436	chr7:97830481-97830482	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551774468	chr7:97830531-97830532	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564750327	chr7:97830562-97830563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs13228463	chr7:97830588-97830589	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs28457167	chr7:97830704-97830705	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191532483	chr7:97830725-97830726	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141148911	chr7:97830738-97830739	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538518831	chr7:97830749-97830750	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562271112	chr7:97830796-97830797	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144849267	chr7:97830818-97830819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571915112	chr7:97830821-97830822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138825821	chr7:97830860-97830861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557752094	chr7:97830865-97830866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572588988	chr7:97830871-97830872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539969106	chr7:97830889-97830890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555141124	chr7:97830904-97830905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56186084	chr7:97830911-97830912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	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
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97765800-97840800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:97782400-97839800	Weak transcription	Fetal Brain Male	brain
3	chr7:97793400-97841000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr7:97808400-97833600	Weak transcription	Stomach Mucosa	stomach
5	chr7:97808600-97839800	Weak transcription	Right Atrium	heart
6	chr7:97812000-97841000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:97816000-97839200	Weak transcription	Psoas Muscle	Psoas
8	chr7:97816600-97839800	Weak transcription	NH-A	brain
9	chr7:97819200-97834800	Weak transcription	HUVEC	blood vessel
10	chr7:97820600-97830000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:97822200-97829600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr7:97822400-97841000	Weak transcription	K562	blood
13	chr7:97822600-97831200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:97822800-97829600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr7:97822800-97837600	Weak transcription	Fetal Kidney	kidney
16	chr7:97823000-97851000	Weak transcription	HSMMtube	muscle
17	chr7:97823600-97833400	Weak transcription	A549	lung
18	chr7:97823800-97832600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:97823800-97834400	Weak transcription	Brain Substantia Nigra	brain
20	chr7:97823800-97840000	Weak transcription	Small Intestine	intestine
21	chr7:97824000-97832600	Weak transcription	Right Ventricle	heart
22	chr7:97824000-97835600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:97824200-97831000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr7:97824200-97831200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr7:97824200-97832200	Weak transcription	Brain Hippocampus Middle	brain
26	chr7:97824200-97833200	Weak transcription	Colon Smooth Muscle	Colon
27	chr7:97824200-97833800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr7:97824200-97834200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:97824400-97834000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:97824400-97834000	Weak transcription	NHLF	lung
31	chr7:97824400-97834600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:97824400-97839800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:97824600-97831400	Weak transcription	NHEK	skin
34	chr7:97824600-97834000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr7:97824600-97839800	Weak transcription	Osteobl	bone
36	chr7:97824600-97840800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr7:97824800-97834600	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr7:97824800-97834800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:97824800-97835000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:97824800-97839800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr7:97824800-97839800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr7:97824800-97840000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:97825000-97831600	Weak transcription	HMEC	breast
44	chr7:97825000-97833400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr7:97825000-97833600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr7:97825000-97834200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr7:97825000-97835000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr7:97825000-97836000	Weak transcription	Brain Angular Gyrus	brain
49	chr7:97825200-97829600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr7:97825200-97829800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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