Variant report

Variant	nsv889239
Chromosome Location	chr7:136923730-136994013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:206)
CpG islands
(count:429)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:206 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:136992921-136992933	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr7:136947739-136947900	IMR90	lung:	n/a	n/a
3	CEBPB	chr7:136945439-136945666	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr7:136956417-136956716	HepG2	liver:	n/a	chr7:136956559-136956570
5	CEBPB	chr7:136928509-136928742	HepG2	liver:	n/a	n/a
6	CTCF	chr7:136989340-136989490	HAc	cerebellar:	n/a	n/a
7	CTCF	chr7:136953266-136953316	GM20000	blood:	n/a	n/a
8	CTCF	chr7:136972460-136972610	HCT-116	colon:	n/a	n/a
9	CTCF	chr7:136989400-136989550	HCM	heart:	n/a	n/a
10	CTCF	chr7:136972460-136972610	GM12878	blood:	n/a	n/a
11	CTCF	chr7:136972460-136972610	AG04450	lung:	n/a	n/a
12	CTCF	chr7:136972460-136972610	GM12864	blood:	n/a	n/a
13	CTCF	chr7:136945500-136945650	NHDF-neo	bronchial:	n/a	n/a
14	CTCF	chr7:136972520-136972670	RPTEC	kidney:	n/a	n/a
15	CTCF	chr7:136972442-136972780	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr7:136972480-136972630	BJ	skin:	n/a	n/a
17	CTCF	chr7:136989460-136989610	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr7:136989480-136989630	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr7:136949778-136949828	GM13976	blood:	n/a	n/a
20	CTCF	chr7:136972540-136972651	LNCaP	prostate:	n/a	n/a
21	CTCF	chr7:136972580-136972730	HVMF	connective:	n/a	n/a
22	CTCF	chr7:136972520-136972670	AG09319	gingival:	n/a	n/a
23	CTCF	chr7:136972520-136972670	WI-38	lung:	n/a	n/a
24	CTCF	chr7:136972529-136972658	LNCaP	prostate:	n/a	n/a
25	CTCF	chr7:136972522-136972625	GM12878	blood:	n/a	n/a
26	CTCF	chr7:136972500-136972650	HMF	breast:	n/a	n/a
27	CTCF	chr7:136972520-136972670	BJ	skin:	n/a	n/a
28	CTCF	chr7:136972568-136972617	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr7:136972559-136972625	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr7:136972480-136972630	K562	blood:	n/a	n/a
31	CTCF	chr7:136955760-136955910	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr7:136972540-136972690	AG09319	gingival:	n/a	n/a
33	CTCF	chr7:136989560-136989613	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:136972480-136972630	RPTEC	kidney:	n/a	n/a
35	CTCF	chr7:136984100-136984250	GM06990	blood:	n/a	n/a
36	CTCF	chr7:136972500-136972650	NHEK	skin:	n/a	n/a
37	CTCF	chr7:136989420-136989570	HCM	heart:	n/a	n/a
38	CTCF	chr7:136972450-136972726	K562	blood:	n/a	n/a
39	CTCF	chr7:136989540-136989690	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:136972521-136972613	HepG2	liver:	n/a	n/a
41	CTCF	chr7:136989480-136989630	HVMF	connective:	n/a	n/a
42	CTCF	chr7:136989560-136989710	HCFaa	heart:	n/a	n/a
43	CTCF	chr7:136926580-136926730	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr7:136972460-136972610	HCM	heart:	n/a	n/a
45	CTCF	chr7:136972540-136972690	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr7:136972460-136972610	GM12865	blood:	n/a	n/a
47	CTCF	chr7:136989420-136989570	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr7:136972560-136972710	HPF	lung:	n/a	n/a
49	CTCF	chr7:136972430-136972770	GM12878	blood:	n/a	n/a
50	CTCF	chr7:136989561-136989603	Gliobla	brain:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:136960138-136960188	BE2_C	brain:	n/a
2	chr7:136944526-136944576	GM12891	blood:	n/a
3	chr7:136960138-136960188	BE2_C	brain:	n/a
4	chr7:136944526-136944576	GM12891	blood:	n/a
5	chr7:136944526-136944576	ProgFib	skin:	n/a
6	chr7:136953057-136953107	BE2_C	brain:	n/a
7	chr7:136973838-136973888	CMK	blood:	n/a
8	chr7:136989898-136989948	HCM	heart:	n/a
9	chr7:136953057-136953107	GM12878	blood:	n/a
10	chr7:136927099-136927149	AG09309	skin:	n/a
11	chr7:136927099-136927149	GM12878	blood:	n/a
12	chr7:136928644-136928694	HRE	kidney:	n/a
13	chr7:136989898-136989948	HL-60	blood:	n/a
14	chr7:136953057-136953107	HCF	heart:	n/a
15	chr7:136927099-136927149	ECC-1	luminal epithelium:	n/a
16	chr7:136928644-136928694	PrEC	prostate:	n/a
17	chr7:136944526-136944576	HMEC	breast:	n/a
18	chr7:136928644-136928694	NB4	blood:	n/a
19	chr7:136960138-136960188	NH-A	brain:	n/a
20	chr7:136944526-136944576	AG09319	gingival:	n/a
21	chr7:136960138-136960188	GM12891	blood:	n/a
22	chr7:136960138-136960188	HEK293	kidney:	embryo
23	chr7:136928644-136928694	GM06990	blood:	n/a
24	chr7:136944526-136944576	SK-N-SH_RA	brain:	n/a
25	chr7:136927099-136927149	A549	lung:	n/a
26	chr7:136944526-136944576	HCM	heart:	n/a
27	chr7:136953057-136953107	SK-N-SH_RA	brain:	n/a
28	chr7:136973838-136973888	PrEC	prostate:	n/a
29	chr7:136944526-136944576	T-47D	breast:	n/a
30	chr7:136989898-136989948	NHBE	bronchial:	n/a
31	chr7:136973838-136973888	NH-A	brain:	n/a
32	chr7:136960138-136960188	SK-N-MC	brain:	n/a
33	chr7:136927099-136927149	HCM	heart:	n/a
34	chr7:136973838-136973888	PANC-1	pancreas:	n/a
35	chr7:136960138-136960188	HCF	heart:	n/a
36	chr7:136989898-136989948	HCF	heart:	n/a
37	chr7:136989898-136989948	HCT-116	colon:	n/a
38	chr7:136960138-136960188	GM12878	blood:	n/a
39	chr7:136928644-136928694	HIPEpiC	eye:	n/a
40	chr7:136973838-136973888	AG10803	skin:	n/a
41	chr7:136973838-136973888	HRCEpiC	kidney:	n/a
42	chr7:136927099-136927149	SK-N-SH_RA	brain:	n/a
43	chr7:136944526-136944576	AG04449	skin:	fetal
44	chr7:136960138-136960188	HRPEpiC	eye:	n/a
45	chr7:136953057-136953107	Caco-2	colon:	n/a
46	chr7:136953057-136953107	RPTEC	kidney:	n/a
47	chr7:136989898-136989948	ProgFib	skin:	n/a
48	chr7:136973838-136973888	BE2_C	brain:	n/a
49	chr7:136927099-136927149	AG10803	skin:	n/a
50	chr7:136927099-136927149	LNCaP	prostate:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:136926388..136928401-chr7:136930158..136932908,2	K562	blood:
2	chr7:136939425..136941087-chr7:136941192..136943070,2	K562	blood:
3	chr7:136960021..136961767-chr7:136965044..136967236,2	K562	blood:
4	chr7:136939425..136941087-chr7:136941192..136943070,2	K562	blood:
5	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:
6	chr7:136926388..136929879-chr7:136930158..136932908,3	K562	blood:
7	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
8	chr7:136915442..136917934-chr7:136955995..136958425,2	K562	blood:
9	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
10	chr7:136926388..136928401-chr7:136930158..136932908,2	K562	blood:
11	chr7:136930142..136933282-chr7:136935160..136937647,3	K562	blood:
12	chr7:136926388..136929879-chr7:136930158..136932908,3	K562	blood:
13	chr7:136915740..136917893-chr7:136923118..136925670,2	K562	blood:
14	chr7:136930142..136933282-chr7:136935160..136937647,3	K562	blood:
15	chr7:136960021..136961767-chr7:136965044..136967236,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000202023	TF binding region
ENSG00000202023	CpG island

Extended variants
information (count: 2621 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2621 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs891586	chr7:136923730-136923731	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571820554	chr7:136923751-136923752	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546519970	chr7:136923808-136923809	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566656512	chr7:136923844-136923845	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188086177	chr7:136923903-136923904	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548676935	chr7:136923947-136923948	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568483496	chr7:136923959-136923960	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537013209	chr7:136923996-136923997	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557639724	chr7:136924005-136924006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192903661	chr7:136924043-136924044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139773200	chr7:136924063-136924064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553182507	chr7:136924077-136924078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573076706	chr7:136924121-136924122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374385743	chr7:136924122-136924123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527772672	chr7:136924144-136924145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60204827	chr7:136924159-136924160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184504803	chr7:136924174-136924175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144487135	chr7:136924226-136924227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575203906	chr7:136924237-136924238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372437178	chr7:136924253-136924254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543812432	chr7:136924271-136924272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370775726	chr7:136924296-136924297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577894888	chr7:136924297-136924298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189285863	chr7:136924300-136924301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560411097	chr7:136924306-136924307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189285640	chr7:136924320-136924321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544998299	chr7:136924339-136924340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550800311	chr7:136924361-136924362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548713141	chr7:136924416-136924417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562119795	chr7:136924417-136924418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377540124	chr7:136924429-136924430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531029607	chr7:136924434-136924435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550736535	chr7:136924473-136924474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369840734	chr7:136924476-136924477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570807665	chr7:136924490-136924491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77653916	chr7:136924541-136924542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373737060	chr7:136924542-136924543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146137727	chr7:136924545-136924546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140106420	chr7:136924547-136924548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560252168	chr7:136924552-136924553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555046678	chr7:136924560-136924561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182123741	chr7:136924578-136924579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537931747	chr7:136924579-136924580	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76634878	chr7:136924634-136924635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577539121	chr7:136924635-136924636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184784257	chr7:136924699-136924700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142357393	chr7:136924706-136924707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573886671	chr7:136924733-136924734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542892422	chr7:136924788-136924789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189414684	chr7:136924799-136924800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:609 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136902000-136933800	Weak transcription	Fetal Brain Female	brain
2	chr7:136906600-136925200	Weak transcription	Fetal Stomach	stomach
3	chr7:136909600-136935800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:136909800-136926200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:136909800-136943000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:136911000-136927000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:136911200-136925800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:136911600-136936400	Weak transcription	Fetal Heart	heart
9	chr7:136913400-136937200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr7:136915200-136935000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr7:136917200-136923800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:136920200-136939000	Weak transcription	Fetal Kidney	kidney
13	chr7:136921200-136924600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:136922400-136935600	Weak transcription	Placenta	Placenta
15	chr7:136922600-136924000	Enhancers	Brain Hippocampus Middle	brain
16	chr7:136922800-136923800	Enhancers	Brain Cingulate Gyrus	brain
17	chr7:136923000-136926600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr7:136923000-136928000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr7:136923200-136924000	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:136923200-136925400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:136923200-136926600	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr7:136923200-136939600	Weak transcription	Brain Angular Gyrus	brain
23	chr7:136923200-136940200	Weak transcription	Brain Substantia Nigra	brain
24	chr7:136923600-136924000	Enhancers	Brain Anterior Caudate	brain
25	chr7:136923600-136937800	Weak transcription	Brain Germinal Matrix	brain
26	chr7:136923800-136924000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:136923800-136937600	Weak transcription	Brain Cingulate Gyrus	brain
28	chr7:136924000-136927000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr7:136924000-136933800	Weak transcription	Brain Anterior Caudate	brain
30	chr7:136924000-136936800	Weak transcription	Brain Hippocampus Middle	brain
31	chr7:136924000-136939800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:136924000-136939800	Weak transcription	Fetal Intestine Small	intestine
33	chr7:136924400-136939200	Weak transcription	Aorta	Aorta
34	chr7:136924600-136941400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:136925200-136926000	Strong transcription	Fetal Stomach	stomach
36	chr7:136925400-136928800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:136925800-136927400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:136926000-136926600	Weak transcription	Fetal Stomach	stomach
39	chr7:136926200-136926800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr7:136926200-136927200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:136926400-136927400	Enhancers	Fetal Lung	lung
42	chr7:136926600-136927200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:136926600-136927200	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr7:136926600-136927200	Genic enhancers	Fetal Stomach	stomach
45	chr7:136926600-136927400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:136926600-136928600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
47	chr7:136926600-136943400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr7:136926800-136929800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr7:136927000-136927400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr7:136927000-136927600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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