Variant report

Variant	esv1813148
Chromosome Location	chr7:147796154-147837213
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:147832267-147832555	A549	lung:	n/a	chr7:147832407-147832420 chr7:147832408-147832419 chr7:147832490-147832502 chr7:147832407-147832418 chr7:147832397-147832410
2	CEBPB	chr7:147816621-147816869	K562	blood:	n/a	chr7:147816788-147816799 chr7:147816786-147816799
3	CEBPB	chr7:147805786-147806016	A549	lung:	n/a	chr7:147805894-147805905
4	CEBPB	chr7:147832248-147832531	IMR90	lung:	n/a	chr7:147832407-147832420 chr7:147832408-147832419 chr7:147832490-147832502 chr7:147832407-147832418 chr7:147832397-147832410
5	CEBPB	chr7:147824627-147824827	HepG2	liver:	n/a	chr7:147824680-147824691 chr7:147824717-147824734 chr7:147824679-147824692 chr7:147824678-147824695
6	CEBPB	chr7:147832244-147832684	MCF-7	breast:	n/a	chr7:147832407-147832420 chr7:147832408-147832419 chr7:147832490-147832502 chr7:147832407-147832418 chr7:147832397-147832410
7	CEBPB	chr7:147832243-147832482	Hela-S3	cervix:	n/a	chr7:147832407-147832420 chr7:147832408-147832419 chr7:147832407-147832418 chr7:147832397-147832410
8	CEBPB	chr7:147805828-147806028	HepG2	liver:	n/a	chr7:147805894-147805905
9	CEBPB	chr7:147805777-147805943	IMR90	lung:	n/a	chr7:147805894-147805905
10	CEBPB	chr7:147832277-147832512	H1-hESC	embryonic stem cell:	n/a	chr7:147832407-147832420 chr7:147832408-147832419 chr7:147832490-147832502 chr7:147832407-147832418 chr7:147832397-147832410
11	CEBPB	chr7:147832255-147832588	HepG2	liver:	n/a	chr7:147832407-147832420 chr7:147832408-147832419 chr7:147832490-147832502 chr7:147832407-147832418 chr7:147832397-147832410
12	CTBP2	chr7:147804868-147805603	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr7:147807340-147807490	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr7:147807300-147807450	K562	blood:	n/a	n/a
15	CTCF	chr7:147807304-147807507	K562	blood:	n/a	n/a
16	CTCF	chr7:147819580-147819730	GM12864	blood:	n/a	chr7:147819684-147819697
17	CTCF	chr7:147807260-147807543	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:147807421-147807430	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr7:147807275-147807510	HepG2	liver:	n/a	n/a
20	CTCF	chr7:147807720-147807870	RPTEC	kidney:	n/a	n/a
21	CTCF	chr7:147807320-147807470	MCF-7	breast:	n/a	n/a
22	CTCF	chr7:147807318-147807353	Lung_OC	lung:	n/a	n/a
23	CTCF	chr7:147807341-147807472	A549	lung:	n/a	n/a
24	CTCF	chr7:147807363-147807406	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr7:147807238-147807563	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:147807291-147807568	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:147807170-147807615	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:147807256-147807545	LNCaP	prostate:	n/a	n/a
29	CTCF	chr7:147807260-147807410	HRE	kidney:	n/a	n/a
30	CTCF	chr7:147807320-147807470	RPTEC	kidney:	n/a	n/a
31	CTCF	chr7:147807420-147807570	HCM	heart:	n/a	n/a
32	CTCF	chr7:147807199-147807686	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:147807353-147807388	ProgFib	skin:	n/a	n/a
34	CTCF	chr7:147807320-147807470	Caco-2	colon:	n/a	n/a
35	CTCF	chr7:147835140-147835290	NHLF	lung:	n/a	n/a
36	CTCF	chr7:147807340-147807490	MCF-7	breast:	n/a	n/a
37	CTCF	chr7:147807297-147807548	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:147807300-147807450	NB4	blood:	n/a	n/a
39	CTCF	chr7:147807267-147807550	T-47D	breast:	n/a	n/a
40	CTCF	chr7:147836833-147836913	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr7:147807340-147807490	AG09309	skin:	n/a	n/a
42	CTCF	chr7:147807340-147807490	HepG2	liver:	n/a	n/a
43	CTCF	chr7:147807320-147807470	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr7:147807380-147807530	GM12875	blood:	n/a	n/a
45	CTCF	chr7:147807280-147807430	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr7:147807277-147807479	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr7:147807302-147807510	HepG2	liver:	n/a	n/a
48	CTCF	chr7:147807374-147807435	GM12878	blood:	n/a	n/a
49	CTCF	chr7:147807298-147807474	K562	blood:	n/a	n/a
50	CTCF	chr7:147807360-147807510	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:147804524-147804574	GM06990	blood:	n/a
2	chr7:147804524-147804574	K562	blood:	n/a
3	chr7:147804524-147804574	PFSK-1	brain:	n/a
4	chr7:147804524-147804574	HCT-116	colon:	n/a
5	chr7:147804524-147804574	HRCEpiC	kidney:	n/a
6	chr7:147804524-147804574	T-47D	breast:	n/a
7	chr7:147804524-147804574	HCF	heart:	n/a
8	chr7:147804524-147804574	RPTEC	kidney:	n/a
9	chr7:147804524-147804574	BE2_C	brain:	n/a
10	chr7:147804524-147804574	A549	lung:	n/a
11	chr7:147804524-147804574	NHBE	bronchial:	n/a
12	chr7:147804524-147804574	PrEC	prostate:	n/a
13	chr7:147804524-147804574	GM12892	blood:	n/a
14	chr7:147804524-147804574	HIPEpiC	eye:	n/a
15	chr7:147804524-147804574	LNCaP	prostate:	n/a
16	chr7:147804524-147804574	GM12891	blood:	n/a
17	chr7:147804524-147804574	SK-N-SH_RA	brain:	n/a
18	chr7:147804524-147804574	SK-N-SH	brain:	n/a
19	chr7:147804524-147804574	SK-N-MC	brain:	n/a
20	chr7:147804524-147804574	SKMC	muscle:	n/a
21	chr7:147804524-147804574	AG10803	skin:	n/a
22	chr7:147804524-147804574	HRPEpiC	eye:	n/a
23	chr7:147804524-147804574	ovcar-3	ovarian:	n/a
24	chr7:147804524-147804574	AG09319	gingival:	n/a
25	chr7:147804524-147804574	IMR90	lung:	fetal
26	chr7:147804524-147804574	NB4	blood:	n/a
27	chr7:147804524-147804574	HEK293	kidney:	embryo
28	chr7:147804524-147804574	ProgFib	skin:	n/a
29	chr7:147804524-147804574	Hela-S3	cervix:	n/a
30	chr7:147804524-147804574	MCF10A-Er-Src	breast:	n/a
31	chr7:147804524-147804574	NT2-D1	testis:	n/a
32	chr7:147804524-147804574	U87	brain:	n/a
33	chr7:147804524-147804574	HUVEC	blood vessel:	n/a
34	chr7:147804524-147804574	HRE	kidney:	n/a
35	chr7:147804524-147804574	HMEC	breast:	n/a
36	chr7:147804524-147804574	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:147804524-147804574	AoSMC	blood vessel:	n/a
38	chr7:147804524-147804574	HAEpiC	amniotic membrane:	n/a
39	chr7:147804524-147804574	GM12878	blood:	n/a
40	chr7:147804524-147804574	Jurkat	blood:	n/a
41	chr7:147804524-147804574	BJ	skin:	n/a
42	chr7:147804524-147804574	AG09309	skin:	n/a
43	chr7:147804524-147804574	HepG2	liver:	n/a
44	chr7:147804524-147804574	CMK	blood:	n/a
45	chr7:147804524-147804574	PANC-1	pancreas:	n/a
46	chr7:147804524-147804574	H1-hESC	embryonic stem cell:	embryo
47	chr7:147804524-147804574	HL-60	blood:	n/a
48	chr7:147804524-147804574	NH-A	brain:	n/a
49	chr7:147804524-147804574	MCF-7	breast:	n/a
50	chr7:147804524-147804574	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:147793900..147797120-chr7:147797974..147800235,3	K562	blood:
2	chr7:147793900..147797120-chr7:147797974..147800235,3	K562	blood:
3	chr7:147806885..147808116-chr7:147939052..147939973,3	MCF-7	breast:
4	chr7:147634284..147636297-chr7:147811524..147814125,2	K562	blood:
5	chr17:57913327..57915370-chr7:147799081..147801913,2	MCF-7	breast:
6	chr7:147818812..147820775-chr7:147844662..147846469,2	K562	blood:
7	chr7:147810650..147813439-chr7:147813807..147816832,3	K562	blood:
8	chr7:147829533..147832185-chr7:147834616..147837591,2	K562	blood:
9	chr7:147806880..147807754-chr7:147839428..147840095,3	MCF-7	breast:
10	chr7:147810650..147813439-chr7:147813807..147816832,3	K562	blood:
11	chr7:147813323..147814981-chr7:147892929..147895557,2	K562	blood:

Variant related genes	Relation type
CNTNAP2	TF binding region
CNTNAP2	CpG island
ENSG00000062716	chromatin interactions
ENSG00000174469	chromatin interactions

Extended variants
information (count: 1690 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1690 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530400848	chr7:147796193-147796194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550556481	chr7:147796201-147796202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs58342445	chr7:147796202-147796203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147667321	chr7:147796205-147796206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546784491	chr7:147796206-147796207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566749611	chr7:147796255-147796256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564522736	chr7:147796263-147796264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35956629	chr7:147796275-147796276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs58733100	chr7:147796285-147796286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs77332094	chr7:147796298-147796299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569555800	chr7:147796343-147796344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140019675	chr7:147796370-147796371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559094930	chr7:147796385-147796386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558756050	chr7:147796421-147796422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78536263	chr7:147796444-147796445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574834964	chr7:147796456-147796457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540757157	chr7:147796506-147796507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553187503	chr7:147796507-147796508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200597904	chr7:147796514-147796515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540410473	chr7:147796517-147796518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57128760	chr7:147796543-147796544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35957905	chr7:147796551-147796552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs58206492	chr7:147796552-147796553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145850254	chr7:147796580-147796581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34117891	chr7:147796583-147796584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573037654	chr7:147796592-147796593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545243181	chr7:147796607-147796608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564982744	chr7:147796630-147796631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77534766	chr7:147796667-147796668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10271245	chr7:147796690-147796691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10271252	chr7:147796702-147796703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543857682	chr7:147796707-147796708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560988040	chr7:147796714-147796715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371173452	chr7:147796721-147796722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529722253	chr7:147796830-147796831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546324953	chr7:147796848-147796849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79550464	chr7:147796923-147796924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75891213	chr7:147796948-147796949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371951897	chr7:147796959-147796960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79308831	chr7:147796960-147796961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs57627955	chr7:147796965-147796966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532541096	chr7:147796981-147796982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552741152	chr7:147796989-147796990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569440188	chr7:147796990-147796991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186466931	chr7:147796996-147796997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10233900	chr7:147797063-147797064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191296720	chr7:147797083-147797084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534199205	chr7:147797097-147797098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182615342	chr7:147797098-147797099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71532714	chr7:147797148-147797149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147792600-147801400	Weak transcription	Brain Angular Gyrus	brain
2	chr7:147800000-147800400	Enhancers	Brain Substantia Nigra	brain
3	chr7:147800000-147801400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr7:147800400-147800600	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr7:147800400-147801400	Weak transcription	Brain Substantia Nigra	brain
6	chr7:147800600-147800800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr7:147800600-147805000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:147800800-147801000	Enhancers	Brain Germinal Matrix	brain
9	chr7:147800800-147803600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr7:147801000-147803200	Weak transcription	Brain Germinal Matrix	brain
11	chr7:147801400-147801800	Enhancers	Brain Angular Gyrus	brain
12	chr7:147801400-147802000	Enhancers	Brain Substantia Nigra	brain
13	chr7:147801400-147804200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:147801800-147813400	Weak transcription	Brain Angular Gyrus	brain
15	chr7:147802000-147803800	Weak transcription	Brain Substantia Nigra	brain
16	chr7:147802000-147804200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr7:147803200-147806200	Enhancers	Brain Germinal Matrix	brain
18	chr7:147803600-147805800	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr7:147803800-147805600	Enhancers	Brain Substantia Nigra	brain
20	chr7:147803800-147805800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:147803800-147805800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:147803800-147805800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr7:147804000-147805600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:147804000-147805800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr7:147804200-147805200	Enhancers	Brain Cingulate Gyrus	brain
26	chr7:147804200-147805600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:147804200-147805800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr7:147804200-147805800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:147804200-147805800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:147804200-147806000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr7:147804400-147804800	Enhancers	Brain Anterior Caudate	brain
32	chr7:147804400-147805000	Enhancers	Fetal Brain Female	brain
33	chr7:147804400-147805600	Enhancers	Brain Hippocampus Middle	brain
34	chr7:147804400-147805800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr7:147804400-147805800	Enhancers	Fetal Brain Male	brain
36	chr7:147804800-147805200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr7:147804800-147805200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr7:147805000-147805200	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr7:147805000-147805600	Weak transcription	Fetal Brain Female	brain
40	chr7:147805000-147805800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr7:147805000-147805800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr7:147805000-147805800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:147805000-147805800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:147805200-147805600	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr7:147805200-147814200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:147805200-147815400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr7:147805200-147817000	Weak transcription	Brain Cingulate Gyrus	brain
48	chr7:147805600-147805800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:147805600-147805800	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr7:147805600-147805800	Enhancers	Fetal Brain Female	brain

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