Variant report

Variant	nsv888758
Chromosome Location	chr7:97050289-97168816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:591)
CpG islands
(count:184)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:97142218-97142424	K562	blood:	n/a	n/a
2	ARID3A	chr7:97079843-97080204	K562	blood:	n/a	n/a
3	ATF1	chr7:97079821-97080180	K562	blood:	n/a	n/a
4	ATF3	chr7:97142143-97142390	K562	blood:	n/a	n/a
5	BACH1	chr7:97141760-97142405	K562	blood:	n/a	chr7:97141939-97141953
6	BATF	chr7:97142136-97142450	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:97136039-97136375	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:97142169-97142494	K562	blood:	n/a	n/a
9	BHLHE40	chr7:97109242-97109273	K562	blood:	n/a	n/a
10	BHLHE40	chr7:97076314-97076607	K562	blood:	n/a	n/a
11	CBX3	chr7:97068948-97069360	K562	blood:	n/a	n/a
12	CBX3	chr7:97068966-97069246	K562	blood:	n/a	n/a
13	CBX3	chr7:97068902-97069413	HCT-116	colon:	n/a	n/a
14	CBX3	chr7:97079806-97080241	K562	blood:	n/a	n/a
15	CBX3	chr7:97068871-97069405	HCT-116	colon:	n/a	n/a
16	CBX3	chr7:97090943-97091222	K562	blood:	n/a	n/a
17	CCNT2	chr7:97079799-97080109	K562	blood:	n/a	n/a
18	CCNT2	chr7:97157423-97157513	K562	blood:	n/a	n/a
19	CEBPB	chr7:97144917-97145196	K562	blood:	n/a	chr7:97145052-97145061
20	CEBPB	chr7:97050690-97051226	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr7:97144399-97145230	K562	blood:	n/a	chr7:97144528-97144541 chr7:97145052-97145061
22	CEBPB	chr7:97081804-97081918	K562	blood:	n/a	n/a
23	CEBPB	chr7:97121986-97122163	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:97079719-97080111	K562	blood:	n/a	n/a
25	CEBPB	chr7:97144930-97145170	K562	blood:	n/a	chr7:97145052-97145061
26	CEBPB	chr7:97142169-97142483	K562	blood:	n/a	n/a
27	CEBPB	chr7:97151488-97151691	A549	lung:	n/a	n/a
28	CEBPB	chr7:97050660-97051183	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPD	chr7:97079682-97080239	K562	blood:	n/a	n/a
30	CEBPD	chr7:97079707-97080212	K562	blood:	n/a	n/a
31	CEBPZ	chr7:97099741-97099747	HepG2	liver:	n/a	n/a
32	CEBPZ	chr7:97069104-97069192	HepG2	liver:	n/a	n/a
33	CHD2	chr7:97088989-97089189	K562	blood:	n/a	n/a
34	CHD2	chr7:97128736-97128744	HepG2	liver:	n/a	n/a
35	CTCF	chr7:97128620-97128770	GM12801	blood:	n/a	n/a
36	CTCF	chr7:97128640-97128790	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr7:97128620-97128802	GM12892	blood:	n/a	n/a
38	CTCF	chr7:97128640-97128790	GM12865	blood:	n/a	n/a
39	CTCF	chr7:97132820-97132970	HepG2	liver:	n/a	n/a
40	CTCF	chr7:97128522-97128910	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:97128660-97128810	GM12872	blood:	n/a	n/a
42	CTCF	chr7:97128451-97129023	HCT-116	colon:	n/a	n/a
43	CTCF	chr7:97128640-97128790	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr7:97128680-97128830	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:97128591-97128849	Medullo	brain:	n/a	n/a
46	CTCF	chr7:97128600-97128750	GM12874	blood:	n/a	n/a
47	CTCF	chr7:97132800-97132950	GM12871	blood:	n/a	n/a
48	CTCF	chr7:97154653-97154668	LNCaP	prostate:	n/a	n/a
49	CTCF	chr7:97128480-97128630	GM12872	blood:	n/a	n/a
50	CTCF	chr7:97098026-97098066	GM10266	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97157869-97157919	SK-N-SH_RA	brain:	n/a
2	chr7:97157869-97157919	SK-N-SH_RA	brain:	n/a
3	chr7:97158782-97158832	GM19239	blood:	n/a
4	chr7:97157869-97157919	CMK	blood:	n/a
5	chr7:97158782-97158832	NB4	blood:	n/a
6	chr7:97158782-97158832	MCF-7	breast:	n/a
7	chr7:97157869-97157919	HUVEC	blood vessel:	n/a
8	chr7:97162175-97162225	AG04449	skin:	fetal
9	chr7:97158782-97158832	T-47D	breast:	n/a
10	chr7:97157869-97157919	NHDF-neo	bronchial:	n/a
11	chr7:97158782-97158832	GM06990	blood:	n/a
12	chr7:97158782-97158832	GM12891	blood:	n/a
13	chr7:97157869-97157919	HCM	heart:	n/a
14	chr7:97162175-97162225	PFSK-1	brain:	n/a
15	chr7:97157869-97157919	HL-60	blood:	n/a
16	chr7:97162175-97162225	GM12878	blood:	n/a
17	chr7:97158782-97158832	PFSK-1	brain:	n/a
18	chr7:97157869-97157919	ProgFib	skin:	n/a
19	chr7:97157869-97157919	BE2_C	brain:	n/a
20	chr7:97157869-97157919	GM06990	blood:	n/a
21	chr7:97157869-97157919	PANC-1	pancreas:	n/a
22	chr7:97158782-97158832	IMR90	lung:	fetal
23	chr7:97162175-97162225	MCF10A-Er-Src	breast:	n/a
24	chr7:97162175-97162225	CMK	blood:	n/a
25	chr7:97157869-97157919	Jurkat	blood:	n/a
26	chr7:97162175-97162225	GM19239	blood:	n/a
27	chr7:97158782-97158832	SAEC	small airway:	n/a
28	chr7:97158782-97158832	AG04450	lung:	fetal
29	chr7:97162175-97162225	IMR90	lung:	fetal
30	chr7:97157869-97157919	HNPCEpiC	eye:	n/a
31	chr7:97158782-97158832	HNPCEpiC	eye:	n/a
32	chr7:97158782-97158832	RPTEC	kidney:	n/a
33	chr7:97157869-97157919	ovcar-3	ovarian:	n/a
34	chr7:97158782-97158832	GM12892	blood:	n/a
35	chr7:97158782-97158832	HEK293	kidney:	embryo
36	chr7:97158782-97158832	PANC-1	pancreas:	n/a
37	chr7:97157869-97157919	MCF10A-Er-Src	breast:	n/a
38	chr7:97158782-97158832	BE2_C	brain:	n/a
39	chr7:97162175-97162225	HRPEpiC	eye:	n/a
40	chr7:97158782-97158832	Hela-S3	cervix:	n/a
41	chr7:97157869-97157919	AG04449	skin:	fetal
42	chr7:97157869-97157919	PFSK-1	brain:	n/a
43	chr7:97162175-97162225	NB4	blood:	n/a
44	chr7:97162175-97162225	HCF	heart:	n/a
45	chr7:97157869-97157919	A549	lung:	n/a
46	chr7:97162175-97162225	HRCEpiC	kidney:	n/a
47	chr7:97162175-97162225	MCF-7	breast:	n/a
48	chr7:97162175-97162225	ovcar-3	ovarian:	n/a
49	chr7:97158782-97158832	AG09319	gingival:	n/a
50	chr7:97162175-97162225	BJ	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97144562..97147344-chr7:97147622..97149562,2	K562	blood:
2	chr7:97150187..97152185-chr7:97153537..97156038,2	K562	blood:
3	chr7:97048782..97050898-chr7:97468212..97470013,2	K562	blood:
4	chr7:97038233..97040741-chr7:97056603..97058477,2	K562	blood:
5	chr7:97049254..97050948-chr7:97055423..97058355,2	K562	blood:
6	chr7:97105914..97108921-chr7:97111052..97113024,3	K562	blood:
7	chr7:97115929..97118142-chr7:97120900..97123183,2	K562	blood:
8	chr5:57754807..57755506-chr7:97052674..97053220,2	Hela-S3	cervix:
9	chr7:97128256..97128858-chr7:97465708..97466442,2	K562	blood:
10	chr7:97150187..97152185-chr7:97153537..97156038,2	K562	blood:
11	chr7:97150187..97153466-chr7:97153537..97156915,4	K562	blood:
12	chr7:97144562..97147344-chr7:97147622..97149562,2	K562	blood:
13	chr7:97103018..97105848-chr7:97107556..97110700,3	K562	blood:
14	chr7:97105914..97108921-chr7:97111052..97113024,3	K562	blood:
15	chr7:97128674..97129320-chr7:97474641..97475573,2	K562	blood:
16	chr7:97103018..97105848-chr7:97107556..97110700,3	K562	blood:
17	chr7:97076230..97078215-chr7:97082351..97084350,2	K562	blood:
18	chr7:97115929..97118142-chr7:97120900..97123183,2	K562	blood:
19	chr6:15954730..15955700-chr7:97086457..97086982,2	MCF-7	breast:
20	chr7:97049254..97050948-chr7:97055423..97058355,2	K562	blood:
21	chr7:97128179..97129179-chr7:97464746..97465556,3	MCF-7	breast:
22	chr7:97128692..97129417-chr7:97464626..97465345,2	MCF-7	breast:
23	chr7:97076230..97078215-chr7:97082351..97084350,2	K562	blood:
24	chr7:97150187..97153466-chr7:97153537..97156915,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000226046	TF binding region
ENSG00000226046	CpG island
ENSG00000145632	chromatin interactions

Extended variants
information (count: 1703 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7779001	chr7:97050289-97050290	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138258995	chr7:97050290-97050291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568886887	chr7:97050307-97050308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534953776	chr7:97050358-97050359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529318762	chr7:97050372-97050373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557715997	chr7:97050383-97050384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574138407	chr7:97050390-97050391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200012210	chr7:97050471-97050472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142850352	chr7:97050492-97050493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115103059	chr7:97050500-97050501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533546710	chr7:97050527-97050528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs5886023	chr7:97050542-97050543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573242260	chr7:97050549-97050550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545105565	chr7:97050578-97050579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564898811	chr7:97050599-97050600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187437682	chr7:97050602-97050603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544078027	chr7:97050634-97050635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114963328	chr7:97050653-97050654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375757174	chr7:97050656-97050657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529848129	chr7:97050686-97050687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546730394	chr7:97050753-97050754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566561762	chr7:97050791-97050792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs992435	chr7:97050803-97050804	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs539208508	chr7:97050812-97050813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs193274290	chr7:97050847-97050848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537876102	chr7:97050877-97050878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75774606	chr7:97050909-97050910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568126368	chr7:97050947-97050948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146077904	chr7:97050952-97050953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184567108	chr7:97050964-97050965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573369626	chr7:97050966-97050967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138872500	chr7:97051064-97051065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149394581	chr7:97051106-97051107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144797768	chr7:97051136-97051137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148579860	chr7:97051167-97051168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561130699	chr7:97051171-97051172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372717123	chr7:97051192-97051193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529961811	chr7:97051223-97051224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540175624	chr7:97051232-97051233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79477333	chr7:97051351-97051352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532377112	chr7:97051398-97051399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113497808	chr7:97051411-97051412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142992930	chr7:97051453-97051454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147349421	chr7:97051472-97051473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569014542	chr7:97051516-97051517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531328966	chr7:97051519-97051520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79426611	chr7:97051522-97051523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567972020	chr7:97051538-97051539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536912995	chr7:97051617-97051618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73708752	chr7:97051646-97051647	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

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
Autism	20858243	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
abnormal development	18461090	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97050000-97051600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:97050000-97052000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:97050200-97052000	Enhancers	Fetal Muscle Leg	muscle
4	chr7:97052000-97055600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:97055600-97056600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:97055600-97056600	Enhancers	Brain Anterior Caudate	brain
7	chr7:97055800-97056600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:97056000-97056400	Enhancers	Brain Germinal Matrix	brain
9	chr7:97056200-97056600	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:97056200-97056600	Enhancers	Brain Hippocampus Middle	brain
11	chr7:97056600-97059400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:97056600-97060400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:97059200-97059600	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr7:97059200-97059600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr7:97059200-97059600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr7:97059400-97059600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:97059400-97059600	Enhancers	Gastric	stomach
18	chr7:97059600-97060000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:97060000-97060800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:97060400-97060600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:97071400-97078600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr7:97075600-97076400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:97075600-97076600	Enhancers	Brain Angular Gyrus	brain
24	chr7:97075600-97076800	Enhancers	Brain Cingulate Gyrus	brain
25	chr7:97075600-97076800	Enhancers	Brain Hippocampus Middle	brain
26	chr7:97075600-97076800	Enhancers	Brain Substantia Nigra	brain
27	chr7:97075600-97077200	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr7:97075800-97076600	Enhancers	Fetal Muscle Leg	muscle
29	chr7:97076200-97076600	Enhancers	K562	blood
30	chr7:97076400-97076800	Enhancers	Brain Anterior Caudate	brain
31	chr7:97076400-97079600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:97076600-97079600	Weak transcription	K562	blood
33	chr7:97079600-97080000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:97079600-97080800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr7:97079600-97081400	Enhancers	K562	blood
36	chr7:97081400-97083400	Weak transcription	K562	blood
37	chr7:97083400-97084400	Enhancers	K562	blood
38	chr7:97086600-97087200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:97094200-97094800	Enhancers	Brain Germinal Matrix	brain
40	chr7:97094600-97094800	Enhancers	Fetal Brain Male	brain
41	chr7:97094800-97098200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:97095200-97095400	Enhancers	Fetal Stomach	stomach
43	chr7:97095200-97095800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:97095200-97096000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:97096000-97097400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:97096400-97096600	Enhancers	Brain Germinal Matrix	brain
47	chr7:97096600-97097000	Enhancers	Fetal Brain Male	brain
48	chr7:97097400-97097600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:97097400-97097800	Enhancers	Fetal Stomach	stomach
50	chr7:97098400-97098800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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