Variant report

Variant	nsv1021056
Chromosome Location	chr7:14162525-14269443
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	CCNT2	chr7:14177038-14177142	K562	blood:	n/a	n/a
2	CEBPB	chr7:14236921-14236993	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:14238195-14238497	HepG2	liver:	n/a	chr7:14238330-14238341
4	CEBPB	chr7:14210612-14210825	MCF-7	breast:	n/a	chr7:14210729-14210738 chr7:14210729-14210738 chr7:14210729-14210738 chr7:14210729-14210738 chr7:14210729-14210740
5	CEBPB	chr7:14250550-14250780	HepG2	liver:	n/a	chr7:14250673-14250684
6	CEBPB	chr7:14186646-14186901	A549	lung:	n/a	n/a
7	CEBPB	chr7:14186722-14186837	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:14186608-14186946	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:14165778-14166126	HepG2	liver:	n/a	chr7:14165982-14165993
10	CEBPB	chr7:14165839-14166083	A549	lung:	n/a	chr7:14165982-14165993
11	CEBPB	chr7:14238227-14238514	IMR90	lung:	n/a	chr7:14238330-14238341
12	CEBPB	chr7:14214129-14214367	HepG2	liver:	n/a	chr7:14214252-14214263
13	CEBPB	chr7:14177318-14177790	HCT-116	colon:	n/a	n/a
14	CEBPB	chr7:14177280-14177733	HCT-116	colon:	n/a	n/a
15	CEBPB	chr7:14210667-14210867	H1-hESC	embryonic stem cell:	n/a	chr7:14210729-14210738 chr7:14210729-14210738 chr7:14210729-14210738 chr7:14210729-14210738 chr7:14210729-14210740
16	CEBPB	chr7:14268697-14269046	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:14186614-14186947	IMR90	lung:	n/a	n/a
18	CTCF	chr7:14165798-14165897	Fibrobl	skin:	n/a	chr7:14165866-14165879
19	CTCF	chr7:14236940-14237090	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr7:14183178-14183338	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr7:14165800-14165950	HRE	kidney:	n/a	chr7:14165866-14165879
22	CTCF	chr7:14183240-14183390	HMF	breast:	n/a	n/a
23	CTCF	chr7:14246640-14246790	RPTEC	kidney:	n/a	n/a
24	CTCF	chr7:14165880-14166030	HEK293	kidney:	n/a	chr7:14165957-14165964 chr7:14165945-14165966
25	CTCF	chr7:14183161-14183355	K562	blood:	n/a	n/a
26	CTCF	chr7:14183240-14183390	RPTEC	kidney:	n/a	n/a
27	CTCF	chr7:14183220-14183370	BE2_C	brain:	n/a	n/a
28	CTCF	chr7:14183240-14183390	HCT-116	colon:	n/a	n/a
29	CTCF	chr7:14233629-14233669	Lung_OC	lung:	n/a	n/a
30	CTCF	chr7:14177880-14178030	BE2_C	brain:	n/a	n/a
31	CTCF	chr7:14165800-14165950	Caco-2	colon:	n/a	chr7:14165866-14165879
32	CTCF	chr7:14165880-14166030	RPTEC	kidney:	n/a	chr7:14165957-14165964 chr7:14165945-14165966
33	CTCF	chr7:14183280-14183430	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr7:14165840-14165990	HBMEC	blood vessel:	n/a	chr7:14165866-14165879 chr7:14165957-14165964 chr7:14165945-14165966
35	CTCF	chr7:14246700-14246850	RPTEC	kidney:	n/a	n/a
36	CTCF	chr7:14247200-14247350	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr7:14165772-14165998	Gliobla	brain:	n/a	chr7:14165866-14165879 chr7:14165957-14165964 chr7:14165945-14165966
38	CTCF	chr7:14165877-14165879	GM12878	blood:	n/a	n/a
39	CTCF	chr7:14229702-14229736	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr7:14183220-14183370	HCT-116	colon:	n/a	n/a
41	CTCF	chr7:14165800-14165950	HCPEpiC	choroid plexus:	n/a	chr7:14165866-14165879
42	CTCF	chr7:14179920-14180070	GM12870	blood:	n/a	n/a
43	CTCF	chr7:14165780-14165930	HCPEpiC	choroid plexus:	n/a	chr7:14165866-14165879
44	CTCF	chr7:14225421-14225474	GM13976	blood:	n/a	n/a
45	CTCF	chr7:14165700-14165990	WI-38	lung:	n/a	chr7:14165866-14165879 chr7:14165957-14165964 chr7:14165945-14165966
46	CTCF	chr7:14165840-14165990	NHEK	skin:	n/a	chr7:14165866-14165879 chr7:14165957-14165964 chr7:14165945-14165966
47	CTCF	chr7:14165800-14165950	AG09319	gingival:	n/a	chr7:14165866-14165879
48	CTCF	chr7:14165800-14165950	AG04450	lung:	n/a	chr7:14165866-14165879
49	CTCF	chr7:14165820-14165970	AG09319	gingival:	n/a	chr7:14165866-14165879 chr7:14165957-14165964 chr7:14165945-14165966
50	CTCF	chr7:14183260-14183410	HPAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:14192484-14192534	SK-N-MC	brain:	n/a
2	chr7:14192484-14192534	NH-A	brain:	n/a
3	chr7:14192484-14192534	MCF-7	breast:	n/a
4	chr7:14188354-14188404	MCF-7	breast:	n/a
5	chr7:14188354-14188404	AG04450	lung:	fetal
6	chr7:14188354-14188404	Hela-S3	cervix:	n/a
7	chr7:14192484-14192534	H1-hESC	embryonic stem cell:	embryo
8	chr7:14192484-14192534	SKMC	muscle:	n/a
9	chr7:14192484-14192534	PFSK-1	brain:	n/a
10	chr7:14192484-14192534	AG10803	skin:	n/a
11	chr7:14188354-14188404	AG10803	skin:	n/a
12	chr7:14192484-14192534	NHBE	bronchial:	n/a
13	chr7:14192484-14192534	SK-N-SH_RA	brain:	n/a
14	chr7:14192484-14192534	K562	blood:	n/a
15	chr7:14188354-14188404	HEK293	kidney:	embryo
16	chr7:14188354-14188404	SK-N-SH	brain:	n/a
17	chr7:14188354-14188404	HRCEpiC	kidney:	n/a
18	chr7:14188354-14188404	CMK	blood:	n/a
19	chr7:14192484-14192534	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:14192484-14192534	BJ	skin:	n/a
21	chr7:14188354-14188404	PrEC	prostate:	n/a
22	chr7:14188354-14188404	PANC-1	pancreas:	n/a
23	chr7:14188354-14188404	HIPEpiC	eye:	n/a
24	chr7:14188354-14188404	NHDF-neo	bronchial:	n/a
25	chr7:14188354-14188404	NB4	blood:	n/a
26	chr7:14188354-14188404	HMEC	breast:	n/a
27	chr7:14188354-14188404	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:14192484-14192534	AG04450	lung:	fetal
29	chr7:14188354-14188404	NHBE	bronchial:	n/a
30	chr7:14188354-14188404	U87	brain:	n/a
31	chr7:14188354-14188404	HCM	heart:	n/a
32	chr7:14188354-14188404	LNCaP	prostate:	n/a
33	chr7:14192484-14192534	HMEC	breast:	n/a
34	chr7:14188354-14188404	HNPCEpiC	eye:	n/a
35	chr7:14188354-14188404	ovcar-3	ovarian:	n/a
36	chr7:14188354-14188404	Hepatocyte	liver:	n/a
37	chr7:14188354-14188404	AG09319	gingival:	n/a
38	chr7:14192484-14192534	HNPCEpiC	eye:	n/a
39	chr7:14188354-14188404	MCF10A-Er-Src	breast:	n/a
40	chr7:14188354-14188404	HRE	kidney:	n/a
41	chr7:14188354-14188404	SK-N-SH_RA	brain:	n/a
42	chr7:14192484-14192534	GM19239	blood:	n/a
43	chr7:14192484-14192534	ProgFib	skin:	n/a
44	chr7:14192484-14192534	GM12891	blood:	n/a
45	chr7:14188354-14188404	NT2-D1	testis:	n/a
46	chr7:14192484-14192534	AoSMC	blood vessel:	n/a
47	chr7:14188354-14188404	GM12891	blood:	n/a
48	chr7:14188354-14188404	AG09309	skin:	n/a
49	chr7:14192484-14192534	NHDF-neo	bronchial:	n/a
50	chr7:14188354-14188404	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:14167244..14169485-chr7:14169676..14171320,2	K562	blood:
2	chr7:14177344..14179951-chr7:14186206..14187901,2	MCF-7	breast:
3	chr7:14188507..14191169-chr7:14194873..14196995,2	MCF-7	breast:
4	chr7:14211165..14212697-chr7:14216006..14218417,2	K562	blood:
5	chr7:14188507..14191169-chr7:14194873..14196995,2	MCF-7	breast:
6	chr7:14211165..14212697-chr7:14216006..14218417,2	K562	blood:
7	chr7:14167244..14169485-chr7:14169676..14171320,2	K562	blood:
8	chr7:14177344..14179951-chr7:14186206..14187901,2	MCF-7	breast:

Variant related genes	Relation type
EEF1A1P26	TF binding region
EEF1A1P26	CpG island

Extended variants
information (count: 3138 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3138 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4721304	chr7:14162525-14162526	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529844375	chr7:14162544-14162545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113651444	chr7:14162553-14162554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372031227	chr7:14162557-14162558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141713124	chr7:14162573-14162574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184389040	chr7:14162586-14162587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531277145	chr7:14162592-14162593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145467871	chr7:14162683-14162684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567817248	chr7:14162739-14162740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536890136	chr7:14162745-14162746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553701391	chr7:14162770-14162771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567081933	chr7:14162786-14162787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77769139	chr7:14162864-14162865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76986811	chr7:14162881-14162882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35072209	chr7:14162893-14162894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371788417	chr7:14162942-14162943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149536943	chr7:14162946-14162947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576713960	chr7:14162979-14162980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575617802	chr7:14163019-14163020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574444226	chr7:14163021-14163022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544253749	chr7:14163070-14163071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs973954	chr7:14163112-14163113	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs540065544	chr7:14163155-14163156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144232071	chr7:14163166-14163167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577025894	chr7:14163195-14163196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546100037	chr7:14163203-14163204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs62454472	chr7:14163211-14163212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189315884	chr7:14163260-14163261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182204966	chr7:14163293-14163294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560812663	chr7:14163336-14163337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369127389	chr7:14163372-14163373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148727863	chr7:14163380-14163381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561812992	chr7:14163384-14163385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143093887	chr7:14163414-14163415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184621601	chr7:14163418-14163419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567072582	chr7:14163435-14163436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189068770	chr7:14163460-14163461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147490824	chr7:14163551-14163552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569118220	chr7:14163568-14163569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371776717	chr7:14163621-14163622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543127360	chr7:14163624-14163625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181502058	chr7:14163635-14163636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376778176	chr7:14163696-14163697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376232655	chr7:14163742-14163743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537893537	chr7:14163752-14163753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554619461	chr7:14163829-14163830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185645744	chr7:14163837-14163838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534040862	chr7:14163913-14163914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371026396	chr7:14163947-14163948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191186264	chr7:14164017-14164018	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14162400-14166200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr7:14162800-14166000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:14163600-14165200	Enhancers	Fetal Brain Male	brain
4	chr7:14164400-14164600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:14164400-14164800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:14164600-14165400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:14164600-14165800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:14165200-14166000	Enhancers	Gastric	stomach
9	chr7:14165400-14166000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:14181800-14185800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr7:14183600-14184400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr7:14184000-14184400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:14184000-14184400	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr7:14184000-14184600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr7:14184200-14184400	Enhancers	Brain Germinal Matrix	brain
16	chr7:14184400-14185600	Weak transcription	Brain Germinal Matrix	brain
17	chr7:14185600-14185800	Enhancers	Brain Germinal Matrix	brain
18	chr7:14185800-14186400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr7:14185800-14186600	Weak transcription	Brain Germinal Matrix	brain
20	chr7:14186400-14188800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr7:14186600-14187200	Enhancers	Brain Germinal Matrix	brain
22	chr7:14187000-14187600	Enhancers	Fetal Brain Female	brain
23	chr7:14188800-14189000	Enhancers	Brain Germinal Matrix	brain
24	chr7:14188800-14189800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:14189200-14192000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:14190600-14191400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr7:14191400-14191600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:14191400-14193800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:14191600-14193000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr7:14192200-14193600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:14192400-14193800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:14192600-14193400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:14192600-14193600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:14192800-14193200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:14193000-14193400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:14193000-14193400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr7:14197200-14198000	Enhancers	Fetal Intestine Large	intestine
38	chr7:14210400-14210600	Enhancers	Right Atrium	heart
39	chr7:14211000-14213000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:14211600-14212200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr7:14217800-14218000	Enhancers	Fetal Brain Male	brain
42	chr7:14218000-14219000	Weak transcription	Fetal Brain Male	brain
43	chr7:14218200-14220400	Enhancers	Fetal Brain Female	brain
44	chr7:14218800-14219800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr7:14219000-14220400	Enhancers	Fetal Brain Male	brain
46	chr7:14220400-14222600	Weak transcription	Fetal Brain Male	brain
47	chr7:14220400-14222800	Weak transcription	Fetal Brain Female	brain
48	chr7:14222200-14222600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:14222400-14223200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:14222600-14223200	Enhancers	Fetal Brain Male	brain

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