Variant report

Variant	nsv538765
Chromosome Location	chr7:18982862-19021763
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	CBX3	chr7:19017631-19018130	HCT-116	colon:	n/a	n/a
2	CBX3	chr7:19017637-19018234	HCT-116	colon:	n/a	n/a
3	CCNT2	chr7:18990474-18990641	K562	blood:	n/a	n/a
4	CEBPB	chr7:18998188-18998637	IMR90	lung:	n/a	chr7:18998332-18998343
5	CEBPB	chr7:19017663-19018161	HCT-116	colon:	n/a	n/a
6	CEBPB	chr7:19016821-19016980	A549	lung:	n/a	n/a
7	CTCF	chr7:18988920-18989070	GM12873	blood:	n/a	n/a
8	CTCF	chr7:18989020-18989170	BE2_C	brain:	n/a	n/a
9	CTCF	chr7:18988840-18988990	MCF-7	breast:	n/a	n/a
10	CTCF	chr7:18988847-18989059	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr7:18988860-18989010	HEK293	kidney:	n/a	n/a
12	CTCF	chr7:18988880-18989030	GM12875	blood:	n/a	n/a
13	CTCF	chr7:18988800-18988950	GM06990	blood:	n/a	n/a
14	CTCF	chr7:18988840-18988990	GM12871	blood:	n/a	n/a
15	CTCF	chr7:18988920-18989070	NHEK	skin:	n/a	n/a
16	CTCF	chr7:19016740-19016890	AG10803	skin:	n/a	n/a
17	CTCF	chr7:19016540-19016690	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr7:18988920-18989070	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:18988800-18988950	RPTEC	kidney:	n/a	n/a
20	CTCF	chr7:18988945-18989010	Gliobla	brain:	n/a	n/a
21	CTCF	chr7:18988935-18988939	Gliobla	brain:	n/a	n/a
22	CTCF	chr7:19015020-19015170	RPTEC	kidney:	n/a	chr7:19015076-19015086
23	CTCF	chr7:19017767-19017794	GM20000	blood:	n/a	n/a
24	CTCF	chr7:19017796-19017806	GM20000	blood:	n/a	n/a
25	CTCF	chr7:18991840-18991990	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr7:19014900-19015050	RPTEC	kidney:	n/a	n/a
27	CTCF	chr7:19017755-19017764	GM20000	blood:	n/a	n/a
28	CTCF	chr7:18988820-18988970	NHEK	skin:	n/a	n/a
29	CTCF	chr7:18988880-18989030	GM12873	blood:	n/a	n/a
30	CTCF	chr7:18988900-18989050	A549	lung:	n/a	n/a
31	CTCF	chr7:18988860-18989010	HCT-116	colon:	n/a	n/a
32	CTCF	chr7:18988920-18989070	AG09319	gingival:	n/a	n/a
33	CTCF	chr7:19016780-19016930	HPF	lung:	n/a	n/a
34	E2F4	chr7:19017159-19017467	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr7:19017852-19018086	MCF10A-Er-Src	breast:	n/a	n/a
36	EP300	chr7:19001458-19002154	SK-N-SH	brain:	n/a	n/a
37	EP300	chr7:19016902-19018416	SK-N-SH	brain:	n/a	chr7:19018119-19018128 chr7:19017872-19017881 chr7:19017873-19017882
38	EP300	chr7:19001598-19002044	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr7:19014393-19014784	SK-N-SH_RA	brain:	n/a	chr7:19014610-19014619 chr7:19014546-19014556 chr7:19014759-19014773
40	EP300	chr7:19016824-19018440	SK-N-SH	brain:	n/a	chr7:19018119-19018128 chr7:19017872-19017881 chr7:19016879-19016893 chr7:19017873-19017882
41	EP300	chr7:19017009-19018194	SK-N-SH_RA	brain:	n/a	chr7:19018119-19018128 chr7:19017872-19017881 chr7:19017873-19017882
42	EP300	chr7:19016281-19016589	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr7:19017083-19018092	SK-N-SH_RA	brain:	n/a	chr7:19017872-19017881 chr7:19017873-19017882
44	EP300	chr7:19001606-19002013	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr7:19016251-19016668	SK-N-SH_RA	brain:	n/a	n/a
46	FOS	chr7:19017750-19018079	Hela-S3	cervix:	n/a	chr7:19017873-19017881 chr7:19017872-19017881 chr7:19017872-19017882 chr7:19017871-19017882 chr7:19017873-19017880 chr7:19017871-19017883 chr7:19017930-19017941 chr7:19017932-19017940
47	FOS	chr7:19010550-19010750	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr7:19017641-19018186	MCF10A-Er-Src	breast:	n/a	chr7:19017873-19017881 chr7:19017872-19017881 chr7:19017872-19017882 chr7:19017871-19017882 chr7:19017873-19017880 chr7:19017871-19017883 chr7:19017930-19017941 chr7:19017932-19017940
49	FOS	chr7:19012150-19012665	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:19014344-19014925	MCF10A-Er-Src	breast:	n/a	chr7:19014729-19014738 chr7:19014612-19014619 chr7:19014610-19014619 chr7:19014608-19014616

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19018055-19018105	GM12878	blood:	n/a
2	chr7:19018055-19018105	ProgFib	skin:	n/a
3	chr7:19018055-19018105	LNCaP	prostate:	n/a
4	chr7:19018055-19018105	GM19239	blood:	n/a
5	chr7:19018055-19018105	SK-N-SH	brain:	n/a
6	chr7:19018055-19018105	AG10803	skin:	n/a
7	chr7:19018055-19018105	HCT-116	colon:	n/a
8	chr7:19018055-19018105	AG04449	skin:	fetal
9	chr7:19018055-19018105	IMR90	lung:	fetal
10	chr7:19018055-19018105	HEK293	kidney:	embryo
11	chr7:19018055-19018105	AG09319	gingival:	n/a
12	chr7:19018055-19018105	NH-A	brain:	n/a
13	chr7:19018055-19018105	HRPEpiC	eye:	n/a
14	chr7:19018055-19018105	SAEC	small airway:	n/a
15	chr7:19018055-19018105	GM12892	blood:	n/a
16	chr7:19018055-19018105	T-47D	breast:	n/a
17	chr7:19018055-19018105	HEEpiC	esophagus:	n/a
18	chr7:19018055-19018105	Caco-2	colon:	n/a
19	chr7:19018055-19018105	GM06990	blood:	n/a
20	chr7:19018055-19018105	HepG2	liver:	n/a
21	chr7:19018055-19018105	A549	lung:	n/a
22	chr7:19018055-19018105	AoSMC	blood vessel:	n/a
23	chr7:19018055-19018105	HIPEpiC	eye:	n/a
24	chr7:19018055-19018105	Hepatocyte	liver:	n/a
25	chr7:19018055-19018105	Jurkat	blood:	n/a
26	chr7:19018055-19018105	HCF	heart:	n/a
27	chr7:19018055-19018105	PFSK-1	brain:	n/a
28	chr7:19018055-19018105	PANC-1	pancreas:	n/a
29	chr7:19018055-19018105	HCPEpiC	choroid plexus:	n/a
30	chr7:19018055-19018105	U87	brain:	n/a
31	chr7:19018055-19018105	MCF10A-Er-Src	breast:	n/a
32	chr7:19018055-19018105	BE2_C	brain:	n/a
33	chr7:19018055-19018105	SK-N-MC	brain:	n/a
34	chr7:19018055-19018105	HRE	kidney:	n/a
35	chr7:19018055-19018105	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:19018055-19018105	NB4	blood:	n/a
37	chr7:19018055-19018105	HNPCEpiC	eye:	n/a
38	chr7:19018055-19018105	HMEC	breast:	n/a
39	chr7:19018055-19018105	NHBE	bronchial:	n/a
40	chr7:19018055-19018105	HCM	heart:	n/a
41	chr7:19018055-19018105	CMK	blood:	n/a
42	chr7:19018055-19018105	HAEpiC	amniotic membrane:	n/a
43	chr7:19018055-19018105	HUVEC	blood vessel:	n/a
44	chr7:19018055-19018105	AG04450	lung:	fetal
45	chr7:19018055-19018105	BJ	skin:	n/a
46	chr7:19018055-19018105	NT2-D1	testis:	n/a
47	chr7:19018055-19018105	K562	blood:	n/a
48	chr7:19018055-19018105	SK-N-SH_RA	brain:	n/a
49	chr7:19018055-19018105	RPTEC	kidney:	n/a
50	chr7:19018055-19018105	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:19014156..19016996-chr7:19021800..19024663,2	K562	blood:
2	chr7:18996197..18999097-chr7:18999362..19002608,3	K562	blood:
3	chr7:18996197..18999097-chr7:18999362..19002608,3	K562	blood:
4	chr7:18995021..18997746-chr7:19000883..19003609,2	MCF-7	breast:
5	chr7:18995021..18997746-chr7:19000883..19003609,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TWIST1-4	chr7:19006767-19008526	l_3369_chr7:19006113-19008526_breast
2	lnc-TWIST1-4	chr7:19006114-19006397	l_3369_chr7:19006113-19008526_breast
3	lnc-TWIST1-5	chr7:18988521-18989385	NONHSAT119370

Variant related genes	Relation type
NPM1P13	TF binding region
NPM1P13	CpG island

Extended variants
information (count: 1435 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1435 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192532918	chr7:18982878-18982879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562506282	chr7:18982996-18982997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533259660	chr7:18983010-18983011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575810238	chr7:18983031-18983032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375383899	chr7:18983072-18983073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566516572	chr7:18983115-18983116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116025294	chr7:18983134-18983135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546735002	chr7:18983165-18983166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117214146	chr7:18983174-18983175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577000412	chr7:18983176-18983177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539620650	chr7:18983179-18983180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556933934	chr7:18983227-18983228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112335753	chr7:18983235-18983236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546481889	chr7:18983236-18983237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558441717	chr7:18983250-18983251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368680667	chr7:18983305-18983306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139140730	chr7:18983306-18983307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576170710	chr7:18983353-18983354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573329004	chr7:18983416-18983417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540821044	chr7:18983432-18983433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561586188	chr7:18983468-18983469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573769426	chr7:18983506-18983507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544367314	chr7:18983512-18983513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562453690	chr7:18983529-18983530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532974674	chr7:18983543-18983544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114825104	chr7:18983603-18983604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371761812	chr7:18983623-18983624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527455034	chr7:18983728-18983729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183446796	chr7:18983799-18983800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567171126	chr7:18983816-18983817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372911716	chr7:18983817-18983818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17140363	chr7:18983842-18983843	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs144177164	chr7:18983845-18983846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568876813	chr7:18983887-18983888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539468898	chr7:18983888-18983889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187294662	chr7:18983896-18983897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558120483	chr7:18983911-18983912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148694069	chr7:18983922-18983923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561559150	chr7:18983938-18983939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142142985	chr7:18983945-18983946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374813671	chr7:18983961-18983962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374278609	chr7:18983996-18983997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147827319	chr7:18983999-18984000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141638113	chr7:18984020-18984021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544290803	chr7:18984022-18984023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs367930400	chr7:18984047-18984048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145499833	chr7:18984058-18984059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2528409	chr7:18984076-18984077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs28379904	chr7:18984196-18984197	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182071489	chr7:18988205-18988206	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18981200-18983200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:18981400-18983800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:18983800-18984000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:18983800-18984200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:18988200-18988800	Enhancers	Muscle Satellite Cultured Cells	--
6	chr7:18991400-19025000	Weak transcription	Primary B cells from cord blood	blood
7	chr7:18992400-18992800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:18992400-18993600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:18992600-18993400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:18992800-18993800	Enhancers	Fetal Heart	heart
11	chr7:18993600-18994000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:18993800-18994200	Weak transcription	Fetal Heart	heart
13	chr7:18994000-18995000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:18994200-18994400	Enhancers	Fetal Heart	heart
15	chr7:18994400-18997200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr7:18994400-18997600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr7:18994400-19001600	Weak transcription	Fetal Heart	heart
18	chr7:18997000-18997800	Enhancers	Aorta	Aorta
19	chr7:18997000-19005000	Weak transcription	Adipose Nuclei	Adipose
20	chr7:18997600-18997800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:18997600-18998800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:18997600-18998800	Enhancers	NHDF-Ad	bronchial
23	chr7:18997800-18998400	Weak transcription	Aorta	Aorta
24	chr7:18997800-18998800	Enhancers	HSMMtube	muscle
25	chr7:18997800-19000800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:18998000-18998200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:18998000-18998600	Enhancers	Osteobl	bone
28	chr7:18998000-18998800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:18998000-18998800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr7:18998200-18998600	Enhancers	NHEK	skin
31	chr7:18998200-18999400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:18998400-18998600	Enhancers	Aorta	Aorta
33	chr7:18998800-19001400	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr7:18998800-19001400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:18998800-19004600	Weak transcription	NHDF-Ad	bronchial
36	chr7:18998800-19005400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:18999200-18999400	ZNF genes & repeats	HSMM	muscle
38	chr7:18999400-18999600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:18999400-19016400	Weak transcription	HSMM	muscle
40	chr7:18999600-19000400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:19000400-19000600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:19000400-19000800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:19000400-19000800	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:19000400-19001200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr7:19000600-19000800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:19000800-19001000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:19000800-19017600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr7:19001000-19001400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:19001400-19002000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr7:19001400-19002000	Enhancers	Muscle Satellite Cultured Cells	--

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