Variant report

Variant	esv2764033
Chromosome Location	chr7:4121578-4171891
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:1772)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:4170503-4171267	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr7:4143342-4143771	K562	blood:	n/a	n/a
3	CEBPB	chr7:4133326-4133404	K562	blood:	n/a	n/a
4	CEBPB	chr7:4133313-4133359	A549	lung:	n/a	n/a
5	CEBPB	chr7:4143725-4143868	HepG2	liver:	n/a	chr7:4143746-4143757
6	CEBPB	chr7:4164261-4164462	A549	lung:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
7	CEBPB	chr7:4143145-4143844	MCF-7	breast:	n/a	chr7:4143746-4143757
8	CEBPB	chr7:4143283-4143797	A549	lung:	n/a	chr7:4143746-4143757
9	CEBPB	chr7:4143302-4143760	H1-hESC	embryonic stem cell:	n/a	chr7:4143746-4143757
10	CEBPB	chr7:4164281-4164504	HepG2	liver:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
11	CEBPB	chr7:4143335-4143889	K562	blood:	n/a	chr7:4143746-4143757
12	CEBPB	chr7:4170662-4170944	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr7:4143451-4143520	K562	blood:	n/a	n/a
14	CTCF	chr7:4143007-4143365	K562	blood:	n/a	chr7:4143161-4143179
15	CTCF	chr7:4143100-4143250	HepG2	liver:	n/a	chr7:4143161-4143179
16	CTCF	chr7:4143140-4143290	MCF-7	breast:	n/a	chr7:4143161-4143179
17	CTCF	chr7:4143078-4143280	HUVEC	blood vessel:	n/a	chr7:4143161-4143179
18	CTCF	chr7:4169540-4169690	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr7:4170780-4170930	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr7:4143080-4143230	HCT-116	colon:	n/a	chr7:4143161-4143179
21	CTCF	chr7:4170780-4170930	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr7:4143120-4143270	Caco-2	colon:	n/a	chr7:4143161-4143179
23	CTCF	chr7:4143080-4143230	WERI-Rb-1	eye:	n/a	chr7:4143161-4143179
24	CTCF	chr7:4143120-4143270	HUVEC	blood vessel:	n/a	chr7:4143161-4143179
25	CTCF	chr7:4170760-4170910	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:4170780-4170930	HCT-116	colon:	n/a	n/a
27	CTCF	chr7:4143113-4143226	LNCaP	prostate:	n/a	chr7:4143161-4143179
28	CTCF	chr7:4170846-4170874	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:4143079-4143270	LNCaP	prostate:	n/a	chr7:4143161-4143179
30	CTCF	chr7:4170802-4170920	Gliobla	brain:	n/a	n/a
31	CTCF	chr7:4170805-4170916	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr7:4143060-4143210	HCFaa	heart:	n/a	chr7:4143161-4143179
33	CTCF	chr7:4143060-4143210	NHEK	skin:	n/a	chr7:4143161-4143179
34	CTCF	chr7:4143090-4143389	MCF-7	breast:	n/a	chr7:4143161-4143179
35	CTCF	chr7:4143180-4143330	RPTEC	kidney:	n/a	n/a
36	CTCF	chr7:4169520-4169670	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr7:4142880-4143030	HAc	cerebellar:	n/a	n/a
38	CTCF	chr7:4142940-4143090	HRE	kidney:	n/a	n/a
39	CTCF	chr7:4142962-4143587	A549	lung:	n/a	chr7:4143161-4143179
40	CTCF	chr7:4143079-4143289	K562	blood:	n/a	chr7:4143161-4143179
41	CTCF	chr7:4143100-4143250	HPF	lung:	n/a	chr7:4143161-4143179
42	CTCF	chr7:4143134-4143457	Gliobla	brain:	n/a	chr7:4143161-4143179
43	CTCF	chr7:4143092-4143243	HepG2	liver:	n/a	chr7:4143161-4143179
44	CTCF	chr7:4143040-4143190	Caco-2	colon:	n/a	chr7:4143161-4143179
45	CTCF	chr7:4143426-4143437	NHEK	skin:	n/a	n/a
46	CTCF	chr7:4143060-4143210	HCPEpiC	choroid plexus:	n/a	chr7:4143161-4143179
47	CTCF	chr7:4143020-4143170	GM12867	blood:	n/a	n/a
48	CTCF	chr7:4143100-4143250	Hela-S3	cervix:	n/a	chr7:4143161-4143179
49	CTCF	chr7:4143353-4143425	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:4143020-4143170	HMEC	breast:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4167607-4167657	Hela-S3	cervix:	n/a
2	chr7:4153767-4153817	NH-A	brain:	n/a
3	chr7:4170594-4170644	ProgFib	skin:	n/a
4	chr7:4167607-4167657	Hela-S3	cervix:	n/a
5	chr7:4153767-4153817	NH-A	brain:	n/a
6	chr7:4170594-4170644	ProgFib	skin:	n/a
7	chr7:4167411-4167461	HNPCEpiC	eye:	n/a
8	chr7:4169306-4169356	GM12891	blood:	n/a
9	chr7:4146971-4147021	BE2_C	brain:	n/a
10	chr7:4169604-4169654	AG04450	lung:	fetal
11	chr7:4147432-4147482	HNPCEpiC	eye:	n/a
12	chr7:4152976-4153026	SK-N-SH_RA	brain:	n/a
13	chr7:4133359-4133409	HUVEC	blood vessel:	n/a
14	chr7:4150753-4150803	Hela-S3	cervix:	n/a
15	chr7:4133359-4133409	RPTEC	kidney:	n/a
16	chr7:4157691-4157741	AG04449	skin:	fetal
17	chr7:4152976-4153026	NHBE	bronchial:	n/a
18	chr7:4157691-4157741	NT2-D1	testis:	n/a
19	chr7:4167607-4167657	GM12891	blood:	n/a
20	chr7:4169604-4169654	HIPEpiC	eye:	n/a
21	chr7:4147330-4147380	GM12878	blood:	n/a
22	chr7:4147330-4147380	SK-N-SH	brain:	n/a
23	chr7:4157691-4157741	MCF-7	breast:	n/a
24	chr7:4147330-4147380	NHBE	bronchial:	n/a
25	chr7:4170594-4170644	HMEC	breast:	n/a
26	chr7:4153707-4153757	NH-A	brain:	n/a
27	chr7:4170594-4170644	HIPEpiC	eye:	n/a
28	chr7:4147432-4147482	IMR90	lung:	fetal
29	chr7:4147274-4147324	NB4	blood:	n/a
30	chr7:4167809-4167859	PrEC	prostate:	n/a
31	chr7:4167809-4167859	BJ	skin:	n/a
32	chr7:4168039-4168089	K562	blood:	n/a
33	chr7:4153868-4153918	Jurkat	blood:	n/a
34	chr7:4147330-4147380	HRCEpiC	kidney:	n/a
35	chr7:4153732-4153782	HCF	heart:	n/a
36	chr7:4169306-4169356	HCT-116	colon:	n/a
37	chr7:4153767-4153817	AG09309	skin:	n/a
38	chr7:4147330-4147380	PrEC	prostate:	n/a
39	chr7:4167607-4167657	MCF10A-Er-Src	breast:	n/a
40	chr7:4169314-4169364	SAEC	small airway:	n/a
41	chr7:4167607-4167657	ovcar-3	ovarian:	n/a
42	chr7:4153919-4153969	RPTEC	kidney:	n/a
43	chr7:4167809-4167859	PANC-1	pancreas:	n/a
44	chr7:4147432-4147482	ovcar-3	ovarian:	n/a
45	chr7:4146291-4146341	Jurkat	blood:	n/a
46	chr7:4167411-4167461	SK-N-MC	brain:	n/a
47	chr7:4169604-4169654	AG04449	skin:	fetal
48	chr7:4167943-4167993	HRCEpiC	kidney:	n/a
49	chr7:4167809-4167859	GM19239	blood:	n/a
50	chr7:4169306-4169356	AoSMC	blood vessel:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4130773..4135650-chr7:4142053..4144303,4	MCF-7	breast:
2	chr7:4130773..4135650-chr7:4142053..4144303,4	MCF-7	breast:
3	chr7:4126299..4129076-chr7:4130764..4133447,2	K562	blood:
4	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
5	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
6	chr7:4133522..4135936-chr7:4136765..4138658,2	K562	blood:
7	chr7:4133522..4135936-chr7:4136765..4138658,2	K562	blood:
8	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:
9	chr7:4171607..4173163-chr7:4322084..4324253,2	K562	blood:
10	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:
11	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
12	chr7:4126299..4129076-chr7:4130764..4133447,2	K562	blood:

No data

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island

Extended variants
information (count: 2942 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2942 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11979803	chr7:4121578-4121579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377148498	chr7:4121627-4121628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192474807	chr7:4121628-4121629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570590015	chr7:4121630-4121631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370420781	chr7:4121632-4121633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575720684	chr7:4121641-4121642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150512757	chr7:4121647-4121648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367871259	chr7:4121699-4121700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532983868	chr7:4121704-4121705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576206655	chr7:4121710-4121711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139458835	chr7:4121725-4121726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575274583	chr7:4121734-4121735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144566820	chr7:4121785-4121786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11976431	chr7:4121845-4121846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs577410658	chr7:4121854-4121855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546367505	chr7:4121863-4121864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147424923	chr7:4121870-4121871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537842693	chr7:4121871-4121872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185077240	chr7:4121884-4121885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368278758	chr7:4121896-4121897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189061564	chr7:4121937-4121938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561763560	chr7:4121942-4121943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139697819	chr7:4121943-4121944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550826414	chr7:4121974-4121975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112957198	chr7:4121976-4121977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546212861	chr7:4121983-4121984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145248463	chr7:4121986-4121987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564620182	chr7:4121998-4121999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535761612	chr7:4122004-4122005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549280927	chr7:4122005-4122006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144984251	chr7:4122006-4122007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62439623	chr7:4122035-4122036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186802411	chr7:4122100-4122101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62439624	chr7:4122115-4122116	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189717249	chr7:4122128-4122129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74887399	chr7:4122168-4122169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181357268	chr7:4122178-4122179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59285000	chr7:4122193-4122194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs118096993	chr7:4122216-4122217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184987704	chr7:4122241-4122242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575285121	chr7:4122243-4122244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557844780	chr7:4122269-4122270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116881627	chr7:4122277-4122278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs151047106	chr7:4122296-4122297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533472118	chr7:4122304-4122305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141214312	chr7:4122336-4122337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145181605	chr7:4122347-4122348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560421213	chr7:4122398-4122399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529074999	chr7:4122437-4122438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543045293	chr7:4122478-4122479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4088800-4129400	Weak transcription	Right Ventricle	heart
2	chr7:4103000-4125600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:4109600-4122000	Weak transcription	Esophagus	oesophagus
4	chr7:4110200-4129400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr7:4112400-4130200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:4116200-4129200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr7:4117800-4129400	Weak transcription	Fetal Intestine Small	intestine
8	chr7:4118000-4128600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:4118800-4128400	Weak transcription	Aorta	Aorta
10	chr7:4119400-4121600	Weak transcription	Spleen	Spleen
11	chr7:4119400-4153000	Weak transcription	Gastric	stomach
12	chr7:4119600-4125800	Weak transcription	Fetal Stomach	stomach
13	chr7:4119800-4125800	Weak transcription	Pancreas	Pancrea
14	chr7:4120200-4129000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr7:4121000-4125800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:4121200-4121600	Weak transcription	Fetal Brain Male	brain
17	chr7:4121600-4121800	Enhancers	Fetal Brain Male	brain
18	chr7:4121800-4126000	Weak transcription	Fetal Brain Male	brain
19	chr7:4123400-4123600	Weak transcription	Spleen	Spleen
20	chr7:4123800-4124200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:4125400-4126200	Enhancers	Primary B cells from peripheral blood	blood
22	chr7:4125600-4125800	Enhancers	Primary B cells from cord blood	blood
23	chr7:4125600-4126000	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr7:4125600-4126000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:4125600-4126000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:4125600-4126200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
27	chr7:4125600-4126800	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr7:4125800-4126200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:4125800-4126200	ZNF genes & repeats	Fetal Stomach	stomach
30	chr7:4125800-4126400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:4125800-4126800	Strong transcription	Pancreas	Pancrea
32	chr7:4126000-4127800	Enhancers	Fetal Brain Male	brain
33	chr7:4126000-4128600	Weak transcription	Spleen	Spleen
34	chr7:4126200-4126400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:4126200-4126400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:4126200-4126400	Strong transcription	Pancreatic Islets	Pancreatic Islet
37	chr7:4126200-4129200	Weak transcription	Fetal Stomach	stomach
38	chr7:4126400-4126600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:4126400-4130000	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr7:4126600-4128600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:4126800-4128400	Weak transcription	Pancreas	Pancrea
42	chr7:4127800-4130200	Weak transcription	Fetal Brain Male	brain
43	chr7:4128400-4128800	Strong transcription	Aorta	Aorta
44	chr7:4128400-4129000	Strong transcription	Pancreas	Pancrea
45	chr7:4128600-4129200	ZNF genes & repeats	Spleen	Spleen
46	chr7:4128600-4129400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:4128600-4129400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:4128800-4130600	ZNF genes & repeats	Aorta	Aorta
49	chr7:4129000-4129400	ZNF genes & repeats	Pancreas	Pancrea
50	chr7:4129000-4129800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain

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