Variant report

Variant	nsv1021710
Chromosome Location	chr7:12164993-12251790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1036)
CpG islands
(count:796)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12250005-12251450	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:12217799-12218059	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:12211655-12212022	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:12238719-12239430	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:12250389-12250765	K562	blood:	n/a	n/a
6	ARID3A	chr7:12215458-12215671	HepG2	liver:	n/a	n/a
7	ATF1	chr7:12250299-12251081	K562	blood:	n/a	n/a
8	ATF2	chr7:12250697-12251159	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:12250556-12251410	GM12878	blood:	n/a	n/a
10	ATF3	chr7:12250585-12251287	A549	lung:	n/a	n/a
11	ATF3	chr7:12250684-12251031	K562	blood:	n/a	n/a
12	ATF3	chr7:12198233-12198707	A549	lung:	n/a	n/a
13	ATF3	chr7:12250371-12251061	A549	lung:	n/a	n/a
14	BACH1	chr7:12198356-12198454	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr7:12239077-12239359	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:12250927-12251232	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr7:12179134-12179354	GM12878	blood:	n/a	chr7:12179256-12179267
18	BCL3	chr7:12198158-12198741	A549	lung:	n/a	n/a
19	BCL3	chr7:12202244-12202779	A549	lung:	n/a	chr7:12202264-12202273
20	BCL3	chr7:12202048-12202845	A549	lung:	n/a	chr7:12202264-12202273
21	BCL3	chr7:12250386-12251370	A549	lung:	n/a	n/a
22	BCL3	chr7:12250193-12251334	A549	lung:	n/a	n/a
23	BCLAF1	chr7:12250574-12251453	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:12250406-12251283	K562	blood:	n/a	n/a
25	BHLHE40	chr7:12250554-12251415	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:12250424-12251344	HepG2	liver:	n/a	n/a
27	BRCA1	chr7:12227231-12227257	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:12170311-12170630	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr7:12249731-12251347	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:12250424-12250929	HepG2	liver:	n/a	n/a
31	BRCA1	chr7:12178559-12178570	GM12878	blood:	n/a	n/a
32	CBX3	chr7:12250398-12251238	K562	blood:	n/a	n/a
33	CBX3	chr7:12250239-12251446	K562	blood:	n/a	n/a
34	CCNT2	chr7:12250488-12251334	K562	blood:	n/a	chr7:12250905-12250914
35	CEBPB	chr7:12173380-12173913	A549	lung:	n/a	n/a
36	CEBPB	chr7:12215339-12215720	IMR90	lung:	n/a	chr7:12215522-12215533
37	CEBPB	chr7:12238961-12239351	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:12170186-12170403	K562	blood:	n/a	chr7:12170278-12170289
39	CEBPB	chr7:12170142-12170478	A549	lung:	n/a	chr7:12170278-12170289
40	CEBPB	chr7:12215407-12215766	A549	lung:	n/a	chr7:12215522-12215533
41	CEBPB	chr7:12198234-12198738	A549	lung:	n/a	chr7:12198522-12198533
42	CEBPB	chr7:12198319-12198690	IMR90	lung:	n/a	chr7:12198522-12198533
43	CEBPB	chr7:12201697-12202755	Hela-S3	cervix:	n/a	chr7:12202536-12202547
44	CEBPB	chr7:12179116-12179222	K562	blood:	n/a	n/a
45	CEBPB	chr7:12215356-12215694	MCF-7	breast:	n/a	chr7:12215522-12215533
46	CEBPB	chr7:12239001-12239344	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr7:12198367-12198654	HepG2	liver:	n/a	chr7:12198522-12198533
48	CEBPB	chr7:12250312-12251003	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:12170101-12170691	Hela-S3	cervix:	n/a	chr7:12170278-12170289
50	CEBPB	chr7:12217078-12217079	HepG2	liver:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12251200-12251250	SAEC	small airway:	n/a
2	chr7:12250308-12250358	HRPEpiC	eye:	n/a
3	chr7:12250161-12250211	HRPEpiC	eye:	n/a
4	chr7:12251200-12251250	SAEC	small airway:	n/a
5	chr7:12250308-12250358	HRPEpiC	eye:	n/a
6	chr7:12250161-12250211	HRPEpiC	eye:	n/a
7	chr7:12250308-12250358	HRCEpiC	kidney:	n/a
8	chr7:12250760-12250810	HepG2	liver:	n/a
9	chr7:12250390-12250440	SK-N-SH	brain:	n/a
10	chr7:12250390-12250440	AG09309	skin:	n/a
11	chr7:12250161-12250211	HepG2	liver:	n/a
12	chr7:12250308-12250358	GM12878	blood:	n/a
13	chr7:12250760-12250810	HCT-116	colon:	n/a
14	chr7:12250517-12250567	NB4	blood:	n/a
15	chr7:12250760-12250810	AG04449	skin:	fetal
16	chr7:12250938-12250988	Jurkat	blood:	n/a
17	chr7:12250517-12250567	LNCaP	prostate:	n/a
18	chr7:12250857-12250907	PrEC	prostate:	n/a
19	chr7:12250721-12250771	GM12878	blood:	n/a
20	chr7:12250668-12250718	HRPEpiC	eye:	n/a
21	chr7:12250390-12250440	AG04449	skin:	fetal
22	chr7:12250760-12250810	SKMC	muscle:	n/a
23	chr7:12250517-12250567	RPTEC	kidney:	n/a
24	chr7:12251200-12251250	NT2-D1	testis:	n/a
25	chr7:12250161-12250211	AG09309	skin:	n/a
26	chr7:12250938-12250988	HCT-116	colon:	n/a
27	chr7:12250857-12250907	HEEpiC	esophagus:	n/a
28	chr7:12251200-12251250	HIPEpiC	eye:	n/a
29	chr7:12250161-12250211	Hela-S3	cervix:	n/a
30	chr7:12250668-12250718	CMK	blood:	n/a
31	chr7:12250390-12250440	PrEC	prostate:	n/a
32	chr7:12250308-12250358	RPTEC	kidney:	n/a
33	chr7:12250517-12250567	HMEC	breast:	n/a
34	chr7:12250390-12250440	HUVEC	blood vessel:	n/a
35	chr7:12251342-12251392	CMK	blood:	n/a
36	chr7:12250390-12250440	U87	brain:	n/a
37	chr7:12250161-12250211	NHDF-neo	bronchial:	n/a
38	chr7:12250308-12250358	HRE	kidney:	n/a
39	chr7:12250721-12250771	Hela-S3	cervix:	n/a
40	chr7:12250938-12250988	Hela-S3	cervix:	n/a
41	chr7:12250857-12250907	HRPEpiC	eye:	n/a
42	chr7:12250938-12250988	HIPEpiC	eye:	n/a
43	chr7:12247070-12247120	U87	brain:	n/a
44	chr7:12251342-12251392	T-47D	breast:	n/a
45	chr7:12250308-12250358	SAEC	small airway:	n/a
46	chr7:12250938-12250988	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:12250857-12250907	SK-N-SH	brain:	n/a
48	chr7:12228583-12228633	Hela-S3	cervix:	n/a
49	chr7:12250668-12250718	Hepatocyte	liver:	n/a
50	chr7:12250760-12250810	PFSK-1	brain:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:44563231..44563776-chr7:12249962..12250824,2	Hela-S3	cervix:
2	chr7:12237104..12239270-chr7:12329420..12331412,2	K562	blood:
3	chr7:12197065..12199564-chr7:12248019..12250882,2	K562	blood:
4	chr7:12241207..12243591-chr7:12246115..12248890,3	K562	blood:
5	chr17:15554505..15555485-chr7:12250755..12251548,2	Hela-S3	cervix:
6	chr7:12237815..12240381-chr7:12248250..12250812,3	K562	blood:
7	chr7:12245428..12248475-chr7:12248558..12250664,3	K562	blood:
8	chr7:12197794..12199915-chr7:12250140..12252778,2	MCF-7	breast:
9	chr7:12166840..12168760-chr7:12170445..12172889,2	K562	blood:
10	chr7:12193169..12195612-chr7:12198878..12201480,2	K562	blood:
11	chr7:12246346..12248475-chr7:12249160..12251216,3	K562	blood:
12	chr14:39639664..39640469-chr7:12250678..12251257,2	Hela-S3	cervix:
13	chr7:11467204..11469366-chr7:12166192..12168544,2	K562	blood:
14	chr7:12248340..12250610-chr7:12341759..12344659,2	K562	blood:
15	chr7:12166840..12168760-chr7:12170445..12172889,2	K562	blood:
16	chr7:12245428..12248475-chr7:12248558..12250664,3	K562	blood:
17	chr7:12237815..12240381-chr7:12248250..12250812,3	K562	blood:
18	chr7:12241207..12243591-chr7:12246115..12248890,3	K562	blood:
19	chr1:222886239..222887225-chr7:12250816..12251369,2	Hela-S3	cervix:
20	chr7:12225855..12227603-chr7:12250296..12252361,2	K562	blood:
21	chr14:39572252..39573123-chr7:12250595..12251375,2	Hela-S3	cervix:
22	chr7:12170519..12172513-chr7:12174529..12177420,2	K562	blood:
23	chr7:12193169..12195612-chr7:12198878..12201480,2	K562	blood:
24	chr7:12251087..12251775-chr7:12361635..12362202,4	MCF-7	breast:
25	chr7:12251263..12253237-chr7:12442665..12444579,2	K562	blood:
26	chr20:32891034..32891612-chr7:12186432..12186932,2	HCT-116	colon:
27	chr7:12170519..12172513-chr7:12174529..12177420,2	K562	blood:
28	chr7:12250736..12251292-chr9:74383519..74384056,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
TMEM106B	TF binding region
TMEM106B	CpG island
ENSG00000135048	chromatin interactions
ENSG00000100982	chromatin interactions
ENSG00000251537	chromatin interactions
ENSG00000182400	chromatin interactions
ENSG00000146530	chromatin interactions
ENSG00000258651	chromatin interactions
ENSG00000266261	chromatin interactions
ENSG00000162819	chromatin interactions
ENSG00000100934	chromatin interactions
ENSG00000186063	chromatin interactions
ENSG00000106460	chromatin interactions
ENSG00000101444	chromatin interactions

Extended variants
information (count: 3265 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3265 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4719293	chr7:12164993-12164994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552513387	chr7:12165020-12165021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572547032	chr7:12165037-12165038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143498920	chr7:12165038-12165039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543921813	chr7:12165042-12165043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559233710	chr7:12165065-12165066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145165374	chr7:12165111-12165112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17165617	chr7:12165141-12165142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs149113331	chr7:12165167-12165168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574938589	chr7:12165205-12165206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540738745	chr7:12165210-12165211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200634732	chr7:12165256-12165257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573755233	chr7:12165257-12165258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs3079833	chr7:12165270-12165271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142997473	chr7:12165271-12165272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2356057	chr7:12165283-12165284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs144844913	chr7:12165350-12165351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76896850	chr7:12165389-12165390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561307287	chr7:12165390-12165391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2192740	chr7:12165395-12165396	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs375796875	chr7:12165405-12165406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567134882	chr7:12165407-12165408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539095722	chr7:12165408-12165409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535934859	chr7:12165416-12165417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143715247	chr7:12165417-12165418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370041010	chr7:12165448-12165449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79644309	chr7:12165451-12165452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77799645	chr7:12165461-12165462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538659803	chr7:12165472-12165473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188257995	chr7:12165494-12165495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576770061	chr7:12165586-12165587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538157646	chr7:12165589-12165590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192537904	chr7:12165594-12165595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7801081	chr7:12165651-12165652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184924949	chr7:12165702-12165703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555513258	chr7:12165824-12165825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76166662	chr7:12165834-12165835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188151289	chr7:12165842-12165843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138715263	chr7:12165880-12165881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191513578	chr7:12165889-12165890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552324508	chr7:12165916-12165917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544221835	chr7:12165927-12165928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560748240	chr7:12165935-12165936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544131022	chr7:12165942-12165943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529868817	chr7:12165969-12165970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs17165620	chr7:12165986-12165987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs566193935	chr7:12165988-12165989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532127298	chr7:12166042-12166043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78654542	chr7:12166062-12166063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372164345	chr7:12166064-12166065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	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
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Multiple myeloma	17550852	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12163400-12170200	Weak transcription	Hela-S3	cervix
2	chr7:12164400-12166800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr7:12166800-12167200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr7:12166800-12167200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr7:12167000-12167200	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr7:12167000-12167400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr7:12167000-12167400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr7:12167000-12167600	Enhancers	A549	lung
9	chr7:12167200-12170800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr7:12167400-12170400	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr7:12167600-12170600	Weak transcription	A549	lung
12	chr7:12169600-12171400	Enhancers	Fetal Intestine Large	intestine
13	chr7:12169800-12170000	Enhancers	Fetal Intestine Small	intestine
14	chr7:12169800-12170000	Enhancers	Placenta	Placenta
15	chr7:12169800-12171200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr7:12170200-12170800	Enhancers	Hela-S3	cervix
17	chr7:12170400-12171000	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr7:12170400-12171200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:12170400-12171200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr7:12170400-12171200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:12170400-12171400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr7:12170400-12171400	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr7:12170600-12170800	Enhancers	Placenta	Placenta
24	chr7:12170600-12171000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:12170600-12171000	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr7:12170600-12171000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:12170600-12171200	Enhancers	A549	lung
28	chr7:12170800-12171000	Enhancers	Fetal Intestine Small	intestine
29	chr7:12170800-12171200	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr7:12170800-12171200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr7:12170800-12176400	Weak transcription	Hela-S3	cervix
32	chr7:12171200-12173200	Weak transcription	A549	lung
33	chr7:12171200-12173800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr7:12172000-12172200	Weak transcription	Fetal Intestine Small	intestine
35	chr7:12173200-12174000	Enhancers	A549	lung
36	chr7:12173400-12173800	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr7:12173600-12174000	Enhancers	Fetal Kidney	kidney
38	chr7:12173800-12174000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr7:12173800-12174800	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr7:12174000-12176400	Weak transcription	A549	lung
41	chr7:12174200-12174600	Weak transcription	Fetal Intestine Small	intestine
42	chr7:12175000-12175200	Enhancers	Fetal Intestine Small	intestine
43	chr7:12175000-12175200	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr7:12176400-12176600	Enhancers	A549	lung
45	chr7:12176400-12177400	Enhancers	Hela-S3	cervix
46	chr7:12176600-12177000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:12176600-12177000	Flanking Active TSS	A549	lung
48	chr7:12177000-12177200	Enhancers	A549	lung
49	chr7:12177400-12178400	Weak transcription	Hela-S3	cervix
50	chr7:12178000-12180000	Enhancers	NH-A	brain

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