Variant report

Variant	nsv970186
Chromosome Location	chr6:160918235-160932801
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	ARID3A	chr6:160931229-160931590	K562	blood:	n/a	n/a
2	ARID3A	chr6:160928482-160928884	HepG2	liver:	n/a	n/a
3	ATF1	chr6:160927073-160927273	K562	blood:	n/a	n/a
4	ATF1	chr6:160931236-160931585	K562	blood:	n/a	n/a
5	ATF1	chr6:160928438-160928591	K562	blood:	n/a	n/a
6	BACH1	chr6:160931275-160931591	K562	blood:	n/a	n/a
7	BACH1	chr6:160931323-160931490	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr6:160931968-160932306	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:160931382-160931516	K562	blood:	n/a	n/a
10	CCNT2	chr6:160931329-160931529	K562	blood:	n/a	n/a
11	CEBPB	chr6:160928564-160928914	HepG2	liver:	n/a	n/a
12	CEBPB	chr6:160932568-160932717	K562	blood:	n/a	chr6:160932612-160932623 chr6:160932612-160932625
13	CEBPB	chr6:160928636-160928790	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:160932475-160932792	HepG2	liver:	n/a	chr6:160932612-160932623 chr6:160932612-160932625
15	CEBPB	chr6:160932500-160932693	A549	lung:	n/a	chr6:160932612-160932623 chr6:160932612-160932625
16	CHD2	chr6:160928625-160928705	HepG2	liver:	n/a	n/a
17	CREB1	chr6:160921729-160922055	GM12878	blood:	n/a	n/a
18	CTCF	chr6:160932031-160932056	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr6:160921933-160921953	GM20000	blood:	n/a	n/a
20	CTCF	chr6:160932340-160932490	NHLF	lung:	n/a	n/a
21	CTCF	chr6:160920760-160920910	GM12865	blood:	n/a	n/a
22	CTCF	chr6:160927780-160927930	GM12872	blood:	n/a	n/a
23	EP300	chr6:160928580-160928865	HepG2	liver:	n/a	chr6:160928796-160928810
24	EP300	chr6:160928349-160928970	HepG2	liver:	n/a	chr6:160928796-160928810 chr6:160928533-160928540
25	EP300	chr6:160928494-160928703	K562	blood:	n/a	chr6:160928533-160928540
26	EP300	chr6:160931272-160931603	K562	blood:	n/a	n/a
27	FOS	chr6:160926753-160926946	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr6:160926748-160926948	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr6:160931281-160931580	MCF10A-Er-Src	breast:	n/a	chr6:160931421-160931431 chr6:160931420-160931432 chr6:160931421-160931431 chr6:160931422-160931430 chr6:160931421-160931431
30	FOS	chr6:160931265-160931571	MCF10A-Er-Src	breast:	n/a	chr6:160931421-160931431 chr6:160931420-160931432 chr6:160931421-160931431 chr6:160931422-160931430 chr6:160931421-160931431
31	FOS	chr6:160931387-160931561	MCF10A-Er-Src	breast:	n/a	chr6:160931421-160931431 chr6:160931420-160931432 chr6:160931421-160931431 chr6:160931422-160931430 chr6:160931421-160931431
32	FOS	chr6:160931266-160931585	MCF10A-Er-Src	breast:	n/a	chr6:160931421-160931431 chr6:160931420-160931432 chr6:160931421-160931431 chr6:160931422-160931430 chr6:160931421-160931431
33	FOS	chr6:160926759-160926947	MCF10A-Er-Src	breast:	n/a	n/a
34	FOSL2	chr6:160931971-160932224	HepG2	liver:	n/a	n/a
35	FOSL2	chr6:160931902-160932316	HepG2	liver:	n/a	n/a
36	FOXA1	chr6:160928345-160928919	HepG2	liver:	n/a	n/a
37	FOXA1	chr6:160928424-160928930	HepG2	liver:	n/a	n/a
38	FOXA1	chr6:160928342-160928892	HepG2	liver:	n/a	n/a
39	FOXA1	chr6:160928372-160928945	HepG2	liver:	n/a	n/a
40	FOXA1	chr6:160931894-160932267	HepG2	liver:	n/a	n/a
41	FOXA1	chr6:160931949-160932364	HepG2	liver:	n/a	n/a
42	FOXA1	chr6:160931910-160932333	HepG2	liver:	n/a	n/a
43	FOXA1	chr6:160931952-160932263	HepG2	liver:	n/a	n/a
44	FOXA2	chr6:160928393-160928934	HepG2	liver:	n/a	n/a
45	HDAC2	chr6:160928454-160928928	HepG2	liver:	n/a	n/a
46	HEY1	chr6:160931975-160932142	HepG2	liver:	n/a	n/a
47	HEY1	chr6:160931839-160932376	HepG2	liver:	n/a	n/a
48	HNF4A	chr6:160928413-160928859	HepG2	liver:	n/a	chr6:160928704-160928717 chr6:160928703-160928717
49	HNF4A	chr6:160928488-160928845	HepG2	liver:	n/a	chr6:160928704-160928717 chr6:160928703-160928717
50	HNF4A	chr6:160928425-160928893	HepG2	liver:	n/a	chr6:160928704-160928717 chr6:160928703-160928717

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:160932709-160932759	NB4	blood:	n/a
2	chr6:160932709-160932759	NHDF-neo	bronchial:	n/a
3	chr6:160932670-160932720	HCPEpiC	choroid plexus:	n/a
4	chr6:160932670-160932720	ECC-1	luminal epithelium:	n/a
5	chr6:160932670-160932720	NH-A	brain:	n/a
6	chr6:160932670-160932720	HRE	kidney:	n/a
7	chr6:160932670-160932720	PrEC	prostate:	n/a
8	chr6:160932670-160932720	PANC-1	pancreas:	n/a
9	chr6:160932709-160932759	AoSMC	blood vessel:	n/a
10	chr6:160932670-160932720	K562	blood:	n/a
11	chr6:160932709-160932759	ovcar-3	ovarian:	n/a
12	chr6:160932709-160932759	CMK	blood:	n/a
13	chr6:160932709-160932759	HRPEpiC	eye:	n/a
14	chr6:160932670-160932720	HUVEC	blood vessel:	n/a
15	chr6:160932670-160932720	T-47D	breast:	n/a
16	chr6:160932709-160932759	HCM	heart:	n/a
17	chr6:160932670-160932720	HEK293	kidney:	embryo
18	chr6:160932670-160932720	Caco-2	colon:	n/a
19	chr6:160932709-160932759	IMR90	lung:	fetal
20	chr6:160932709-160932759	HNPCEpiC	eye:	n/a
21	chr6:160932670-160932720	MCF10A-Er-Src	breast:	n/a
22	chr6:160932670-160932720	SK-N-SH_RA	brain:	n/a
23	chr6:160932709-160932759	Hela-S3	cervix:	n/a
24	chr6:160932709-160932759	GM06990	blood:	n/a
25	chr6:160932670-160932720	BJ	skin:	n/a
26	chr6:160932670-160932720	HCT-116	colon:	n/a
27	chr6:160932670-160932720	HCF	heart:	n/a
28	chr6:160932670-160932720	H1-hESC	embryonic stem cell:	embryo
29	chr6:160932709-160932759	K562	blood:	n/a
30	chr6:160932709-160932759	Caco-2	colon:	n/a
31	chr6:160932709-160932759	MCF-7	breast:	n/a
32	chr6:160932670-160932720	GM12878	blood:	n/a
33	chr6:160932670-160932720	SAEC	small airway:	n/a
34	chr6:160932709-160932759	AG09319	gingival:	n/a
35	chr6:160932670-160932720	GM19239	blood:	n/a
36	chr6:160932709-160932759	SAEC	small airway:	n/a
37	chr6:160932709-160932759	PANC-1	pancreas:	n/a
38	chr6:160932709-160932759	RPTEC	kidney:	n/a
39	chr6:160932709-160932759	PrEC	prostate:	n/a
40	chr6:160932709-160932759	BE2_C	brain:	n/a
41	chr6:160932709-160932759	ProgFib	skin:	n/a
42	chr6:160932670-160932720	A549	lung:	n/a
43	chr6:160932670-160932720	AoSMC	blood vessel:	n/a
44	chr6:160932709-160932759	BJ	skin:	n/a
45	chr6:160932709-160932759	HepG2	liver:	n/a
46	chr6:160932670-160932720	HL-60	blood:	n/a
47	chr6:160932709-160932759	MCF10A-Er-Src	breast:	n/a
48	chr6:160932709-160932759	SK-N-SH_RA	brain:	n/a
49	chr6:160932709-160932759	U87	brain:	n/a
50	chr6:160932670-160932720	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:160915674..160918470-chr6:160928618..160930503,2	K562	blood:
2	chr6:160919688..160921620-chr6:160926024..160927581,2	K562	blood:
3	chr6:160919688..160921620-chr6:160926024..160927581,2	K562	blood:
4	chr6:160915674..160918470-chr6:160928618..160930503,2	K562	blood:
5	chr6:160918427..160920098-chr6:160939899..160941930,2	K562	blood:

Variant related genes	Relation type
LPAL2	TF binding region
LPAL2	CpG island

Extended variants
information (count: 594 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555855184	chr6:160918257-160918258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552682435	chr6:160918258-160918259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572542763	chr6:160918282-160918283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533745021	chr6:160918283-160918284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7754014	chr6:160918295-160918296	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374860528	chr6:160918343-160918344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186393957	chr6:160918354-160918355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562462315	chr6:160918370-160918371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7754188	chr6:160918414-160918415	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs541467631	chr6:160918462-160918463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561448205	chr6:160918487-160918488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75926289	chr6:160918573-160918574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564667429	chr6:160918580-160918581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7454534	chr6:160918603-160918604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186152980	chr6:160918612-160918613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143610349	chr6:160918638-160918639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533384413	chr6:160918641-160918642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550450794	chr6:160918648-160918649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76076863	chr6:160918671-160918672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535840185	chr6:160918682-160918683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549445518	chr6:160918712-160918713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531627390	chr6:160918714-160918715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147970063	chr6:160918715-160918716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79128870	chr6:160918774-160918775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549786547	chr6:160918777-160918778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576939244	chr6:160918798-160918799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189622411	chr6:160918806-160918807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111711236	chr6:160918820-160918821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75155620	chr6:160918833-160918834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75159081	chr6:160918839-160918840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138843893	chr6:160918868-160918869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571363580	chr6:160918896-160918897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571962628	chr6:160918923-160918924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543938332	chr6:160918940-160918941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75550259	chr6:160918999-160919000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181929069	chr6:160919019-160919020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185918202	chr6:160919044-160919045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7739321	chr6:160919094-160919095	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111844345	chr6:160919144-160919145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10672969	chr6:160919147-160919148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113778935	chr6:160919150-160919151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111454980	chr6:160919151-160919152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112583287	chr6:160919184-160919185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190842079	chr6:160919216-160919217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4129086	chr6:160919223-160919224	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs183156597	chr6:160919306-160919307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528497964	chr6:160919331-160919332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367935391	chr6:160919344-160919345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186471844	chr6:160919353-160919354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571692914	chr6:160919357-160919358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Coronary artery disease	17160897	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Coronary Disease	20032323	CNVD
Coronary Disease	20335594	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160884400-160928200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:160893800-160921800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr6:160893800-160923200	Strong transcription	Liver	Liver
4	chr6:160894800-160923800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:160897800-160923000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr6:160898000-160922800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:160900400-160923400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:160902000-160921000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:160902800-160923000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr6:160903400-160923400	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr6:160903600-160923800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:160903600-160924000	Weak transcription	Brain Hippocampus Middle	brain
13	chr6:160904400-160920600	Weak transcription	Pancreas	Pancrea
14	chr6:160904800-160924000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:160905200-160923000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:160905400-160923400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr6:160905400-160924800	Weak transcription	Ovary	ovary
18	chr6:160908200-160920800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr6:160912000-160924000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr6:160913000-160921000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr6:160913200-160922200	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr6:160913800-160920800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:160914200-160920400	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr6:160914400-160919400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr6:160917200-160918400	Weak transcription	Aorta	Aorta
26	chr6:160918400-160919000	Strong transcription	Aorta	Aorta
27	chr6:160919000-160920600	Weak transcription	Aorta	Aorta
28	chr6:160919400-160922400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr6:160919400-160923000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr6:160920400-160922000	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr6:160920600-160921200	ZNF genes & repeats	Aorta	Aorta
32	chr6:160920600-160921400	Strong transcription	Pancreas	Pancrea
33	chr6:160920800-160921600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:160920800-160921800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr6:160920800-160926600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:160921000-160921400	Strong transcription	H9 Cell Line	embryonic stem cell
37	chr6:160921000-160921800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr6:160921200-160922400	Strong transcription	Aorta	Aorta
39	chr6:160921400-160923400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr6:160921400-160925200	Weak transcription	Pancreas	Pancrea
41	chr6:160921600-160934400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:160921800-160923600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr6:160921800-160924200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:160921800-160924800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr6:160922000-160924600	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr6:160922400-160923800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr6:160922400-160924600	Weak transcription	Aorta	Aorta
48	chr6:160923200-160924200	Weak transcription	Liver	Liver
49	chr6:160923800-160924200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
50	chr6:160924800-160925600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland

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