Variant report

Variant	esv1809117
Chromosome Location	chr3:195687670-195717422
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	chr3:195687778-195688031	K562	blood:	n/a	n/a
2	ATF3	chr3:195717067-195717371	A549	lung:	n/a	n/a
3	ATF3	chr3:195717164-195717371	K562	blood:	n/a	n/a
4	ATF3	chr3:195717064-195717382	K562	blood:	n/a	n/a
5	BACH1	chr3:195717045-195717538	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:195716145-195716590	GM12878	blood:	n/a	n/a
7	BATF	chr3:195705475-195705667	GM12878	blood:	n/a	chr3:195705640-195705649 chr3:195705599-195705610
8	BATF	chr3:195715731-195716052	GM12878	blood:	n/a	n/a
9	BATF	chr3:195717279-195717490	GM12878	blood:	n/a	n/a
10	BATF	chr3:195688640-195688926	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:195717225-195717865	GM12878	blood:	n/a	chr3:195717473-195717482
12	BCL11A	chr3:195717296-195717514	GM12878	blood:	n/a	chr3:195717473-195717482
13	BCL11A	chr3:195711556-195711737	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:195716071-195717206	GM12878	blood:	n/a	chr3:195716811-195716824 chr3:195716792-195716801 chr3:195716946-195716959
15	BCL11A	chr3:195715512-195715842	GM12878	blood:	n/a	n/a
16	BCL3	chr3:195700608-195700811	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:195717244-195717251	K562	blood:	n/a	n/a
18	CBX3	chr3:195687930-195689486	K562	blood:	n/a	n/a
19	CBX3	chr3:195717317-195717855	K562	blood:	n/a	n/a
20	CBX3	chr3:195716251-195717942	K562	blood:	n/a	n/a
21	CEBPB	chr3:195715836-195716046	K562	blood:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
22	CEBPB	chr3:195715834-195716053	IMR90	lung:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
23	CEBPB	chr3:195715847-195716034	HepG2	liver:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
24	CEBPB	chr3:195715851-195716051	A549	lung:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
25	CEBPB	chr3:195710856-195710881	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:195715854-195716146	K562	blood:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
27	CEBPB	chr3:195715844-195716052	Hela-S3	cervix:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
28	CEBPB	chr3:195715655-195716331	K562	blood:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
29	CEBPD	chr3:195716979-195717383	HepG2	liver:	n/a	n/a
30	CEBPD	chr3:195716909-195717795	K562	blood:	n/a	n/a
31	CHD2	chr3:195717301-195717419	GM12878	blood:	n/a	n/a
32	CTCF	chr3:195717012-195717039	GM13976	blood:	n/a	n/a
33	CTCF	chr3:195717140-195717290	GM12874	blood:	n/a	n/a
34	CTCF	chr3:195717067-195717671	K562	blood:	n/a	chr3:195717520-195717538
35	CTCF	chr3:195717200-195717350	GM12866	blood:	n/a	n/a
36	CTCF	chr3:195717366-195717594	K562	blood:	n/a	chr3:195717520-195717538
37	CTCF	chr3:195717351-195717551	K562	blood:	n/a	chr3:195717520-195717538
38	CTCF	chr3:195717119-195717280	Lung_OC	lung:	n/a	n/a
39	CTCF	chr3:195717240-195717390	GM12871	blood:	n/a	n/a
40	CTCF	chr3:195717123-195717300	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr3:195705591-195705642	GM13976	blood:	n/a	n/a
42	CTCF	chr3:195716963-195717762	K562	blood:	n/a	chr3:195717520-195717538
43	CTCF	chr3:195717160-195717310	HMEC	breast:	n/a	n/a
44	CTCF	chr3:195707699-195707783	GM13976	blood:	n/a	n/a
45	CTCF	chr3:195717127-195717255	Pancreas_OC	pancreas:	n/a	n/a
46	E2F4	chr3:195710923-195711069	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr3:195717076-195717627	K562	blood:	n/a	chr3:195717225-195717234 chr3:195717274-195717284 chr3:195717347-195717361 chr3:195717277-195717286 chr3:195717495-195717507
48	E2F6	chr3:195717072-195717567	K562	blood:	n/a	chr3:195717225-195717234 chr3:195717274-195717284 chr3:195717347-195717361 chr3:195717277-195717286 chr3:195717495-195717507
49	E2F6	chr3:195717169-195717431	K562	blood:	n/a	chr3:195717225-195717234 chr3:195717274-195717284 chr3:195717347-195717361 chr3:195717277-195717286
50	EBF1	chr3:195690985-195691326	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195717366-195717416	HIPEpiC	eye:	n/a
2	chr3:195703920-195703970	AG10803	skin:	n/a
3	chr3:195717366-195717416	HIPEpiC	eye:	n/a
4	chr3:195703920-195703970	AG10803	skin:	n/a
5	chr3:195703920-195703970	HMEC	breast:	n/a
6	chr3:195714100-195714150	H1-hESC	embryonic stem cell:	embryo
7	chr3:195717366-195717416	SK-N-MC	brain:	n/a
8	chr3:195716626-195716676	HEEpiC	esophagus:	n/a
9	chr3:195716626-195716676	NB4	blood:	n/a
10	chr3:195709698-195709748	GM19239	blood:	n/a
11	chr3:195714100-195714150	NHDF-neo	bronchial:	n/a
12	chr3:195701166-195701216	GM12892	blood:	n/a
13	chr3:195709661-195709711	U87	brain:	n/a
14	chr3:195703920-195703970	Hela-S3	cervix:	n/a
15	chr3:195709661-195709711	HNPCEpiC	eye:	n/a
16	chr3:195716632-195716682	CMK	blood:	n/a
17	chr3:195714100-195714150	HRE	kidney:	n/a
18	chr3:195717416-195717466	Hepatocyte	liver:	n/a
19	chr3:195688021-195688071	GM06990	blood:	n/a
20	chr3:195717344-195717394	HCPEpiC	choroid plexus:	n/a
21	chr3:195688021-195688071	NB4	blood:	n/a
22	chr3:195715851-195715901	BJ	skin:	n/a
23	chr3:195701118-195701168	AG10803	skin:	n/a
24	chr3:195687741-195687791	SKMC	muscle:	n/a
25	chr3:195716626-195716676	AG09319	gingival:	n/a
26	chr3:195716632-195716682	GM19239	blood:	n/a
27	chr3:195709661-195709711	GM12892	blood:	n/a
28	chr3:195688021-195688071	IMR90	lung:	fetal
29	chr3:195688021-195688071	GM12892	blood:	n/a
30	chr3:195687741-195687791	GM12892	blood:	n/a
31	chr3:195716632-195716682	H1-hESC	embryonic stem cell:	embryo
32	chr3:195688021-195688071	HCF	heart:	n/a
33	chr3:195716626-195716676	LNCaP	prostate:	n/a
34	chr3:195716626-195716676	HAEpiC	amniotic membrane:	n/a
35	chr3:195687741-195687791	MCF10A-Er-Src	breast:	n/a
36	chr3:195709661-195709711	K562	blood:	n/a
37	chr3:195709715-195709765	HUVEC	blood vessel:	n/a
38	chr3:195716626-195716676	ECC-1	luminal epithelium:	n/a
39	chr3:195709715-195709765	GM12892	blood:	n/a
40	chr3:195709661-195709711	ProgFib	skin:	n/a
41	chr3:195717416-195717466	T-47D	breast:	n/a
42	chr3:195709715-195709765	SK-N-SH	brain:	n/a
43	chr3:195709698-195709748	AG04449	skin:	fetal
44	chr3:195717366-195717416	HMEC	breast:	n/a
45	chr3:195716632-195716682	HAEpiC	amniotic membrane:	n/a
46	chr3:195717416-195717466	AG10803	skin:	n/a
47	chr3:195700735-195700785	AoSMC	blood vessel:	n/a
48	chr3:195716632-195716682	HCM	heart:	n/a
49	chr3:195709715-195709765	AG09319	gingival:	n/a
50	chr3:195700735-195700785	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:195384346..195385021-chr3:195716746..195717598,2	HCT-116	colon:
2	chr3:195384344..195385079-chr3:195717098..195717747,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-6	chr3:195688656-195689069	expReg_chr3_13675_-

Variant related genes	Relation type
SDHAP1	TF binding region
SDHAP1	CpG island
ENSG00000215837	chromatin interactions
ENSG00000229178	chromatin interactions
ENSG00000242086	chromatin interactions

Extended variants
information (count: 1530 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2620610	chr3:195687670-195687671	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561286915	chr3:195687693-195687694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs62282782	chr3:195687736-195687737	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs185429037	chr3:195687739-195687740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368583456	chr3:195687742-195687743	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2620609	chr3:195687751-195687752	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551085096	chr3:195687772-195687773	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2620608	chr3:195687806-195687807	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs2620607	chr3:195687807-195687808	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549160637	chr3:195687808-195687809	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188228214	chr3:195687838-195687839	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142549538	chr3:195687856-195687857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555873579	chr3:195687870-195687871	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147634491	chr3:195687875-195687876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574230172	chr3:195687882-195687883	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552710872	chr3:195687901-195687902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201491977	chr3:195687913-195687914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369000122	chr3:195687926-195687927	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181424108	chr3:195687927-195687928	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs578168215	chr3:195687935-195687936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs202122483	chr3:195687938-195687939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574985655	chr3:195687971-195687972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186301715	chr3:195687979-195687980	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186733239	chr3:195687982-195687983	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554693211	chr3:195687986-195687987	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141035061	chr3:195688005-195688006	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540489162	chr3:195688008-195688009	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561304322	chr3:195688010-195688011	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565422748	chr3:195688011-195688012	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374631814	chr3:195688021-195688022	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201820092	chr3:195688033-195688034	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150278031	chr3:195688041-195688042	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200580798	chr3:195688045-195688046	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563011725	chr3:195688048-195688049	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201356914	chr3:195688076-195688077	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139345438	chr3:195688106-195688107	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141586514	chr3:195688130-195688131	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561030146	chr3:195688138-195688139	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528280696	chr3:195688141-195688142	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147038037	chr3:195688166-195688167	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571446383	chr3:195688177-195688178	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138244263	chr3:195688183-195688184	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369229975	chr3:195688188-195688189	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538667941	chr3:195688192-195688193	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567389175	chr3:195688196-195688197	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372229685	chr3:195688203-195688204	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374917357	chr3:195688219-195688220	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191617529	chr3:195688220-195688221	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561438301	chr3:195688222-195688223	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373258027	chr3:195688227-195688228	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
2	chr3:195677800-195691800	Weak transcription	NHDF-Ad	bronchial
3	chr3:195678000-195696200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr3:195679000-195691600	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr3:195679000-195695800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:195681600-195691600	Weak transcription	Primary T cells from cord blood	blood
7	chr3:195681600-195696200	Weak transcription	Primary B cells from cord blood	blood
8	chr3:195681800-195688200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:195681800-195688600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr3:195681800-195688800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr3:195681800-195689400	Weak transcription	A549	lung
12	chr3:195681800-195691600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr3:195681800-195691600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr3:195681800-195691600	Weak transcription	Stomach Mucosa	stomach
15	chr3:195681800-195695600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr3:195681800-195696200	Weak transcription	HepG2	liver
17	chr3:195681800-195696400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:195681800-195696400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr3:195681800-195696800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr3:195682000-195691600	Weak transcription	HMEC	breast
21	chr3:195682600-195688000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr3:195682600-195688000	Weak transcription	Hela-S3	cervix
23	chr3:195682600-195689400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr3:195682600-195689400	Weak transcription	Osteobl	bone
25	chr3:195682600-195691600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr3:195682600-195691600	Weak transcription	NHLF	lung
27	chr3:195682600-195693400	Weak transcription	Primary B cells from peripheral blood	blood
28	chr3:195682600-195697000	Weak transcription	Fetal Lung	lung
29	chr3:195682600-195715600	Weak transcription	Psoas Muscle	Psoas
30	chr3:195682800-195688000	Weak transcription	K562	blood
31	chr3:195682800-195688600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:195682800-195689400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr3:195682800-195691000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:195682800-195691600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr3:195682800-195696200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr3:195682800-195696400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr3:195683400-195696600	Weak transcription	HUVEC	blood vessel
38	chr3:195683600-195690400	Strong transcription	Fetal Muscle Trunk	muscle
39	chr3:195683600-195711800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr3:195683800-195696400	Weak transcription	Fetal Brain Male	brain
41	chr3:195684000-195689800	Strong transcription	Fetal Muscle Leg	muscle
42	chr3:195684000-195690200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr3:195684200-195711800	Strong transcription	Placenta	Placenta
44	chr3:195684600-195691600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr3:195685200-195688000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr3:195685400-195688000	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr3:195685400-195690200	Strong transcription	Fetal Brain Female	brain
48	chr3:195685400-195698800	Strong transcription	Dnd41	blood
49	chr3:195685600-195688000	Strong transcription	Pancreas	Pancrea
50	chr3:195685600-195690200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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