Variant report

Variant	nsv877881
Chromosome Location	chr3:163922738-164076198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:427)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:163946376-163946549	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr3:164065590-164065659	K562	blood:	n/a	n/a
3	CEBPB	chr3:163980067-163980373	HepG2	liver:	n/a	chr3:163980184-163980195
4	CEBPB	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
5	CEBPB	chr3:163925893-163926208	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr3:163937094-163937307	K562	blood:	n/a	chr3:163937193-163937204
7	CEBPB	chr3:163937048-163937294	Hela-S3	cervix:	n/a	chr3:163937193-163937204
8	CEBPB	chr3:163961632-163962275	MCF-7	breast:	n/a	chr3:163961848-163961865
9	CEBPB	chr3:163961690-163962327	MCF-7	breast:	n/a	chr3:163961848-163961865
10	CEBPB	chr3:163937023-163937362	A549	lung:	n/a	chr3:163937193-163937204
11	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
12	CEBPB	chr3:163980076-163980312	A549	lung:	n/a	chr3:163980184-163980195
13	CEBPB	chr3:163937041-163937366	HepG2	liver:	n/a	chr3:163937193-163937204
14	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
15	CTBP2	chr3:164038799-164039115	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr3:163953375-163953389	GM10248	blood:	n/a	n/a
17	CTCF	chr3:164050700-164050850	AG09319	gingival:	n/a	n/a
18	CTCF	chr3:164050680-164050830	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr3:164029542-164029558	Lung_OC	lung:	n/a	n/a
20	CTCF	chr3:163926929-163927005	HepG2	liver:	n/a	n/a
21	CTCF	chr3:164050758-164050759	MCF-7	breast:	n/a	n/a
22	CTCF	chr3:163968785-163969078	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
23	CTCF	chr3:164050695-164050869	Medullo	brain:	n/a	n/a
24	CTCF	chr3:164050700-164050850	GM12864	blood:	n/a	n/a
25	CTCF	chr3:163926860-163927010	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:164054702-164054778	GM13976	blood:	n/a	n/a
27	CTCF	chr3:164050720-164050870	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr3:163979232-163979359	K562	blood:	n/a	n/a
29	CTCF	chr3:163926820-163926970	Caco-2	colon:	n/a	n/a
30	CTCF	chr3:163926880-163927030	Caco-2	colon:	n/a	n/a
31	CTCF	chr3:164050660-164050810	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr3:164050700-164050850	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:164050700-164050850	HAc	cerebellar:	n/a	n/a
34	CTCF	chr3:163926954-163927016	Medullo	brain:	n/a	n/a
35	CTCF	chr3:163926820-163926970	HepG2	liver:	n/a	n/a
36	CTCF	chr3:164050520-164050670	Caco-2	colon:	n/a	n/a
37	CTCF	chr3:163968644-163969167	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
38	CTCF	chr3:163926941-163926994	GM13977	blood:	n/a	n/a
39	CTCF	chr3:164050680-164050830	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr3:163926844-163927077	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:164066300-164066450	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:163926863-163927067	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:163926916-163927051	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr3:163968800-163968950	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
45	CTCF	chr3:163926820-163926970	AG09319	gingival:	n/a	n/a
46	CTCF	chr3:163968834-163969001	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
47	CTCF	chr3:163968860-163969010	Caco-2	colon:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
48	CTCF	chr3:163968839-163968974	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
49	CTCF	chr3:164050746-164050829	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:163968800-163968950	RPTEC	kidney:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164059124-164059174	HCF	heart:	n/a
2	chr3:164056463-164056513	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:164050953-164051003	PrEC	prostate:	n/a
4	chr3:164056753-164056803	BE2_C	brain:	n/a
5	chr3:164056463-164056513	GM19239	blood:	n/a
6	chr3:164050953-164051003	HIPEpiC	eye:	n/a
7	chr3:164059011-164059061	HNPCEpiC	eye:	n/a
8	chr3:164050953-164051003	HCF	heart:	n/a
9	chr3:164056463-164056513	RPTEC	kidney:	n/a
10	chr3:164059124-164059174	MCF-7	breast:	n/a
11	chr3:164050953-164051003	HUVEC	blood vessel:	n/a
12	chr3:164009569-164009619	HL-60	blood:	n/a
13	chr3:164059124-164059174	HUVEC	blood vessel:	n/a
14	chr3:164059255-164059305	K562	blood:	n/a
15	chr3:164056753-164056803	HMEC	breast:	n/a
16	chr3:164009569-164009619	NHDF-neo	bronchial:	n/a
17	chr3:164009569-164009619	AG09319	gingival:	n/a
18	chr3:164059124-164059174	A549	lung:	n/a
19	chr3:164050953-164051003	AG09319	gingival:	n/a
20	chr3:164056463-164056513	HepG2	liver:	n/a
21	chr3:164009569-164009619	PANC-1	pancreas:	n/a
22	chr3:164059124-164059174	Hepatocyte	liver:	n/a
23	chr3:164059124-164059174	SK-N-MC	brain:	n/a
24	chr3:164009569-164009619	HRE	kidney:	n/a
25	chr3:164050953-164051003	GM12892	blood:	n/a
26	chr3:164050953-164051003	PANC-1	pancreas:	n/a
27	chr3:164009569-164009619	HAEpiC	amniotic membrane:	n/a
28	chr3:164056463-164056513	NHBE	bronchial:	n/a
29	chr3:164056463-164056513	H1-hESC	embryonic stem cell:	embryo
30	chr3:164056753-164056803	HUVEC	blood vessel:	n/a
31	chr3:164056753-164056803	GM06990	blood:	n/a
32	chr3:164059011-164059061	AG10803	skin:	n/a
33	chr3:164059255-164059305	AG09309	skin:	n/a
34	chr3:164059124-164059174	U87	brain:	n/a
35	chr3:164059011-164059061	HCM	heart:	n/a
36	chr3:164056753-164056803	SAEC	small airway:	n/a
37	chr3:164056753-164056803	HCPEpiC	choroid plexus:	n/a
38	chr3:164056463-164056513	LNCaP	prostate:	n/a
39	chr3:164059011-164059061	HepG2	liver:	n/a
40	chr3:164009569-164009619	H1-hESC	embryonic stem cell:	embryo
41	chr3:164059124-164059174	LNCaP	prostate:	n/a
42	chr3:164056753-164056803	HCT-116	colon:	n/a
43	chr3:164009569-164009619	HMEC	breast:	n/a
44	chr3:164059011-164059061	Hela-S3	cervix:	n/a
45	chr3:164050953-164051003	Hela-S3	cervix:	n/a
46	chr3:164056463-164056513	HEEpiC	esophagus:	n/a
47	chr3:164056753-164056803	SK-N-MC	brain:	n/a
48	chr3:164059011-164059061	LNCaP	prostate:	n/a
49	chr3:164059011-164059061	HEK293	kidney:	embryo
50	chr3:164009569-164009619	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
2	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
3	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
4	chr3:163919977..163922257-chr3:163923536..163925910,2	MCF-7	breast:
5	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
6	chr3:163916797..163919508-chr3:163924219..163927520,3	MCF-7	breast:
7	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
8	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
9	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
10	chr3:164050649..164051226-chr3:164523700..164524566,2	MCF-7	breast:
11	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
12	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:

No data

Variant related genes	Relation type
MIR720	TF binding region
MIR720	CpG island

Extended variants
information (count: 5970 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5970 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1321548	chr3:163922738-163922739	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542687313	chr3:163922769-163922770	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562406264	chr3:163922798-163922799	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576106840	chr3:163922854-163922855	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544828459	chr3:163922909-163922910	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148750185	chr3:163922925-163922926	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142393564	chr3:163922944-163922945	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547334145	chr3:163922956-163922957	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560092678	chr3:163922975-163922976	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529305197	chr3:163923039-163923040	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549374444	chr3:163923071-163923072	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566886582	chr3:163923089-163923090	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569225567	chr3:163923153-163923154	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151309974	chr3:163923173-163923174	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535162335	chr3:163923184-163923185	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569355305	chr3:163923185-163923186	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76314417	chr3:163923193-163923194	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75173581	chr3:163923245-163923246	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534496605	chr3:163923246-163923247	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191777805	chr3:163923273-163923274	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574288453	chr3:163923302-163923303	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574714671	chr3:163923323-163923324	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1449931	chr3:163923355-163923356	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs556126269	chr3:163923358-163923359	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375731386	chr3:163923382-163923383	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552877301	chr3:163923404-163923405	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576011599	chr3:163923452-163923453	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183479762	chr3:163923457-163923458	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564733671	chr3:163923471-163923472	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534254678	chr3:163923486-163923487	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571937236	chr3:163923493-163923494	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558802895	chr3:163923552-163923553	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78814982	chr3:163923577-163923578	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200879688	chr3:163923613-163923614	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560815496	chr3:163923647-163923648	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78508031	chr3:163923651-163923652	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569448322	chr3:163923661-163923662	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190777543	chr3:163923681-163923682	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531705955	chr3:163923704-163923705	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183161407	chr3:163923770-163923771	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74435990	chr3:163923772-163923773	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554707114	chr3:163923790-163923791	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28670723	chr3:163923799-163923800	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186772906	chr3:163923831-163923832	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534382082	chr3:163923860-163923861	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567814233	chr3:163923905-163923906	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11717385	chr3:163923931-163923932	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs577025727	chr3:163923964-163923965	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555874149	chr3:163924029-163924030	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145710049	chr3:163924034-163924035	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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	22032731	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
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Schizophrenia	20967226	CNVD
Acute myeloid leukemia	19651600	CNVD
Autism	19287141	CNVD
Incontinentia Pigmenti	22033527	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163919400-163925600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163925600-163926000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr3:163925600-163926600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:163925800-163927800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr3:163926200-163927400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:163926400-163926800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr3:163926600-163927400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:163926600-163927600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:163926600-163927600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:163926600-163927800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:163926800-163927200	Enhancers	Fetal Brain Male	brain
12	chr3:163926800-163927800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:163927800-163929200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:163929200-163931000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:163931000-163931400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:163931400-163932000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:163932000-163932600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:163932600-163933200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:163933200-163934600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:163934600-163948600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:163938600-163940400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:163939200-163940000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr3:163939200-163940400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:163939200-163940400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:163939600-163940800	Enhancers	Dnd41	blood
26	chr3:163940000-163940400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr3:163940000-163940400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:163940000-163940400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:163946800-163947200	Active TSS	Primary hematopoietic stem cells	blood
30	chr3:163948400-163948800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:163948600-163948800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:163948800-163953000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr3:163948800-163953000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:163952400-163953600	Enhancers	Fetal Kidney	kidney
35	chr3:163953000-163953600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:163953000-163959200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:163953600-163954800	Weak transcription	Fetal Kidney	kidney
38	chr3:163954800-163955600	Enhancers	Fetal Kidney	kidney
39	chr3:163959200-163962000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:163962000-163962600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:163962600-163963200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:163963200-163995200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:163979000-163996200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr3:163982400-163983200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr3:163990800-163993200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr3:163994400-163995200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
47	chr3:163995200-164000600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:163996200-163997000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
49	chr3:164000600-164002200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:164002200-164003000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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