Variant report

Variant	nsv572977
Chromosome Location	chr16:74873513-74954897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:831)
CpG islands
(count:245)
Chromatin interactive
region (count:57)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:831 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:74896616-74897006	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:74896635-74896965	K562	blood:	n/a	n/a
3	ARID3A	chr16:74902445-74902737	HepG2	liver:	n/a	n/a
4	ATF1	chr16:74896655-74896990	K562	blood:	n/a	n/a
5	ATF2	chr16:74905382-74905951	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr16:74896627-74897029	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr16:74917133-74917384	K562	blood:	n/a	n/a
8	ATF3	chr16:74896603-74896911	K562	blood:	n/a	n/a
9	BACH1	chr16:74905425-74905837	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr16:74908838-74909144	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:74902587-74902752	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr16:74926385-74926742	GM12878	blood:	n/a	n/a
13	BATF	chr16:74926752-74927020	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:74936322-74936458	K562	blood:	n/a	n/a
15	BHLHE40	chr16:74917085-74917559	K562	blood:	n/a	n/a
16	BHLHE40	chr16:74900045-74900264	HepG2	liver:	n/a	n/a
17	BHLHE40	chr16:74926558-74927101	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:74896725-74896978	K562	blood:	n/a	n/a
19	BHLHE40	chr16:74883992-74884175	K562	blood:	n/a	n/a
20	BHLHE40	chr16:74875936-74876280	K562	blood:	n/a	n/a
21	BHLHE40	chr16:74875983-74876148	HepG2	liver:	n/a	n/a
22	CBX3	chr16:74946586-74947207	K562	blood:	n/a	n/a
23	CBX3	chr16:74946817-74947125	K562	blood:	n/a	n/a
24	CEBPB	chr16:74906227-74906573	HepG2	liver:	n/a	chr16:74906408-74906419
25	CEBPB	chr16:74896456-74896885	IMR90	lung:	n/a	chr16:74896733-74896744
26	CEBPB	chr16:74878675-74878757	A549	lung:	n/a	n/a
27	CEBPB	chr16:74877693-74877787	K562	blood:	n/a	n/a
28	CEBPB	chr16:74911707-74911941	K562	blood:	n/a	chr16:74911781-74911792 chr16:74911779-74911796 chr16:74911780-74911793
29	CEBPB	chr16:74881112-74881462	HepG2	liver:	n/a	chr16:74881283-74881294
30	CEBPB	chr16:74896632-74896893	HepG2	liver:	n/a	chr16:74896733-74896744
31	CEBPB	chr16:74906077-74906510	K562	blood:	n/a	chr16:74906408-74906419
32	CEBPB	chr16:74942702-74942955	MCF-7	breast:	n/a	n/a
33	CEBPB	chr16:74936165-74936280	HepG2	liver:	n/a	chr16:74936229-74936242 chr16:74936229-74936240
34	CEBPB	chr16:74874804-74874902	K562	blood:	n/a	chr16:74874833-74874844
35	CEBPB	chr16:74886444-74886718	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr16:74936079-74936395	K562	blood:	n/a	chr16:74936229-74936242 chr16:74936229-74936240
37	CEBPB	chr16:74919248-74919444	K562	blood:	n/a	n/a
38	CEBPB	chr16:74900122-74900189	HepG2	liver:	n/a	n/a
39	CEBPB	chr16:74906235-74906508	IMR90	lung:	n/a	chr16:74906408-74906419
40	CEBPB	chr16:74896426-74897000	Hela-S3	cervix:	n/a	chr16:74896733-74896744
41	CEBPB	chr16:74877578-74877816	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:74930870-74931215	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr16:74911633-74911935	Hela-S3	cervix:	n/a	chr16:74911781-74911792 chr16:74911779-74911796 chr16:74911780-74911793
44	CEBPB	chr16:74881120-74881439	A549	lung:	n/a	chr16:74881283-74881294
45	CEBPB	chr16:74911624-74911959	IMR90	lung:	n/a	chr16:74911781-74911792 chr16:74911779-74911796 chr16:74911780-74911793
46	CEBPB	chr16:74877632-74878013	MCF-7	breast:	n/a	n/a
47	CEBPB	chr16:74911626-74911950	HepG2	liver:	n/a	chr16:74911781-74911792 chr16:74911779-74911796 chr16:74911780-74911793
48	CEBPB	chr16:74953129-74953378	HepG2	liver:	n/a	chr16:74953284-74953295
49	CEBPB	chr16:74877615-74877991	MCF-7	breast:	n/a	n/a
50	CEBPB	chr16:74881148-74881438	Hela-S3	cervix:	n/a	chr16:74881283-74881294

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74904865-74904915	Hepatocyte	liver:	n/a
2	chr16:74904865-74904915	Hepatocyte	liver:	n/a
3	chr16:74904865-74904915	NB4	blood:	n/a
4	chr16:74907756-74907806	HCPEpiC	choroid plexus:	n/a
5	chr16:74919680-74919730	AG04449	skin:	fetal
6	chr16:74919680-74919730	T-47D	breast:	n/a
7	chr16:74901723-74901773	PFSK-1	brain:	n/a
8	chr16:74904865-74904915	AG04450	lung:	fetal
9	chr16:74919680-74919730	IMR90	lung:	fetal
10	chr16:74907756-74907806	H1-hESC	embryonic stem cell:	embryo
11	chr16:74919680-74919730	AG09309	skin:	n/a
12	chr16:74904865-74904915	PANC-1	pancreas:	n/a
13	chr16:74901723-74901773	NHBE	bronchial:	n/a
14	chr16:74919680-74919730	SAEC	small airway:	n/a
15	chr16:74901723-74901773	HRE	kidney:	n/a
16	chr16:74904865-74904915	HCPEpiC	choroid plexus:	n/a
17	chr16:74907756-74907806	HCM	heart:	n/a
18	chr16:74904865-74904915	GM12892	blood:	n/a
19	chr16:74919680-74919730	HMEC	breast:	n/a
20	chr16:74919680-74919730	K562	blood:	n/a
21	chr16:74904865-74904915	IMR90	lung:	fetal
22	chr16:74907756-74907806	RPTEC	kidney:	n/a
23	chr16:74907756-74907806	HRE	kidney:	n/a
24	chr16:74904865-74904915	HEK293	kidney:	embryo
25	chr16:74919680-74919730	HRPEpiC	eye:	n/a
26	chr16:74907756-74907806	Hepatocyte	liver:	n/a
27	chr16:74907756-74907806	NB4	blood:	n/a
28	chr16:74904865-74904915	T-47D	breast:	n/a
29	chr16:74904865-74904915	CMK	blood:	n/a
30	chr16:74904865-74904915	A549	lung:	n/a
31	chr16:74904865-74904915	GM12878	blood:	n/a
32	chr16:74901723-74901773	HEEpiC	esophagus:	n/a
33	chr16:74904865-74904915	HCF	heart:	n/a
34	chr16:74901723-74901773	HRPEpiC	eye:	n/a
35	chr16:74907756-74907806	NHBE	bronchial:	n/a
36	chr16:74907756-74907806	HIPEpiC	eye:	n/a
37	chr16:74919680-74919730	U87	brain:	n/a
38	chr16:74904865-74904915	AoSMC	blood vessel:	n/a
39	chr16:74907756-74907806	ovcar-3	ovarian:	n/a
40	chr16:74907756-74907806	Hela-S3	cervix:	n/a
41	chr16:74901723-74901773	HUVEC	blood vessel:	n/a
42	chr16:74901723-74901773	HEK293	kidney:	embryo
43	chr16:74904865-74904915	HAEpiC	amniotic membrane:	n/a
44	chr16:74919680-74919730	HCF	heart:	n/a
45	chr16:74919680-74919730	RPTEC	kidney:	n/a
46	chr16:74907756-74907806	HAEpiC	amniotic membrane:	n/a
47	chr16:74904865-74904915	K562	blood:	n/a
48	chr16:74904865-74904915	BJ	skin:	n/a
49	chr16:74907756-74907806	GM06990	blood:	n/a
50	chr16:74919680-74919730	HRCEpiC	kidney:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:74908541..74909124-chr16:75144291..75145057,2	MCF-7	breast:
2	chr16:74879689..74881757-chr16:74881968..74884238,2	K562	blood:
3	chr16:74895557..74898464-chr16:74921092..74923999,2	MCF-7	breast:
4	chr16:74920991..74923662-chr16:74926396..74928727,2	MCF-7	breast:
5	chr16:74698032..74700753-chr16:74934562..74936836,2	MCF-7	breast:
6	chr16:74879689..74881757-chr16:74881968..74884238,2	K562	blood:
7	chr16:74877730..74879439-chr16:74879772..74881968,2	MCF-7	breast:
8	chr16:74920873..74922578-chr16:74926256..74928178,2	MCF-7	breast:
9	chr16:74851640..74852331-chr16:74896396..74897214,3	MCF-7	breast:
10	chr16:74935337..74938001-chr16:74940162..74941769,2	K562	blood:
11	chr16:74950852..74952880-chr16:74954374..74957152,3	K562	blood:
12	chr16:74947124..74949915-chr16:74951184..74954053,2	K562	blood:
13	chr16:74742978..74743967-chr16:74896355..74897696,20	MCF-7	breast:
14	chr16:74902093..74904215-chr16:74917294..74919124,2	MCF-7	breast:
15	chr16:74744380..74745053-chr16:74896324..74897155,2	K562	blood:
16	chr16:74950290..74953644-chr16:74954606..74958589,7	MCF-7	breast:
17	chr16:74902093..74904215-chr16:74917294..74919124,2	MCF-7	breast:
18	chr16:74733479..74735052-chr16:74906892..74909261,2	MCF-7	breast:
19	chr16:74743044..74743998-chr16:74896217..74897613,10	K562	blood:
20	chr16:74909348..74911133-chr16:74943622..74945876,2	MCF-7	breast:
21	chr16:74908783..74909343-chr16:75164134..75164687,2	MCF-7	breast:
22	chr16:74877730..74879439-chr16:74879772..74881968,2	MCF-7	breast:
23	chr16:74901214..74902737-chr16:74903278..74906269,2	MCF-7	breast:
24	chr16:74915817..74916666-chr20:9958281..9958987,2	MCF-7	breast:
25	chr16:74800741..74801279-chr16:74896323..74896898,2	K562	blood:
26	chr16:74920211..74922466-chr16:74931010..74932980,2	MCF-7	breast:
27	chr16:74938799..74940789-chr16:74951920..74954706,2	K562	blood:
28	chr16:74932310..74934611-chr16:74935947..74939268,3	K562	blood:
29	chr16:74846723..74847755-chr16:74896368..74897323,9	K562	blood:
30	chr16:74732434..74734727-chr16:74954230..74956473,2	MCF-7	breast:
31	chr16:74938799..74940789-chr16:74951920..74954706,2	K562	blood:
32	chr16:74942655..74944389-chr16:74944724..74947790,3	MCF-7	breast:
33	chr16:74877512..74879263-chr16:74942778..74944341,2	MCF-7	breast:
34	chr16:74846665..74847640-chr16:74896133..74897263,15	MCF-7	breast:
35	chr16:74901214..74902737-chr16:74903278..74906269,2	MCF-7	breast:
36	chr16:74877425..74878040-chr16:74942840..74943385,2	Hela-S3	cervix:
37	chr16:74858744..74860802-chr16:74886371..74889370,2	MCF-7	breast:
38	chr16:74907302..74909892-chr16:74910737..74913353,2	K562	blood:
39	chr16:74743073..74743999-chr16:74894724..74895232,2	MCF-7	breast:
40	chr16:74936501..74938325-chr16:74938873..74941769,2	K562	blood:
41	chr16:74932310..74934611-chr16:74937064..74939268,2	K562	blood:
42	chr16:74942655..74944389-chr16:74944724..74947790,3	MCF-7	breast:
43	chr16:74699239..74702024-chr16:74878313..74880543,2	MCF-7	breast:
44	chr16:74879663..74881841-chr16:74885943..74888600,2	MCF-7	breast:
45	chr16:74948415..74949953-chr16:74950893..74952684,2	K562	blood:
46	chr16:74896697..74898617-chr16:75031619..75033637,2	MCF-7	breast:
47	chr16:74846831..74847572-chr16:74877008..74877733,2	MCF-7	breast:
48	chr16:74743023..74743972-chr16:74896115..74897278,11	MCF-7	breast:
49	chr16:74919621..74922427-chr16:75181112..75183040,2	MCF-7	breast:
50	chr16:74877425..74878040-chr16:74942840..74943385,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNRF1-2	chr16:74905265-74906317	NONHSAT143704

No data

Variant related genes	Relation type
ENSG00000261458	TF binding region
WDR59	TF binding region
ENSG00000261458	CpG island
WDR59	CpG island
ENSG00000103091	chromatin interactions
ENSG00000262904	chromatin interactions
ENSG00000184517	chromatin interactions
ENSG00000168411	chromatin interactions
ENSG00000186187	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000168404	chromatin interactions
ENSG00000247033	chromatin interactions

Extended variants
information (count: 4120 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:4120 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs725710	chr16:74873513-74873514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547054822	chr16:74873527-74873528	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs370568664	chr16:74873528-74873529	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs725709	chr16:74873574-74873575	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs150462157	chr16:74873583-74873584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555886261	chr16:74873600-74873601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138421243	chr16:74873624-74873625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183475539	chr16:74873627-74873628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186616492	chr16:74873654-74873655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572238948	chr16:74873678-74873679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533284038	chr16:74873686-74873687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541241310	chr16:74873698-74873699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148847991	chr16:74873709-74873710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143522057	chr16:74873747-74873748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs137871222	chr16:74873759-74873760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563523002	chr16:74873773-74873774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529291904	chr16:74873820-74873821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192736501	chr16:74873850-74873851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs929883	chr16:74873867-74873868	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs929882	chr16:74873913-74873914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551540951	chr16:74873924-74873925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7190905	chr16:74873927-74873928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs532878126	chr16:74873928-74873929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142387511	chr16:74873934-74873935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569501380	chr16:74873966-74873967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs202116795	chr16:74873967-74873968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377541542	chr16:74874070-74874071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555663373	chr16:74874076-74874077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112272677	chr16:74874077-74874078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58075393	chr16:74874078-74874079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7191282	chr16:74874079-74874080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534944310	chr16:74874081-74874082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113958720	chr16:74874116-74874117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs71378711	chr16:74874125-74874126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35903582	chr16:74874128-74874129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs59459547	chr16:74874146-74874147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543510736	chr16:74874159-74874160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141693151	chr16:74874270-74874271	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs12923955	chr16:74874293-74874294	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs573665552	chr16:74874329-74874330	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs150774791	chr16:74874348-74874349	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs188251939	chr16:74874361-74874362	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs545726412	chr16:74874377-74874378	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs546200016	chr16:74874431-74874432	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs531139219	chr16:74874492-74874493	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs9925233	chr16:74874522-74874523	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs563408838	chr16:74874546-74874547	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs8048847	chr16:74874621-74874622	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs370450592	chr16:74874640-74874641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558436132	chr16:74874684-74874685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Epilepsy	20502679	CNVD
Autism	22495309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2121 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74864800-74877200	Weak transcription	Fetal Intestine Small	intestine
2	chr16:74870600-74877000	Weak transcription	Esophagus	oesophagus
3	chr16:74871400-74876000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr16:74871600-74875800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr16:74871600-74875800	Weak transcription	NHEK	skin
6	chr16:74871600-74876000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr16:74871600-74876000	Weak transcription	HMEC	breast
8	chr16:74872600-74877000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr16:74872800-74877600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr16:74873400-74875200	Weak transcription	Placenta	Placenta
11	chr16:74875200-74875400	Enhancers	Placenta	Placenta
12	chr16:74875400-74875800	Weak transcription	Placenta	Placenta
13	chr16:74875800-74876200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr16:74875800-74877000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:74875800-74877000	Enhancers	Dnd41	blood
16	chr16:74875800-74878400	Enhancers	NHEK	skin
17	chr16:74875800-74879400	Enhancers	Placenta	Placenta
18	chr16:74876000-74876600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr16:74876000-74878000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr16:74876000-74878000	Enhancers	HMEC	breast
21	chr16:74876200-74877800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr16:74876400-74876600	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr16:74876400-74876800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr16:74876600-74878200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr16:74877000-74877200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr16:74877000-74877400	Enhancers	Fetal Intestine Large	intestine
27	chr16:74877000-74877800	Enhancers	Esophagus	oesophagus
28	chr16:74877000-74877800	Flanking Active TSS	Dnd41	blood
29	chr16:74877000-74879200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr16:74877200-74877400	Enhancers	Fetal Intestine Small	intestine
31	chr16:74877200-74877800	Bivalent Enhancer	HepG2	liver
32	chr16:74877400-74880400	Weak transcription	Fetal Intestine Small	intestine
33	chr16:74877600-74878000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr16:74877600-74878000	Enhancers	Hela-S3	cervix
35	chr16:74877800-74878000	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr16:74877800-74878400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr16:74877800-74878400	Enhancers	Dnd41	blood
38	chr16:74878200-74878400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr16:74880200-74881200	Enhancers	GM12878-XiMat	blood
40	chr16:74882800-74883000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr16:74883600-74884400	Enhancers	K562	blood
42	chr16:74883800-74884400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr16:74884000-74905600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr16:74885000-74885800	Enhancers	Duodenum Mucosa	Duodenum
45	chr16:74885000-74885800	Enhancers	Stomach Mucosa	stomach
46	chr16:74885000-74885800	Enhancers	Hela-S3	cervix
47	chr16:74885200-74885400	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr16:74885600-74885800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr16:74885800-74886000	Flanking Active TSS	Hela-S3	cervix
50	chr16:74885800-74886600	Active TSS	Duodenum Mucosa	Duodenum

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