Variant report

Variant	nsv906954
Chromosome Location	chr16:77197633-77227180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1179)
CpG islands
(count:732)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:77224078-77225335	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:77225046-77225292	K562	blood:	n/a	n/a
3	ARID3A	chr16:77205725-77206008	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:77224508-77224833	K562	blood:	n/a	n/a
5	ATF1	chr16:77225513-77225821	K562	blood:	n/a	n/a
6	ATF1	chr16:77224488-77225291	K562	blood:	n/a	n/a
7	ATF2	chr16:77224374-77224922	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr16:77225510-77225842	GM12878	blood:	n/a	n/a
9	ATF2	chr16:77224357-77225198	GM12878	blood:	n/a	n/a
10	ATF2	chr16:77224773-77225150	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr16:77224747-77225140	GM12878	blood:	n/a	n/a
12	ATF3	chr16:77214221-77214506	K562	blood:	n/a	n/a
13	BACH1	chr16:77224358-77224813	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr16:77224238-77225319	A549	lung:	n/a	chr16:77225024-77225033 chr16:77225082-77225091 chr16:77225053-77225062
15	BCLAF1	chr16:77224692-77225304	GM12878	blood:	n/a	chr16:77225024-77225033 chr16:77225082-77225091 chr16:77225053-77225062
16	BCLAF1	chr16:77224746-77225325	GM12878	blood:	n/a	chr16:77225024-77225033 chr16:77225082-77225091 chr16:77225053-77225062
17	BHLHE40	chr16:77224414-77225224	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:77205326-77205369	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:77224113-77225697	K562	blood:	n/a	n/a
20	BHLHE40	chr16:77204724-77205046	K562	blood:	n/a	chr16:77204898-77204907 chr16:77204892-77204913 chr16:77204898-77204907 chr16:77204896-77204909 chr16:77204897-77204906
21	BHLHE40	chr16:77223953-77224047	GM12878	blood:	n/a	n/a
22	BHLHE40	chr16:77203460-77203854	K562	blood:	n/a	n/a
23	BHLHE40	chr16:77198470-77198554	GM12878	blood:	n/a	n/a
24	BHLHE40	chr16:77204851-77204939	GM12878	blood:	n/a	chr16:77204898-77204907 chr16:77204892-77204913 chr16:77204898-77204907 chr16:77204896-77204909 chr16:77204897-77204906
25	BRCA1	chr16:77224357-77224617	GM12878	blood:	n/a	n/a
26	BRCA1	chr16:77224076-77224146	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr16:77224402-77225318	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr16:77224552-77225152	HepG2	liver:	n/a	n/a
29	BRCA1	chr16:77203705-77203791	HepG2	liver:	n/a	n/a
30	CBX3	chr16:77225274-77225881	K562	blood:	n/a	n/a
31	CBX3	chr16:77224306-77225239	K562	blood:	n/a	n/a
32	CCNT2	chr16:77224218-77225412	K562	blood:	n/a	n/a
33	CEBPB	chr16:77224363-77224813	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr16:77224415-77225227	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr16:77217151-77217377	A549	lung:	n/a	n/a
36	CEBPB	chr16:77214190-77214865	K562	blood:	n/a	chr16:77214394-77214405
37	CEBPB	chr16:77224338-77225221	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:77224355-77225249	K562	blood:	n/a	n/a
39	CEBPB	chr16:77224130-77225277	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr16:77224206-77225382	A549	lung:	n/a	n/a
41	CEBPB	chr16:77216988-77217453	A549	lung:	n/a	n/a
42	CEBPB	chr16:77224419-77224727	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr16:77224253-77225273	HepG2	liver:	n/a	n/a
44	CEBPB	chr16:77224205-77225176	MCF-7	breast:	n/a	n/a
45	CEBPB	chr16:77224380-77225201	K562	blood:	n/a	n/a
46	CEBPB	chr16:77224284-77225168	A549	lung:	n/a	n/a
47	CEBPB	chr16:77210761-77210886	IMR90	lung:	n/a	chr16:77210783-77210794 chr16:77210781-77210794 chr16:77210781-77210792 chr16:77210783-77210792
48	CEBPB	chr16:77224290-77225291	MCF-7	breast:	n/a	n/a
49	CEBPB	chr16:77205253-77205460	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:77224339-77224758	HepG2	liver:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:77224073-77224123	HCM	heart:	n/a
2	chr16:77221668-77221718	RPTEC	kidney:	n/a
3	chr16:77224401-77224451	SK-N-SH	brain:	n/a
4	chr16:77221668-77221718	HRCEpiC	kidney:	n/a
5	chr16:77224772-77224822	H1-hESC	embryonic stem cell:	embryo
6	chr16:77224808-77224858	HEEpiC	esophagus:	n/a
7	chr16:77224286-77224336	HPAEpiC	pulmonary alveolar:	n/a
8	chr16:77224636-77224686	NHBE	bronchial:	n/a
9	chr16:77224291-77224341	HAEpiC	amniotic membrane:	n/a
10	chr16:77224401-77224451	GM12878	blood:	n/a
11	chr16:77224772-77224822	RPTEC	kidney:	n/a
12	chr16:77224772-77224822	AG09309	skin:	n/a
13	chr16:77224291-77224341	SKMC	muscle:	n/a
14	chr16:77224286-77224336	NT2-D1	testis:	n/a
15	chr16:77224401-77224451	PANC-1	pancreas:	n/a
16	chr16:77221668-77221718	AoSMC	blood vessel:	n/a
17	chr16:77224772-77224822	HEEpiC	esophagus:	n/a
18	chr16:77226774-77226824	NHDF-neo	bronchial:	n/a
19	chr16:77224772-77224822	HCT-116	colon:	n/a
20	chr16:77224808-77224858	Jurkat	blood:	n/a
21	chr16:77224808-77224858	HIPEpiC	eye:	n/a
22	chr16:77221668-77221718	SKMC	muscle:	n/a
23	chr16:77224291-77224341	HIPEpiC	eye:	n/a
24	chr16:77224808-77224858	ProgFib	skin:	n/a
25	chr16:77225049-77225099	ECC-1	luminal epithelium:	n/a
26	chr16:77224291-77224341	NT2-D1	testis:	n/a
27	chr16:77224198-77224248	HUVEC	blood vessel:	n/a
28	chr16:77224286-77224336	PANC-1	pancreas:	n/a
29	chr16:77224286-77224336	BE2_C	brain:	n/a
30	chr16:77224286-77224336	RPTEC	kidney:	n/a
31	chr16:77224073-77224123	SK-N-SH	brain:	n/a
32	chr16:77224198-77224248	HepG2	liver:	n/a
33	chr16:77224198-77224248	BE2_C	brain:	n/a
34	chr16:77225204-77225254	HepG2	liver:	n/a
35	chr16:77224401-77224451	U87	brain:	n/a
36	chr16:77224772-77224822	LNCaP	prostate:	n/a
37	chr16:77221668-77221718	GM12892	blood:	n/a
38	chr16:77224636-77224686	A549	lung:	n/a
39	chr16:77224291-77224341	GM12878	blood:	n/a
40	chr16:77224198-77224248	GM12892	blood:	n/a
41	chr16:77224286-77224336	MCF-7	breast:	n/a
42	chr16:77221668-77221718	Jurkat	blood:	n/a
43	chr16:77224291-77224341	A549	lung:	n/a
44	chr16:77224636-77224686	AG10803	skin:	n/a
45	chr16:77225204-77225254	Jurkat	blood:	n/a
46	chr16:77224636-77224686	HPAEpiC	pulmonary alveolar:	n/a
47	chr16:77224808-77224858	SK-N-SH	brain:	n/a
48	chr16:77224286-77224336	SK-N-MC	brain:	n/a
49	chr16:77225204-77225254	HMEC	breast:	n/a
50	chr16:77224073-77224123	PFSK-1	brain:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:77219312..77221017-chr16:77223275..77224910,2	K562	blood:
2	chr16:77214025..77215535-chr16:77223409..77226145,2	K562	blood:
3	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
4	chr12:46121915..46124342-chr16:77224976..77226839,2	K562	blood:
5	chr16:76887394..76888672-chr16:77203188..77204165,5	MCF-7	breast:
6	chr16:77223534..77226455-chr16:77227601..77231752,9	MCF-7	breast:
7	chr16:77224879..77225863-chr4:151936610..151937513,2	Hela-S3	cervix:
8	chr12:123011094..123011689-chr16:77225072..77225582,2	Hela-S3	cervix:
9	chr16:77223923..77226639-chr16:77244818..77248823,8	K562	blood:
10	chr16:76313028..76313530-chr16:77203611..77204279,2	MCF-7	breast:
11	chr16:76312786..76313346-chr16:77205382..77206025,2	MCF-7	breast:
12	chr16:75823072..75823718-chr16:77205249..77205759,2	MCF-7	breast:
13	chr16:77219105..77221826-chr16:77222885..77224694,2	MCF-7	breast:
14	chr16:77217047..77218852-chr16:77220836..77222789,2	K562	blood:
15	chr16:77078662..77079429-chr16:77203303..77204211,3	MCF-7	breast:
16	chr16:77195182..77197439-chr16:77199216..77201084,2	K562	blood:
17	chr16:77206067..77208430-chr16:77215088..77217473,2	MCF-7	breast:
18	chr16:77223967..77224641-chr17:45908278..45909133,2	Hela-S3	cervix:
19	chr16:75497933..75499469-chr16:77204517..77206368,2	MCF-7	breast:
20	chr16:77216325..77218359-chr16:77222918..77225475,2	MCF-7	breast:
21	chr16:77076688..77077729-chr16:77203577..77204202,3	MCF-7	breast:
22	chr16:77199154..77201257-chr16:77223059..77224570,2	K562	blood:
23	chr16:77223216..77226884-chr16:77251990..77255920,6	MCF-7	breast:
24	chr16:77223598..77226407-chr16:77245076..77246907,2	MCF-7	breast:
25	chr16:77224416..77225113-chr9:131940115..131940671,2	Hela-S3	cervix:
26	chr16:75835360..75835894-chr16:77203310..77204256,2	K562	blood:
27	chr16:77217047..77218852-chr16:77220836..77222789,2	K562	blood:
28	chr16:77224814..77227187-chr16:77245098..77247161,3	K562	blood:
29	chr16:77199154..77201257-chr16:77223059..77224570,2	K562	blood:
30	chr16:77206067..77208430-chr16:77215088..77217473,2	MCF-7	breast:
31	chr16:76887924..76888465-chr16:77203271..77204023,2	MCF-7	breast:
32	chr16:75822932..75823933-chr16:77203258..77204234,7	MCF-7	breast:
33	chr1:200638562..200641266-chr16:77224293..77226737,2	MCF-7	breast:
34	chr16:75822791..75823761-chr16:77205366..77206287,6	MCF-7	breast:
35	chr16:76887878..76888800-chr16:77205307..77205910,4	MCF-7	breast:
36	chr16:77225300..77227094-chr16:77244120..77246217,2	MCF-7	breast:
37	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
38	chr16:77223627..77226316-chr16:77230976..77234622,5	MCF-7	breast:
39	chr16:75680135..75682966-chr16:77223241..77226200,3	MCF-7	breast:
40	chr16:77224130..77224935-chr22:41863949..41864740,2	Hela-S3	cervix:
41	chr11:66360307..66360987-chr16:77224555..77225280,2	Hela-S3	cervix:
42	chr16:75822777..75823699-chr16:77203448..77204260,4	K562	blood:
43	chr16:75588082..75590325-chr16:77223299..77225155,3	K562	blood:
44	chr16:77224632..77225508-chr5:43483543..43484113,2	Hela-S3	cervix:
45	chr16:75680522..75683233-chr16:77224728..77226496,3	MCF-7	breast:
46	chr16:77223287..77227235-chr16:77231893..77237199,5	MCF-7	breast:
47	chr16:77219105..77221826-chr16:77222885..77224694,2	MCF-7	breast:

No data

Variant related genes	Relation type
MON1B	TF binding region
MON1B	CpG island
ENSG00000103111	chromatin interactions
ENSG00000111011	chromatin interactions
ENSG00000159111	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000100410	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000198589	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000205078	chromatin interactions
ENSG00000141294	chromatin interactions
ENSG00000260088	chromatin interactions
ENSG00000118197	chromatin interactions
ENSG00000189079	chromatin interactions
ENSG00000226348	chromatin interactions
ENSG00000261717	chromatin interactions
ENSG00000173992	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000182791	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000205084	chromatin interactions
ENSG00000166848	chromatin interactions

Extended variants
information (count: 988 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:988 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182766994	chr16:77198613-77198614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573807177	chr16:77198620-77198621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572906423	chr16:77198622-77198623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559463411	chr16:77198623-77198624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148046492	chr16:77198701-77198702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140805085	chr16:77198704-77198705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188602850	chr16:77198728-77198729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542031438	chr16:77198729-77198730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35128579	chr16:77198730-77198731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71924823	chr16:77198731-77198732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145059552	chr16:77198739-77198740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574576752	chr16:77198766-77198767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535911214	chr16:77198767-77198768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549322896	chr16:77198800-77198801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193129778	chr16:77198820-77198821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138848327	chr16:77198842-77198843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559329804	chr16:77198845-77198846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555555817	chr16:77198846-77198847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141977025	chr16:77198849-77198850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7501311	chr16:77198866-77198867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185669206	chr16:77198872-77198873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543537837	chr16:77198881-77198882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563338348	chr16:77198889-77198890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs202101668	chr16:77198912-77198913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187735267	chr16:77198914-77198915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573668929	chr16:77198916-77198917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs386792337	chr16:77198921-77198922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115938349	chr16:77198922-77198923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539937180	chr16:77198950-77198951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191260933	chr16:77198959-77198960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573066233	chr16:77198971-77198972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369939949	chr16:77199007-77199008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545356150	chr16:77199154-77199155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184186898	chr16:77199199-77199200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530800194	chr16:77199236-77199237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541999753	chr16:77199241-77199242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543470644	chr16:77199263-77199264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563661612	chr16:77199271-77199272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs71134797	chr16:77199292-77199293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550169347	chr16:77199293-77199294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs398029965	chr16:77199306-77199307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529373661	chr16:77199319-77199320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549452072	chr16:77199336-77199337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188554213	chr16:77199352-77199353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146310728	chr16:77199364-77199365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532578000	chr16:77199382-77199383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551685569	chr16:77199391-77199392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs9934929	chr16:77199403-77199404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552553789	chr16:77199432-77199433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149650603	chr16:77199440-77199441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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	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
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	17363583	CNVD
Ovarian cancer	21720365	CNVD
Bipolar disorder	19114987	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77198600-77200200	Enhancers	Fetal Muscle Trunk	muscle
2	chr16:77199000-77199200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr16:77199200-77199800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr16:77199400-77200200	Enhancers	Fetal Muscle Leg	muscle
5	chr16:77200000-77200200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr16:77200200-77203200	Weak transcription	Fetal Muscle Leg	muscle
7	chr16:77203200-77203600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr16:77203200-77203800	Enhancers	Fetal Muscle Leg	muscle
9	chr16:77203600-77204800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr16:77203800-77204400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr16:77203800-77204400	Weak transcription	Fetal Muscle Leg	muscle
12	chr16:77204400-77205000	Enhancers	Fetal Muscle Leg	muscle
13	chr16:77204400-77206000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr16:77204600-77205000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr16:77204600-77205800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr16:77204800-77205400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr16:77205800-77206200	Flanking Active TSS	HUVEC	blood vessel
18	chr16:77206000-77206600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr16:77206000-77207600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr16:77206200-77207800	Enhancers	HUVEC	blood vessel
21	chr16:77206800-77207200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr16:77214000-77214800	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr16:77214200-77215000	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr16:77214200-77215200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr16:77214800-77215000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr16:77216800-77217200	Enhancers	NHEK	skin
27	chr16:77217200-77217600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr16:77217200-77217600	Flanking Active TSS	A549	lung
29	chr16:77217600-77218000	Enhancers	A549	lung
30	chr16:77222000-77223800	Enhancers	HepG2	liver
31	chr16:77222600-77224000	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr16:77223200-77223400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr16:77223200-77223400	Enhancers	Pancreas	Pancrea
34	chr16:77223200-77223400	Enhancers	Dnd41	blood
35	chr16:77223200-77223400	Active TSS	GM12878-XiMat	blood
36	chr16:77223200-77223600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr16:77223200-77223800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr16:77223200-77226200	Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr16:77223400-77223800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr16:77223400-77223800	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr16:77223400-77223800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr16:77223400-77223800	Flanking Active TSS	GM12878-XiMat	blood
43	chr16:77223400-77224000	Enhancers	Primary T cells fromperipheralblood	blood
44	chr16:77223400-77224000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr16:77223400-77224200	Flanking Active TSS	Dnd41	blood
46	chr16:77223400-77226600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr16:77223600-77223800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr16:77223600-77223800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr16:77223600-77223800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr16:77223600-77224000	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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