Variant report

Variant	nsv532200
Chromosome Location	chr5:119317901-120102513
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4625)
CpG islands
(count:2200)
Chromatin interactive
region (count:138)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4625 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:119848349-119848986	K562	blood:	n/a	n/a
2	ARID3A	chr5:119491596-119491838	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:119808789-119808848	K562	blood:	n/a	n/a
4	ARID3A	chr5:119741643-119741799	K562	blood:	n/a	n/a
5	ARID3A	chr5:119474632-119475168	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:119845695-119846337	K562	blood:	n/a	n/a
7	ARID3A	chr5:119853390-119853829	K562	blood:	n/a	n/a
8	ARID3A	chr5:119814969-119815009	K562	blood:	n/a	n/a
9	ATF1	chr5:119899838-119899993	K562	blood:	n/a	n/a
10	ATF1	chr5:119793643-119794138	K562	blood:	n/a	n/a
11	ATF1	chr5:119593725-119594109	K562	blood:	n/a	n/a
12	ATF1	chr5:119474813-119475088	K562	blood:	n/a	n/a
13	ATF1	chr5:119853689-119853917	K562	blood:	n/a	n/a
14	ATF1	chr5:119488288-119488483	K562	blood:	n/a	n/a
15	ATF1	chr5:119694688-119694905	K562	blood:	n/a	n/a
16	ATF1	chr5:119565022-119565105	K562	blood:	n/a	n/a
17	ATF1	chr5:119393482-119393828	K562	blood:	n/a	n/a
18	ATF1	chr5:119640444-119640591	K562	blood:	n/a	n/a
19	ATF1	chr5:119318458-119318658	K562	blood:	n/a	n/a
20	ATF1	chr5:119607567-119607671	K562	blood:	n/a	n/a
21	ATF1	chr5:119848381-119848909	K562	blood:	n/a	n/a
22	ATF2	chr5:120033417-120033942	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr5:120042574-120042977	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr5:120031373-120031760	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr5:120030827-120031258	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr5:120042500-120043085	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr5:119847523-119848070	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr5:120032153-120033315	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr5:119802291-119802654	GM12878	blood:	n/a	n/a
30	ATF2	chr5:119793456-119794141	GM12878	blood:	n/a	n/a
31	ATF2	chr5:119793413-119794075	GM12878	blood:	n/a	n/a
32	ATF3	chr5:119848349-119848681	K562	blood:	n/a	n/a
33	ATF3	chr5:119799801-119800020	K562	blood:	n/a	n/a
34	ATF3	chr5:119793562-119793757	K562	blood:	n/a	n/a
35	ATF3	chr5:119793581-119793842	K562	blood:	n/a	n/a
36	ATF3	chr5:119793531-119793905	GM12878	blood:	n/a	n/a
37	ATF3	chr5:119793575-119793776	GM12878	blood:	n/a	n/a
38	BACH1	chr5:119697785-119697924	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr5:119370023-119370074	K562	blood:	n/a	n/a
40	BACH1	chr5:120023318-120023332	K562	blood:	n/a	n/a
41	BACH1	chr5:119318639-119318660	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr5:119959300-119959328	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr5:120026709-120027291	H1-hESC	embryonic stem cell:	n/a	n/a
44	BATF	chr5:119793535-119793841	GM12878	blood:	n/a	n/a
45	BATF	chr5:119802379-119802613	GM12878	blood:	n/a	n/a
46	BATF	chr5:119714603-119715029	GM12878	blood:	n/a	n/a
47	BATF	chr5:119793497-119794263	GM12878	blood:	n/a	n/a
48	BATF	chr5:119714670-119714992	GM12878	blood:	n/a	n/a
49	BCL11A	chr5:119793538-119794246	GM12878	blood:	n/a	n/a
50	BCL11A	chr5:119714620-119715075	GM12878	blood:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120069936-120069986	RPTEC	kidney:	n/a
2	chr5:119942454-119942504	NB4	blood:	n/a
3	chr5:119799832-119799882	LNCaP	prostate:	n/a
4	chr5:119801431-119801481	HepG2	liver:	n/a
5	chr5:120069936-120069986	RPTEC	kidney:	n/a
6	chr5:119942454-119942504	NB4	blood:	n/a
7	chr5:119799832-119799882	LNCaP	prostate:	n/a
8	chr5:119801431-119801481	HepG2	liver:	n/a
9	chr5:120038247-120038297	HIPEpiC	eye:	n/a
10	chr5:119799531-119799581	HEK293	kidney:	embryo
11	chr5:119799220-119799270	SK-N-SH_RA	brain:	n/a
12	chr5:119799384-119799434	GM19239	blood:	n/a
13	chr5:120040283-120040333	K562	blood:	n/a
14	chr5:119801193-119801243	HAEpiC	amniotic membrane:	n/a
15	chr5:119801431-119801481	ovcar-3	ovarian:	n/a
16	chr5:119942454-119942504	HCF	heart:	n/a
17	chr5:119495957-119496007	SAEC	small airway:	n/a
18	chr5:120018164-120018214	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:119488431-119488481	SAEC	small airway:	n/a
20	chr5:119952679-119952729	MCF-7	breast:	n/a
21	chr5:119952679-119952729	PrEC	prostate:	n/a
22	chr5:120069936-120069986	NH-A	brain:	n/a
23	chr5:119801193-119801243	ECC-1	luminal epithelium:	n/a
24	chr5:119495957-119496007	HEEpiC	esophagus:	n/a
25	chr5:119801431-119801481	A549	lung:	n/a
26	chr5:119800687-119800737	Jurkat	blood:	n/a
27	chr5:119782696-119782746	GM19239	blood:	n/a
28	chr5:119864497-119864547	PrEC	prostate:	n/a
29	chr5:119517834-119517884	BE2_C	brain:	n/a
30	chr5:119800234-119800284	SAEC	small airway:	n/a
31	chr5:120038247-120038297	SAEC	small airway:	n/a
32	chr5:119846291-119846341	NH-A	brain:	n/a
33	chr5:119952679-119952729	GM12892	blood:	n/a
34	chr5:119951527-119951577	ProgFib	skin:	n/a
35	chr5:119799864-119799914	HEK293	kidney:	embryo
36	chr5:120097654-120097704	AG09309	skin:	n/a
37	chr5:119799220-119799270	RPTEC	kidney:	n/a
38	chr5:119951527-119951577	AG09319	gingival:	n/a
39	chr5:120018164-120018214	A549	lung:	n/a
40	chr5:119801193-119801243	GM19239	blood:	n/a
41	chr5:119799822-119799872	GM06990	blood:	n/a
42	chr5:119952679-119952729	NT2-D1	testis:	n/a
43	chr5:119801643-119801693	AG10803	skin:	n/a
44	chr5:119799384-119799434	MCF-7	breast:	n/a
45	chr5:119952679-119952729	AG04449	skin:	fetal
46	chr5:119799862-119799912	NB4	blood:	n/a
47	chr5:119495957-119496007	NB4	blood:	n/a
48	chr5:119802022-119802072	AG09319	gingival:	n/a
49	chr5:119942454-119942504	ECC-1	luminal epithelium:	n/a
50	chr5:120026632-120026682	GM12878	blood:	n/a

(count:138 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:120040953..120043952-chr5:120045648..120047608,2	K562	blood:
2	chr5:119390926..119393461-chr5:119405366..119407503,2	K562	blood:
3	chr5:119886756..119889709-chr5:119891670..119893322,2	K562	blood:
4	chr5:119719801..119721845-chr5:119723016..119725406,2	K562	blood:
5	chr5:119991257..119992549-chr5:121285272..121286241,6	MCF-7	breast:
6	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
7	chr5:120082635..120085459-chr5:120095219..120098019,2	K562	blood:
8	chr5:119991420..119991957-chr5:121285300..121286207,2	MCF-7	breast:
9	chr5:119814891..119816438-chr5:119818822..119820625,2	K562	blood:
10	chr5:119792597..119795401-chr5:119799043..119801706,2	K562	blood:
11	chr5:119322458..119322958-chr8:143315608..143316280,2	MCF-7	breast:
12	chr5:119680201..119681861-chr5:119689913..119692510,2	K562	blood:
13	chr5:119490690..119493114-chr7:5464157..5466979,2	MCF-7	breast:
14	chr5:119688806..119691602-chr5:119693680..119696391,2	K562	blood:
15	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
16	chr5:119784118..119786225-chr5:119788090..119789969,2	K562	blood:
17	chr5:119851956..119854339-chr5:119862015..119863785,2	K562	blood:
18	chr5:119644924..119647255-chr5:119650755..119652269,2	MCF-7	breast:
19	chr5:119522399..119524409-chr5:119526483..119528951,2	K562	blood:
20	chr5:119769254..119771036-chr5:119773578..119776402,2	K562	blood:
21	chr14:81685904..81686476-chr5:119526721..119527705,2	NB4	blood:
22	chr5:119611234..119613467-chr5:119620898..119622860,2	K562	blood:
23	chr5:119769254..119771036-chr5:119773578..119776402,2	K562	blood:
24	chr5:119803768..119806715-chr5:119850808..119853246,2	K562	blood:
25	chr3:99997776..99998276-chr5:119383981..119384507,2	MCF-7	breast:
26	chr5:119835822..119838149-chr5:119840873..119842800,2	K562	blood:
27	chr5:119801561..119803830-chr5:119805628..119808715,3	K562	blood:
28	chr5:119847102..119848643-chr5:119877942..119880653,2	K562	blood:
29	chr5:119806492..119808449-chr5:119834650..119836281,2	K562	blood:
30	chr5:119605903..119607846-chr5:119609534..119611047,2	K562	blood:
31	chr5:119851956..119853481-chr5:119862285..119864209,2	K562	blood:
32	chr5:119661450..119663428-chr5:119666004..119667797,2	K562	blood:
33	chr5:119688806..119691602-chr5:119693680..119696391,2	K562	blood:
34	chr5:119801016..119803100-chr5:119851238..119853983,3	K562	blood:
35	chr5:119719801..119721845-chr5:119723016..119725406,2	K562	blood:
36	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
37	chr5:120076937..120079853-chr5:120080038..120082536,3	K562	blood:
38	chr5:119889111..119891337-chr5:119901156..119903856,2	K562	blood:
39	chr5:119803768..119806455-chr5:119850808..119853040,2	K562	blood:
40	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
41	chr5:119859163..119862505-chr5:119863189..119865594,3	K562	blood:
42	chr5:119806492..119808449-chr5:119834650..119836281,2	K562	blood:
43	chr5:119858416..119860878-chr5:119871767..119873808,2	K562	blood:
44	chr5:120072445..120075135-chr5:120093078..120094683,2	K562	blood:
45	chr5:119852641..119855403-chr5:119858663..119861465,3	K562	blood:
46	chr5:119522399..119524409-chr5:119526483..119528951,2	K562	blood:
47	chr5:120009986..120011754-chr5:120014103..120015876,2	K562	blood:
48	chr5:119398548..119400773-chr5:119411952..119413721,2	K562	blood:
49	chr5:119425445..119427707-chr5:119431108..119433766,2	MCF-7	breast:
50	chr5:119775909..119777540-chr5:119783720..119785397,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-5	chr5:119740450-119740532	ENSG00000261036.1
2	lnc-FAM170A-2	chr5:119328116-119328211	l_3004_chr5:119198853-119375297_testes
3	lnc-DTWD2-5	chr5:119681602-119682035	ENSG00000261036.1
4	lnc-FAM170A-2	chr5:119341293-119341390	l_3004_chr5:119198853-119375297_testes
5	lnc-LOX-9	chr5:119993772-119994066	NONHSAT103445
6	lnc-DTWD2-4	chr5:119668951-119669197	XLOC_004969
7	lnc-FAM170A-2	chr5:119375212-119375297	l_3004_chr5:119198853-119375297_testes
8	lnc-DTWD2-4	chr5:119581143-119581328	XLOC_004969

No data

Variant related genes	Relation type
RNU6-718P	TF binding region
PRR16	TF binding region
ENSG00000270741	TF binding region
ENSG00000251293	TF binding region
RNU4-69P	TF binding region
ENSG00000261036	TF binding region
RNU6-718P	CpG island
PRR16	CpG island
ENSG00000270741	CpG island
ENSG00000251293	CpG island
RNU4-69P	CpG island
ENSG00000261036	CpG island
ENSG00000184838	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000222609	chromatin interactions
ENSG00000182095	chromatin interactions

Extended variants
information (count: 25162 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:25162 , 50 per page) page: 1 2 3 4 5 6 7 ... 504

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114057578	chr5:119317915-119317916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7718340	chr5:119317946-119317947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544045694	chr5:119317949-119317950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186679472	chr5:119317974-119317975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116188682	chr5:119318087-119318088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73256701	chr5:119318104-119318105	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs375428110	chr5:119318118-119318119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191432106	chr5:119318202-119318203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139491638	chr5:119318212-119318213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149705791	chr5:119318227-119318228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572114244	chr5:119318239-119318240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12513439	chr5:119318268-119318269	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs560845554	chr5:119318303-119318304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529964292	chr5:119318338-119318339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145343257	chr5:119318340-119318341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12513497	chr5:119318359-119318360	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs532187566	chr5:119318371-119318372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140147601	chr5:119318404-119318405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182186638	chr5:119318405-119318406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs56063154	chr5:119318413-119318414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112339692	chr5:119318421-119318422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548237742	chr5:119318468-119318469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115187502	chr5:119318478-119318479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536963035	chr5:119318479-119318480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541676209	chr5:119318518-119318519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556687083	chr5:119318525-119318526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534382581	chr5:119318537-119318538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576562293	chr5:119318561-119318562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115055258	chr5:119318566-119318567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188881479	chr5:119318601-119318602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572251619	chr5:119318619-119318620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541005683	chr5:119318654-119318655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77342248	chr5:119318693-119318694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574355625	chr5:119318704-119318705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143879056	chr5:119318732-119318733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553608552	chr5:119318742-119318743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377172779	chr5:119318746-119318747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13154208	chr5:119318747-119318748	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546028460	chr5:119318823-119318824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559472714	chr5:119318828-119318829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574842194	chr5:119318863-119318864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371449906	chr5:119318949-119318950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528232687	chr5:119318959-119318960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs61178406	chr5:119319012-119319013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548177028	chr5:119319052-119319053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568082757	chr5:119319086-119319087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193239784	chr5:119319136-119319137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146869966	chr5:119319157-119319158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140726553	chr5:119319165-119319166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185240655	chr5:119319214-119319215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:3410 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119317600-119320000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:119330400-119330800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:119330400-119330800	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr5:119330800-119332000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:119331400-119332200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:119331600-119332200	Enhancers	Psoas Muscle	Psoas
7	chr5:119332000-119332200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:119337200-119337800	Enhancers	HSMM	muscle
9	chr5:119340800-119341200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr5:119341600-119341800	Enhancers	Brain Germinal Matrix	brain
11	chr5:119341800-119342800	Weak transcription	Brain Germinal Matrix	brain
12	chr5:119342800-119343400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr5:119342800-119344600	Enhancers	Brain Germinal Matrix	brain
14	chr5:119342800-119346000	Enhancers	Hela-S3	cervix
15	chr5:119343000-119344400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:119343200-119343600	Enhancers	Fetal Brain Male	brain
17	chr5:119343200-119344000	Enhancers	Colon Smooth Muscle	Colon
18	chr5:119343200-119344400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:119344400-119345600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:119344400-119348400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr5:119345000-119345200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr5:119345600-119346000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr5:119346000-119352400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:119348000-119348800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:119348400-119348800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr5:119350400-119350600	ZNF genes & repeats	HSMMtube	muscle
27	chr5:119350600-119352800	Weak transcription	HSMMtube	muscle
28	chr5:119351800-119352600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:119352400-119353200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr5:119352600-119353600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:119352800-119353600	Enhancers	Hela-S3	cervix
32	chr5:119352800-119353800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:119352800-119353800	Enhancers	HSMMtube	muscle
34	chr5:119353000-119353400	Enhancers	HMEC	breast
35	chr5:119353000-119353800	Enhancers	NHDF-Ad	bronchial
36	chr5:119353200-119357200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:119353400-119353800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr5:119358800-119359200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr5:119365800-119366800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:119366200-119366600	Enhancers	Fetal Stomach	stomach
41	chr5:119372400-119374000	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr5:119372600-119373000	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr5:119372600-119373800	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr5:119373000-119373600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr5:119373600-119374000	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr5:119373800-119375200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr5:119374000-119375200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr5:119374000-119375400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr5:119375200-119376000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr5:119375200-119376000	Enhancers	Monocytes-CD14+_RO01746	blood

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