Variant report

Variant	nsv181
Chromosome Location	chr19:52113123-52162533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:914)
CpG islands
(count:795)
Chromatin interactive
region (count:42)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52140651-52140961	K562	blood:	n/a	n/a
2	ARID3A	chr19:52160074-52160493	K562	blood:	n/a	n/a
3	ATF1	chr19:52154746-52155090	K562	blood:	n/a	n/a
4	ATF1	chr19:52124551-52124727	K562	blood:	n/a	n/a
5	ATF2	chr19:52154376-52154835	GM12878	blood:	n/a	n/a
6	ATF2	chr19:52124388-52124859	GM12878	blood:	n/a	n/a
7	ATF2	chr19:52113850-52114201	GM12878	blood:	n/a	n/a
8	BATF	chr19:52124396-52124758	GM12878	blood:	n/a	n/a
9	BATF	chr19:52113844-52114148	GM12878	blood:	n/a	n/a
10	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
11	BATF	chr19:52113804-52114200	GM12878	blood:	n/a	n/a
12	BATF	chr19:52118807-52119121	GM12878	blood:	n/a	n/a
13	BATF	chr19:52133523-52133840	GM12878	blood:	n/a	n/a
14	BCL11A	chr19:52124451-52124734	GM12878	blood:	n/a	n/a
15	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
16	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
17	BCL11A	chr19:52124445-52124855	GM12878	blood:	n/a	n/a
18	BCL3	chr19:52131741-52132214	GM12878	blood:	n/a	n/a
19	BCL3	chr19:52131621-52132296	GM12878	blood:	n/a	n/a
20	BCLAF1	chr19:52113796-52114240	GM12878	blood:	n/a	n/a
21	BCLAF1	chr19:52124371-52124835	GM12878	blood:	n/a	n/a
22	BCLAF1	chr19:52124469-52124839	GM12878	blood:	n/a	n/a
23	BHLHE40	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
24	BHLHE40	chr19:52133577-52133941	GM12878	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
25	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
26	BHLHE40	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
27	BHLHE40	chr19:52154406-52154749	GM12878	blood:	n/a	n/a
28	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
29	BHLHE40	chr19:52160071-52160612	K562	blood:	n/a	n/a
30	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
31	CBX3	chr19:52160019-52160455	K562	blood:	n/a	n/a
32	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
33	CBX3	chr19:52159942-52160552	K562	blood:	n/a	n/a
34	CBX3	chr19:52157930-52158454	K562	blood:	n/a	n/a
35	CBX3	chr19:52157924-52158374	K562	blood:	n/a	n/a
36	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
37	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
38	CEBPB	chr19:52135506-52135630	K562	blood:	n/a	n/a
39	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
40	CEBPB	chr19:52119481-52119697	A549	lung:	n/a	chr19:52119654-52119665 chr19:52119563-52119576
41	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
42	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
43	CEBPB	chr19:52119469-52119692	HepG2	liver:	n/a	chr19:52119654-52119665 chr19:52119563-52119576
44	CEBPB	chr19:52131571-52131646	K562	blood:	n/a	n/a
45	CEBPB	chr19:52119395-52119727	MCF-7	breast:	n/a	chr19:52119654-52119665 chr19:52119563-52119576
46	CEBPB	chr19:52160197-52160526	K562	blood:	n/a	n/a
47	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
48	CTCF	chr19:52140750-52140910	LNCaP	prostate:	n/a	n/a
49	CTCF	chr19:52160340-52160490	HCM	heart:	n/a	chr19:52160373-52160394 chr19:52160384-52160393 chr19:52160378-52160396 chr19:52160380-52160393
50	CTCF	chr19:52140550-52141144	HCT-116	colon:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52146598-52146648	Caco-2	colon:	n/a
2	chr19:52150634-52150684	SK-N-SH	brain:	n/a
3	chr19:52146598-52146648	Caco-2	colon:	n/a
4	chr19:52150634-52150684	SK-N-SH	brain:	n/a
5	chr19:52114809-52114859	AG04450	lung:	fetal
6	chr19:52134296-52134346	GM19239	blood:	n/a
7	chr19:52134393-52134443	GM12878	blood:	n/a
8	chr19:52134296-52134346	Hela-S3	cervix:	n/a
9	chr19:52134393-52134443	HUVEC	blood vessel:	n/a
10	chr19:52134289-52134339	GM19239	blood:	n/a
11	chr19:52133837-52133887	HCM	heart:	n/a
12	chr19:52134296-52134346	HepG2	liver:	n/a
13	chr19:52131310-52131360	NH-A	brain:	n/a
14	chr19:52133837-52133887	ProgFib	skin:	n/a
15	chr19:52146598-52146648	HEK293	kidney:	embryo
16	chr19:52131310-52131360	AG09319	gingival:	n/a
17	chr19:52150233-52150283	HMEC	breast:	n/a
18	chr19:52134296-52134346	SK-N-SH	brain:	n/a
19	chr19:52114809-52114859	HPAEpiC	pulmonary alveolar:	n/a
20	chr19:52131310-52131360	AG04449	skin:	fetal
21	chr19:52114809-52114859	IMR90	lung:	fetal
22	chr19:52146598-52146648	SK-N-SH	brain:	n/a
23	chr19:52134296-52134346	NHDF-neo	bronchial:	n/a
24	chr19:52146598-52146648	AG09319	gingival:	n/a
25	chr19:52150634-52150684	ovcar-3	ovarian:	n/a
26	chr19:52131310-52131360	HCM	heart:	n/a
27	chr19:52150230-52150280	NHBE	bronchial:	n/a
28	chr19:52150547-52150597	SK-N-MC	brain:	n/a
29	chr19:52150547-52150597	HUVEC	blood vessel:	n/a
30	chr19:52140097-52140147	Caco-2	colon:	n/a
31	chr19:52146598-52146648	PrEC	prostate:	n/a
32	chr19:52134393-52134443	NT2-D1	testis:	n/a
33	chr19:52134393-52134443	SAEC	small airway:	n/a
34	chr19:52114809-52114859	HL-60	blood:	n/a
35	chr19:52133837-52133887	ovcar-3	ovarian:	n/a
36	chr19:52134289-52134339	HCF	heart:	n/a
37	chr19:52150233-52150283	HAEpiC	amniotic membrane:	n/a
38	chr19:52134289-52134339	HepG2	liver:	n/a
39	chr19:52134296-52134346	PFSK-1	brain:	n/a
40	chr19:52134393-52134443	HCF	heart:	n/a
41	chr19:52146598-52146648	NT2-D1	testis:	n/a
42	chr19:52148354-52148404	HUVEC	blood vessel:	n/a
43	chr19:52133837-52133887	GM12878	blood:	n/a
44	chr19:52150230-52150280	AG04449	skin:	fetal
45	chr19:52134393-52134443	AG09309	skin:	n/a
46	chr19:52134393-52134443	SKMC	muscle:	n/a
47	chr19:52114809-52114859	HCM	heart:	n/a
48	chr19:52148354-52148404	GM06990	blood:	n/a
49	chr19:52150634-52150684	NH-A	brain:	n/a
50	chr19:52150634-52150684	NB4	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
2	chr19:52110618..52112664-chr19:52114237..52116564,2	K562	blood:
3	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:
4	chr19:52113611..52116176-chr19:52178728..52181472,2	MCF-7	breast:
5	chr19:52107187..52109556-chr19:52121301..52123809,2	K562	blood:
6	chr19:51925281..51925822-chr19:52159922..52160574,2	MCF-7	breast:
7	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
8	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
9	chr19:51975913..51977254-chr19:52159906..52161263,12	MCF-7	breast:
10	chr19:51874861..51877749-chr19:52158879..52160406,2	K562	blood:
11	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
12	chr19:51965493..51967976-chr19:52153295..52156025,2	K562	blood:
13	chr19:51975931..51976838-chr19:52160089..52160663,2	MCF-7	breast:
14	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
15	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:
16	chr19:52050819..52052546-chr19:52117300..52119490,2	K562	blood:
17	chr19:52160319..52160911-chr19:52311474..52312517,3	K562	blood:
18	chr19:52110556..52111829-chr19:52157738..52158676,7	MCF-7	breast:
19	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
20	chr19:52110839..52111869-chr19:52159924..52160844,8	MCF-7	breast:
21	chr19:52014761..52015333-chr19:52159948..52160615,2	MCF-7	breast:
22	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:
23	chr19:52117245..52119688-chr19:52127612..52129163,2	K562	blood:
24	chr19:52159931..52161750-chr19:52173076..52176072,2	K562	blood:
25	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
26	chr19:52117245..52119688-chr19:52127612..52129163,2	K562	blood:
27	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
28	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
29	chr19:52118220..52120065-chr19:52121660..52123490,2	K562	blood:
30	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
31	chr19:51924885..51925819-chr19:52159862..52160853,7	K562	blood:
32	chr19:52107630..52109611-chr19:52113682..52115927,2	K562	blood:
33	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
34	chr19:52118220..52120065-chr19:52121660..52123490,2	K562	blood:
35	chr19:51620285..51621823-chr19:52126371..52128453,2	K562	blood:
36	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
37	chr19:52160347..52160857-chr19:52281258..52281779,2	K562	blood:
38	chr19:52096393..52097985-chr19:52116487..52118530,2	MCF-7	breast:
39	chr19:51975890..51976812-chr19:52159933..52160756,4	K562	blood:
40	chr19:51873847..51875580-chr19:52152831..52155624,2	K562	blood:
41	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:
42	chr19:52110880..52111497-chr19:52159833..52160812,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIGLEC14-1	chr19:52133354-52133469	ENSG00000258669.1
2	lnc-ZNF175-4	chr19:52124389-52124954	NONHSAT067457
3	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1
4	lnc-ZNF175-5	chr19:52152115-52152863	NONHSAT067458
5	lnc-SIGLEC14-1	chr19:52133552-52133919	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC14	TF binding region
RPL9P33	TF binding region
ENSG00000268500	TF binding region
RPL7P51	TF binding region
SIGLEC5	TF binding region
SIGLEC14	CpG island
RPL9P33	CpG island
ENSG00000268500	CpG island
RPL7P51	CpG island
SIGLEC5	CpG island
ENSG00000167765	chromatin interactions
ENSG00000105366	chromatin interactions
ENSG00000269388	chromatin interactions
ENSG00000244071	chromatin interactions
ENSG00000213822	chromatin interactions
ENSG00000105374	chromatin interactions
ENSG00000105501	chromatin interactions

Extended variants
information (count: 2018 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139081719	chr19:52113138-52113139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs202167942	chr19:52113149-52113150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184134341	chr19:52113177-52113178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188459391	chr19:52113208-52113209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80185767	chr19:52113209-52113210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571931028	chr19:52113224-52113225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191349566	chr19:52113227-52113228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564414525	chr19:52113236-52113237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117319482	chr19:52113248-52113249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550997427	chr19:52113249-52113250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562816458	chr19:52113251-52113252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142026838	chr19:52113273-52113274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548713495	chr19:52113275-52113276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146322290	chr19:52113318-52113319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs8100771	chr19:52113339-52113340	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs576639845	chr19:52113408-52113409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543625377	chr19:52113429-52113430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561958683	chr19:52113450-52113451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4802828	chr19:52113538-52113539	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs571166900	chr19:52113539-52113540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537440605	chr19:52113576-52113577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556152783	chr19:52113585-52113586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568048543	chr19:52113657-52113658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115306699	chr19:52113672-52113673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138237642	chr19:52113761-52113762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112888107	chr19:52113763-52113764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571867252	chr19:52113768-52113769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550169726	chr19:52113776-52113777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142721668	chr19:52113783-52113784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557762479	chr19:52113857-52113858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576310553	chr19:52113882-52113883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559043304	chr19:52114004-52114005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544262954	chr19:52114113-52114114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562864901	chr19:52114131-52114132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530141034	chr19:52114133-52114134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542299007	chr19:52114145-52114146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560580403	chr19:52114157-52114158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534804979	chr19:52114169-52114170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554488622	chr19:52114189-52114190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78032490	chr19:52114250-52114251	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552783974	chr19:52114297-52114298	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116894305	chr19:52114353-52114354	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569388673	chr19:52114357-52114358	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532066138	chr19:52114396-52114397	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536792775	chr19:52114406-52114407	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114134570	chr19:52114421-52114422	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568001393	chr19:52114493-52114494	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535089133	chr19:52114503-52114504	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74387205	chr19:52114541-52114542	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144412584	chr19:52114646-52114647	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52109600-52114200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr19:52110600-52114200	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr19:52111400-52114200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr19:52111600-52115800	Weak transcription	Spleen	Spleen
5	chr19:52111800-52115000	Weak transcription	Primary B cells from cord blood	blood
6	chr19:52112200-52113400	Weak transcription	GM12878-XiMat	blood
7	chr19:52112200-52115000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr19:52112200-52115000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr19:52112400-52113800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr19:52113400-52113800	Enhancers	GM12878-XiMat	blood
11	chr19:52113800-52114200	Enhancers	Primary B cells from peripheral blood	blood
12	chr19:52113800-52114600	Weak transcription	GM12878-XiMat	blood
13	chr19:52114200-52114600	Weak transcription	Primary B cells from peripheral blood	blood
14	chr19:52114200-52118800	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr19:52114200-52119000	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr19:52114200-52122200	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr19:52114600-52114800	Enhancers	GM12878-XiMat	blood
18	chr19:52114600-52116200	Strong transcription	Primary B cells from peripheral blood	blood
19	chr19:52115000-52115800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr19:52115000-52116200	Strong transcription	Primary B cells from cord blood	blood
21	chr19:52115000-52116600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
22	chr19:52115800-52116200	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:52115800-52116600	ZNF genes & repeats	Spleen	Spleen
24	chr19:52116200-52116600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
25	chr19:52116200-52117600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr19:52116200-52123400	Weak transcription	Primary B cells from cord blood	blood
27	chr19:52116600-52117000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr19:52116600-52118800	Strong transcription	Primary B cells from peripheral blood	blood
29	chr19:52116600-52130200	Weak transcription	Spleen	Spleen
30	chr19:52117000-52117200	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr19:52117000-52117400	Enhancers	GM12878-XiMat	blood
32	chr19:52117200-52117600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr19:52117600-52117800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr19:52117600-52118400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr19:52117800-52123000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr19:52118400-52119400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr19:52118600-52119000	Bivalent Enhancer	GM12878-XiMat	blood
38	chr19:52118600-52120600	Enhancers	Placenta	Placenta
39	chr19:52118800-52119200	Genic enhancers	Primary B cells from peripheral blood	blood
40	chr19:52118800-52119600	Genic enhancers	Primary monocytes fromperipheralblood	blood
41	chr19:52118800-52121400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr19:52119000-52119600	Enhancers	GM12878-XiMat	blood
43	chr19:52119000-52119600	Genic enhancers	Monocytes-CD14+_RO01746	blood
44	chr19:52119200-52121600	Strong transcription	Primary B cells from peripheral blood	blood
45	chr19:52119400-52128200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr19:52119600-52122800	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr19:52119600-52123000	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr19:52119600-52123600	Weak transcription	GM12878-XiMat	blood
49	chr19:52120600-52121600	Weak transcription	Placenta	Placenta
50	chr19:52121600-52121800	Enhancers	Placenta	Placenta

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