Variant report

Variant	esv3438795
Chromosome Location	chr19:52132440-52151238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:350)
CpG islands
(count:672)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:350 , 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	ARID3A	chr19:52140651-52140961	K562	blood:	n/a	n/a
2	BATF	chr19:52133523-52133840	GM12878	blood:	n/a	n/a
3	BATF	chr19:52149947-52150214	GM12878	blood:	n/a	n/a
4	BCL11A	chr19:52149937-52150305	GM12878	blood:	n/a	n/a
5	BCL11A	chr19:52133513-52133816	GM12878	blood:	n/a	n/a
6	BHLHE40	chr19:52147812-52147863	K562	blood:	n/a	n/a
7	BHLHE40	chr19:52133577-52133941	GM12878	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
8	BHLHE40	chr19:52133583-52133837	K562	blood:	n/a	chr19:52133745-52133754 chr19:52133745-52133754
9	BHLHE40	chr19:52150049-52150408	GM12878	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
10	BHLHE40	chr19:52150088-52150405	K562	blood:	n/a	chr19:52150169-52150178 chr19:52150169-52150178
11	CBX3	chr19:52140579-52140964	K562	blood:	n/a	n/a
12	CBX3	chr19:52140595-52141003	K562	blood:	n/a	n/a
13	CEBPB	chr19:52144942-52145259	A549	lung:	n/a	chr19:52145111-52145122
14	CEBPB	chr19:52135506-52135630	K562	blood:	n/a	n/a
15	CEBPB	chr19:52135381-52135805	MCF-7	breast:	n/a	n/a
16	CEBPB	chr19:52144983-52145193	IMR90	lung:	n/a	chr19:52145111-52145122
17	CEBPB	chr19:52145000-52145199	K562	blood:	n/a	chr19:52145111-52145122
18	CEBPB	chr19:52144962-52145257	HepG2	liver:	n/a	chr19:52145111-52145122
19	CEBPB	chr19:52135414-52135743	MCF-7	breast:	n/a	n/a
20	CTCF	chr19:52140740-52140890	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr19:52140740-52140890	GM12874	blood:	n/a	n/a
22	CTCF	chr19:52140680-52140830	MCF-7	breast:	n/a	n/a
23	CTCF	chr19:52140760-52140910	GM12864	blood:	n/a	n/a
24	CTCF	chr19:52140740-52140890	HCFaa	heart:	n/a	n/a
25	CTCF	chr19:52140740-52140890	GM12864	blood:	n/a	n/a
26	CTCF	chr19:52140741-52140925	GM10266	blood:	n/a	n/a
27	CTCF	chr19:52140740-52140890	GM12869	blood:	n/a	n/a
28	CTCF	chr19:52149824-52149845	GM19239	blood:	n/a	n/a
29	CTCF	chr19:52140729-52140884	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr19:52140613-52141009	K562	blood:	n/a	n/a
31	CTCF	chr19:52140740-52140890	NB4	blood:	n/a	n/a
32	CTCF	chr19:52140797-52140906	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:52150420-52150570	GM12872	blood:	n/a	n/a
34	CTCF	chr19:52140800-52140950	GM12872	blood:	n/a	n/a
35	CTCF	chr19:52140760-52140910	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr19:52140720-52140870	AG04449	skin:	n/a	n/a
37	CTCF	chr19:52140740-52140890	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr19:52140780-52140930	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr19:52140720-52140870	NHEK	skin:	n/a	n/a
40	CTCF	chr19:52140760-52140910	GM12872	blood:	n/a	n/a
41	CTCF	chr19:52140780-52140930	GM12866	blood:	n/a	n/a
42	CTCF	chr19:52140720-52140870	HPF	lung:	n/a	n/a
43	CTCF	chr19:52140723-52140918	A549	lung:	n/a	n/a
44	CTCF	chr19:52140780-52140930	BE2_C	brain:	n/a	n/a
45	CTCF	chr19:52140780-52140930	GM12868	blood:	n/a	n/a
46	CTCF	chr19:52140765-52140908	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr19:52140740-52140890	GM06990	blood:	n/a	n/a
48	CTCF	chr19:52140828-52140930	A549	lung:	n/a	n/a
49	CTCF	chr19:52140760-52140910	HMEC	breast:	n/a	n/a
50	CTCF	chr19:52141072-52141194	K562	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52146598-52146648	HepG2	liver:	n/a
2	chr19:52146598-52146648	HepG2	liver:	n/a
3	chr19:52148354-52148404	SK-N-SH_RA	brain:	n/a
4	chr19:52140097-52140147	Jurkat	blood:	n/a
5	chr19:52150547-52150597	PrEC	prostate:	n/a
6	chr19:52134296-52134346	HRCEpiC	kidney:	n/a
7	chr19:52146598-52146648	HAEpiC	amniotic membrane:	n/a
8	chr19:52134393-52134443	AoSMC	blood vessel:	n/a
9	chr19:52133837-52133887	PANC-1	pancreas:	n/a
10	chr19:52150230-52150280	GM06990	blood:	n/a
11	chr19:52150634-52150684	IMR90	lung:	fetal
12	chr19:52150547-52150597	AG04450	lung:	fetal
13	chr19:52140097-52140147	NB4	blood:	n/a
14	chr19:52134393-52134443	ovcar-3	ovarian:	n/a
15	chr19:52133837-52133887	AoSMC	blood vessel:	n/a
16	chr19:52150233-52150283	BJ	skin:	n/a
17	chr19:52148354-52148404	HUVEC	blood vessel:	n/a
18	chr19:52150547-52150597	Hepatocyte	liver:	n/a
19	chr19:52134296-52134346	HAEpiC	amniotic membrane:	n/a
20	chr19:52134296-52134346	AG04450	lung:	fetal
21	chr19:52150233-52150283	NB4	blood:	n/a
22	chr19:52146598-52146648	RPTEC	kidney:	n/a
23	chr19:52150634-52150684	HCPEpiC	choroid plexus:	n/a
24	chr19:52134289-52134339	NHBE	bronchial:	n/a
25	chr19:52133837-52133887	MCF10A-Er-Src	breast:	n/a
26	chr19:52146598-52146648	NHBE	bronchial:	n/a
27	chr19:52134289-52134339	HCT-116	colon:	n/a
28	chr19:52134393-52134443	HUVEC	blood vessel:	n/a
29	chr19:52134393-52134443	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:52150634-52150684	A549	lung:	n/a
31	chr19:52148354-52148404	SK-N-SH	brain:	n/a
32	chr19:52134393-52134443	HIPEpiC	eye:	n/a
33	chr19:52146598-52146648	Jurkat	blood:	n/a
34	chr19:52146598-52146648	HCT-116	colon:	n/a
35	chr19:52150547-52150597	GM12892	blood:	n/a
36	chr19:52146598-52146648	ProgFib	skin:	n/a
37	chr19:52140097-52140147	IMR90	lung:	fetal
38	chr19:52133837-52133887	HUVEC	blood vessel:	n/a
39	chr19:52150230-52150280	SK-N-SH	brain:	n/a
40	chr19:52150547-52150597	PANC-1	pancreas:	n/a
41	chr19:52150230-52150280	H1-hESC	embryonic stem cell:	embryo
42	chr19:52140097-52140147	NHBE	bronchial:	n/a
43	chr19:52150230-52150280	HRE	kidney:	n/a
44	chr19:52150634-52150684	HRE	kidney:	n/a
45	chr19:52134296-52134346	AG04449	skin:	fetal
46	chr19:52134393-52134443	HCM	heart:	n/a
47	chr19:52150634-52150684	Jurkat	blood:	n/a
48	chr19:52150634-52150684	HCT-116	colon:	n/a
49	chr19:52150634-52150684	T-47D	breast:	n/a
50	chr19:52133837-52133887	HAEpiC	amniotic membrane:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51975813..51976889-chr19:52140105..52142089,6	K562	blood:
2	chr19:52140352..52141294-chr19:52160036..52160673,2	K562	blood:
3	chr19:52050848..52053096-chr19:52143769..52145532,2	K562	blood:
4	chr19:51978649..51980839-chr19:52139351..52142005,2	K562	blood:
5	chr19:52123766..52126647-chr19:52131236..52133976,2	K562	blood:
6	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
7	chr19:52143293..52145764-chr19:52146395..52148250,2	K562	blood:
8	chr19:51960903..51963783-chr19:52139621..52141126,2	K562	blood:
9	chr19:52110923..52111673-chr19:52140530..52141292,3	MCF-7	breast:
10	chr19:52127522..52129415-chr19:52131096..52132777,2	K562	blood:
11	chr19:51924865..51925857-chr19:52140333..52141234,3	K562	blood:
12	chr19:52110942..52111788-chr19:52140328..52140831,2	K562	blood:
13	chr19:52017645..52019212-chr19:52145235..52147486,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIGLEC14-1	chr19:52133552-52133919	ENSG00000258669.1
2	lnc-SIGLEC14-1	chr19:52148730-52148798	ENSG00000258669.1
3	lnc-SIGLEC14-1	chr19:52133354-52133469	ENSG00000258669.1

No data

Variant related genes	Relation type
SIGLEC14	TF binding region
ENSG00000268500	TF binding region
RPL7P51	TF binding region
SIGLEC5	TF binding region
SIGLEC14	CpG island
ENSG00000268500	CpG island
RPL7P51	CpG island
SIGLEC5	CpG island
ENSG00000244071	chromatin interactions
ENSG00000105366	chromatin interactions
ENSG00000213822	chromatin interactions

Extended variants
information (count: 668 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369354553	chr19:52132440-52132441	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs563746519	chr19:52132444-52132445	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189514427	chr19:52132455-52132456	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112581861	chr19:52132524-52132525	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72330913	chr19:52132525-52132526	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549867211	chr19:52132528-52132529	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200122508	chr19:52132554-52132555	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568125989	chr19:52132556-52132557	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs71187699	chr19:52132558-52132559	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs113136987	chr19:52132565-52132566	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529117722	chr19:52132569-52132570	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547374162	chr19:52132573-52132574	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200569133	chr19:52132580-52132581	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371549495	chr19:52132586-52132587	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201585281	chr19:52132614-52132615	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs376678374	chr19:52132619-52132620	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566021929	chr19:52132620-52132621	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373250074	chr19:52132639-52132640	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34553740	chr19:52132668-52132669	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539755873	chr19:52132693-52132694	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552559234	chr19:52132699-52132700	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148006234	chr19:52132732-52132733	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs570881417	chr19:52132733-52132734	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537918447	chr19:52132740-52132741	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200210701	chr19:52132741-52132742	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs374818540	chr19:52132752-52132753	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574912773	chr19:52132756-52132757	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369175388	chr19:52132796-52132797	Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554032872	chr19:52132817-52132818	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572361362	chr19:52132951-52132952	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs111962315	chr19:52132964-52132965	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546090077	chr19:52132980-52132981	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2278832	chr19:52132986-52132987	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576000756	chr19:52133002-52133003	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543131875	chr19:52133005-52133006	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs561870658	chr19:52133036-52133037	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372451926	chr19:52133050-52133051	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs2278833	chr19:52133060-52133061	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117156027	chr19:52133070-52133071	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs375317816	chr19:52133075-52133076	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200820951	chr19:52133088-52133089	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201954824	chr19:52133098-52133099	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559592597	chr19:52133162-52133163	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533236117	chr19:52133168-52133169	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377628577	chr19:52133182-52133183	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs199864224	chr19:52133191-52133192	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs570741509	chr19:52133206-52133207	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374509897	chr19:52133213-52133214	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550003561	chr19:52133236-52133237	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376860084	chr19:52133241-52133242	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	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:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52125000-52133600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr19:52128800-52133800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr19:52130400-52132600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:52130800-52133200	Weak transcription	Gastric	stomach
5	chr19:52131000-52133800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr19:52131000-52134000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr19:52131400-52132600	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
8	chr19:52132400-52132600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr19:52132400-52132600	Active TSS	Primary B cells from cord blood	blood
10	chr19:52132400-52132600	Enhancers	Primary B cells from peripheral blood	blood
11	chr19:52132400-52132600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr19:52132400-52132600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:52132400-52132800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr19:52132400-52133600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr19:52132600-52132800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
16	chr19:52132600-52132800	Flanking Active TSS	Primary B cells from peripheral blood	blood
17	chr19:52132600-52133600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr19:52132600-52133800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr19:52132600-52133800	Weak transcription	Primary B cells from cord blood	blood
20	chr19:52132600-52133800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr19:52132600-52134600	Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr19:52132800-52133000	Enhancers	Primary B cells from peripheral blood	blood
23	chr19:52132800-52133800	Active TSS	Primary monocytes fromperipheralblood	blood
24	chr19:52132800-52133800	Active TSS	Monocytes-CD14+_RO01746	blood
25	chr19:52133000-52133400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr19:52133400-52133600	Enhancers	Primary B cells from peripheral blood	blood
27	chr19:52133600-52133800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
28	chr19:52133600-52134000	Enhancers	Primary hematopoietic stem cells	blood
29	chr19:52133600-52134000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr19:52133600-52134200	Flanking Active TSS	Primary B cells from peripheral blood	blood
31	chr19:52133800-52134000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr19:52133800-52134000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr19:52133800-52134200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
34	chr19:52133800-52134200	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr19:52133800-52134200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
36	chr19:52133800-52134200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr19:52133800-52134400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr19:52133800-52134600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr19:52133800-52135200	Enhancers	Placenta Amnion	Placenta Amnion
40	chr19:52133800-52136200	Enhancers	Placenta	Placenta
41	chr19:52134000-52134200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:52134200-52134400	Enhancers	Primary B cells from cord blood	blood
43	chr19:52134200-52134600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr19:52134200-52134600	Enhancers	Primary B cells from peripheral blood	blood
45	chr19:52134200-52134600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr19:52134200-52140200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr19:52134200-52144400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr19:52134400-52138000	Weak transcription	Primary B cells from cord blood	blood
49	chr19:52134600-52137800	Weak transcription	Primary B cells from peripheral blood	blood
50	chr19:52134600-52139400	Weak transcription	Primary monocytes fromperipheralblood	blood

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