Variant report

Variant	nsv960830
Chromosome Location	chr19:36447942-36451207
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:36450146-36450182	K562	blood:	n/a	n/a
2	BACH1	chr19:36450615-36451065	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr19:36449804-36450338	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr19:36449999-36450254	GM12878	blood:	n/a	n/a
5	CCNT2	chr19:36450008-36450230	K562	blood:	n/a	n/a
6	CREB1	chr19:36449854-36450376	GM12878	blood:	n/a	n/a
7	CREB1	chr19:36450749-36451177	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr19:36449864-36450365	A549	lung:	n/a	n/a
9	CTCF	chr19:36450020-36450170	HCM	heart:	n/a	chr19:36450113-36450126
10	CTCF	chr19:36450040-36450190	HPAF	blood vessel:	n/a	chr19:36450113-36450126
11	CTCF	chr19:36450068-36450226	Kidney_OC	kidney:	n/a	chr19:36450113-36450126
12	CTCF	chr19:36449942-36450266	A549	lung:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
13	CTCF	chr19:36450000-36450150	HRE	kidney:	n/a	chr19:36450113-36450126
14	CTCF	chr19:36449980-36450318	Spleen_OC	spleen:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
15	CTCF	chr19:36449997-36450264	HepG2	liver:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
16	CTCF	chr19:36450005-36450297	MCF-7	breast:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
17	CTCF	chr19:36450080-36450230	HPF	lung:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
18	CTCF	chr19:36450080-36450230	AG09309	skin:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
19	CTCF	chr19:36450080-36450230	K562	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
20	CTCF	chr19:36450160-36450310	GM12868	blood:	n/a	chr19:36450212-36450230 chr19:36450219-36450227
21	CTCF	chr19:36450009-36450251	Pancreas_OC	pancreas:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
22	CTCF	chr19:36450060-36450210	AG09309	skin:	n/a	chr19:36450113-36450126
23	CTCF	chr19:36449984-36450334	Fibrobl	skin:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
24	CTCF	chr19:36450018-36450277	MCF-7	breast:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
25	CTCF	chr19:36450017-36450301	GM12878	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
26	CTCF	chr19:36450120-36450270	HL-60	blood:	n/a	chr19:36450212-36450230 chr19:36450219-36450227
27	CTCF	chr19:36450140-36450290	GM12878	blood:	n/a	chr19:36450212-36450230 chr19:36450219-36450227
28	CTCF	chr19:36450040-36450190	GM12875	blood:	n/a	chr19:36450113-36450126
29	CTCF	chr19:36450100-36450250	GM12867	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
30	CTCF	chr19:36450100-36450250	HFF-Myc	foreskin:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
31	CTCF	chr19:36449988-36450309	Gliobla	brain:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
32	CTCF	chr19:36450020-36450170	HAc	cerebellar:	n/a	chr19:36450113-36450126
33	CTCF	chr19:36450080-36450230	GM12866	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
34	CTCF	chr19:36449690-36450457	SK-N-SH	brain:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
35	CTCF	chr19:36450040-36450190	K562	blood:	n/a	chr19:36450113-36450126
36	CTCF	chr19:36450040-36450190	AG04450	lung:	n/a	chr19:36450113-36450126
37	CTCF	chr19:36450005-36450290	K562	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
38	CTCF	chr19:36450100-36450250	HRE	kidney:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
39	CTCF	chr19:36450060-36450210	AG04450	lung:	n/a	chr19:36450113-36450126
40	CTCF	chr19:36449992-36450311	GM19238	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
41	CTCF	chr19:36450120-36450270	HFF-Myc	foreskin:	n/a	chr19:36450212-36450230 chr19:36450219-36450227
42	CTCF	chr19:36450620-36450770	K562	blood:	n/a	n/a
43	CTCF	chr19:36450080-36450230	HRPEpiC	eye:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
44	CTCF	chr19:36450179-36450241	HepG2	liver:	n/a	chr19:36450212-36450230 chr19:36450219-36450227
45	CTCF	chr19:36450120-36450270	GM12875	blood:	n/a	chr19:36450212-36450230 chr19:36450219-36450227
46	CTCF	chr19:36449979-36450348	GM19239	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227
47	CTCF	chr19:36450060-36450210	GM12867	blood:	n/a	chr19:36450113-36450126
48	CTCF	chr19:36450320-36450470	AG09309	skin:	n/a	n/a
49	CTCF	chr19:36450060-36450210	HCPEpiC	choroid plexus:	n/a	chr19:36450113-36450126
50	CTCF	chr19:36450011-36450298	GM13976	blood:	n/a	chr19:36450113-36450126 chr19:36450212-36450230 chr19:36450219-36450227

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36450121-36450171	A549	lung:	n/a
2	chr19:36450528-36450578	BE2_C	brain:	n/a
3	chr19:36450215-36450265	HCT-116	colon:	n/a
4	chr19:36449803-36449853	U87	brain:	n/a
5	chr19:36449803-36449853	GM19239	blood:	n/a
6	chr19:36450358-36450408	HRE	kidney:	n/a
7	chr19:36450896-36450946	LNCaP	prostate:	n/a
8	chr19:36450121-36450171	Caco-2	colon:	n/a
9	chr19:36450528-36450578	Hepatocyte	liver:	n/a
10	chr19:36450896-36450946	NB4	blood:	n/a
11	chr19:36450215-36450265	U87	brain:	n/a
12	chr19:36450215-36450265	SK-N-SH	brain:	n/a
13	chr19:36450896-36450946	Caco-2	colon:	n/a
14	chr19:36449803-36449853	MCF10A-Er-Src	breast:	n/a
15	chr19:36450916-36450966	AG09319	gingival:	n/a
16	chr19:36449875-36449925	Hela-S3	cervix:	n/a
17	chr19:36449875-36449925	GM12878	blood:	n/a
18	chr19:36450358-36450408	PANC-1	pancreas:	n/a
19	chr19:36449803-36449853	HAEpiC	amniotic membrane:	n/a
20	chr19:36449803-36449853	K562	blood:	n/a
21	chr19:36450916-36450966	A549	lung:	n/a
22	chr19:36449803-36449853	ProgFib	skin:	n/a
23	chr19:36450528-36450578	CMK	blood:	n/a
24	chr19:36450528-36450578	Jurkat	blood:	n/a
25	chr19:36450916-36450966	SK-N-SH_RA	brain:	n/a
26	chr19:36450916-36450966	GM12892	blood:	n/a
27	chr19:36449875-36449925	AG09309	skin:	n/a
28	chr19:36450358-36450408	HCM	heart:	n/a
29	chr19:36450916-36450966	HUVEC	blood vessel:	n/a
30	chr19:36449803-36449853	GM12892	blood:	n/a
31	chr19:36450358-36450408	BE2_C	brain:	n/a
32	chr19:36450896-36450946	AG09319	gingival:	n/a
33	chr19:36450358-36450408	GM12892	blood:	n/a
34	chr19:36449803-36449853	SK-N-SH	brain:	n/a
35	chr19:36449875-36449925	HCM	heart:	n/a
36	chr19:36450358-36450408	NHDF-neo	bronchial:	n/a
37	chr19:36450358-36450408	HRPEpiC	eye:	n/a
38	chr19:36450528-36450578	LNCaP	prostate:	n/a
39	chr19:36450896-36450946	HIPEpiC	eye:	n/a
40	chr19:36450215-36450265	NB4	blood:	n/a
41	chr19:36450528-36450578	ovcar-3	ovarian:	n/a
42	chr19:36450896-36450946	Hepatocyte	liver:	n/a
43	chr19:36449875-36449925	CMK	blood:	n/a
44	chr19:36450358-36450408	HEEpiC	esophagus:	n/a
45	chr19:36450916-36450966	HCT-116	colon:	n/a
46	chr19:36449803-36449853	HUVEC	blood vessel:	n/a
47	chr19:36449875-36449925	AG04450	lung:	fetal
48	chr19:36450121-36450171	Hepatocyte	liver:	n/a
49	chr19:36450358-36450408	NH-A	brain:	n/a
50	chr19:36450215-36450265	MCF-7	breast:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRFN3-3	chr19:36449901-36450094	ENSG00000267786.1
2	lnc-LRFN3-3	chr19:36449116-36449177	ENSG00000267786.1
3	lnc-C19orf46-2	chr19:36448023-36448284	NONHSAT065943
4	lnc-LRFN3-3	chr19:36448155-36448266	ENSG00000267786.1

Variant related genes	Relation type
ENSG00000267388	TF binding region
ENSG00000267113	TF binding region
ENSG00000267388	CpG island
ENSG00000267113	CpG island

Extended variants
information (count: 100 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13346231	chr19:36448006-36448007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528288839	chr19:36448016-36448017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546854269	chr19:36448026-36448027	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs568329382	chr19:36448082-36448083	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs535411849	chr19:36448091-36448092	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs557243785	chr19:36448107-36448108	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs192836214	chr19:36448163-36448164	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs539452445	chr19:36448165-36448166	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs56009137	chr19:36448174-36448175	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs557828778	chr19:36448189-36448190	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs28675882	chr19:36448272-36448273	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs386808967	chr19:36448291-36448292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73928370	chr19:36448294-36448295	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555571863	chr19:36448300-36448301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574200617	chr19:36448308-36448309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11880325	chr19:36448334-36448335	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs563204240	chr19:36448365-36448366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35742682	chr19:36448398-36448399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs397768211	chr19:36448411-36448412	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575081846	chr19:36448414-36448415	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34915088	chr19:36448509-36448510	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564158240	chr19:36448545-36448546	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185774752	chr19:36448565-36448566	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147325869	chr19:36448638-36448639	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79698216	chr19:36448731-36448732	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532471436	chr19:36448732-36448733	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529099714	chr19:36448741-36448742	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367903055	chr19:36448797-36448798	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550555603	chr19:36448833-36448834	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4806238	chr19:36448842-36448843	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539438349	chr19:36448863-36448864	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551395652	chr19:36448889-36448890	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11673051	chr19:36448921-36448922	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77084233	chr19:36448934-36448935	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142980630	chr19:36448983-36448984	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577172579	chr19:36449011-36449012	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572863253	chr19:36449084-36449085	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190504275	chr19:36449125-36449126	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs544862440	chr19:36449135-36449136	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs538435442	chr19:36449146-36449147	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs150814723	chr19:36449178-36449179	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs578224715	chr19:36449216-36449217	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545797476	chr19:36449261-36449262	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564098926	chr19:36449336-36449337	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs572897421	chr19:36449344-36449345	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs79509161	chr19:36449350-36449351	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs561830405	chr19:36449501-36449502	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs112818730	chr19:36449506-36449507	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs563054735	chr19:36449569-36449570	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs193239016	chr19:36449654-36449655	Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36430000-36450000	Weak transcription	Right Atrium	heart
2	chr19:36436200-36449000	Weak transcription	Spleen	Spleen
3	chr19:36436600-36448200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:36445000-36448000	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr19:36445000-36449600	Enhancers	Primary T cells fromperipheralblood	blood
6	chr19:36445200-36449600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr19:36446600-36448400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr19:36446600-36449000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:36446800-36449200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr19:36447000-36448800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr19:36447000-36449000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr19:36447200-36448200	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr19:36447200-36448400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr19:36447200-36448800	Weak transcription	Primary T cells from cord blood	blood
15	chr19:36447200-36448800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr19:36447400-36449000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr19:36447400-36449200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr19:36447800-36448800	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr19:36448000-36448400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr19:36448200-36449600	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr19:36448400-36449400	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr19:36448400-36449600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr19:36448400-36449800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
24	chr19:36448800-36449200	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:36448800-36449400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr19:36448800-36449600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr19:36448800-36449800	Enhancers	Primary T cells from cord blood	blood
28	chr19:36448800-36449800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr19:36449000-36449200	Enhancers	Spleen	Spleen
30	chr19:36449000-36449800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr19:36449000-36449800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr19:36449000-36449800	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr19:36449000-36450000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr19:36449000-36451000	Bivalent Enhancer	Placenta	Placenta
35	chr19:36449200-36449400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:36449200-36449400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr19:36449200-36449400	Bivalent Enhancer	Fetal Brain Female	brain
38	chr19:36449200-36449400	Bivalent Enhancer	Thymus	Thymus
39	chr19:36449200-36449800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr19:36449200-36450000	Weak transcription	Spleen	Spleen
41	chr19:36449200-36450600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr19:36449400-36449600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
43	chr19:36449400-36449800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:36449400-36450000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr19:36449400-36450000	Bivalent Enhancer	Fetal Thymus	thymus
46	chr19:36449400-36451000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr19:36449400-36451200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr19:36449600-36449800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr19:36449600-36450000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
50	chr19:36449600-36450000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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