Variant report

Variant	nsv900847
Chromosome Location	chr13:89788636-89873873
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:122)
Chromatin interactive
region (count:1)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr13:89809033-89809039	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr13:89788283-89788664	HepG2	liver:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
3	CEBPB	chr13:89811087-89811294	IMR90	lung:	n/a	n/a
4	CEBPB	chr13:89856664-89857107	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
5	CEBPB	chr13:89856691-89857129	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
6	CEBPB	chr13:89788021-89788642	Hela-S3	cervix:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
7	CEBPB	chr13:89816073-89816273	HepG2	liver:	n/a	chr13:89816134-89816145 chr13:89816156-89816167
8	CEBPB	chr13:89870206-89870527	HepG2	liver:	n/a	chr13:89870358-89870367 chr13:89870358-89870369 chr13:89870356-89870367
9	CEBPB	chr13:89823580-89823834	HepG2	liver:	n/a	chr13:89823710-89823721
10	CTCF	chr13:89873440-89873590	WERI-Rb-1	eye:	n/a	n/a
11	CUX1	chr13:89793933-89794023	GM12878	blood:	n/a	n/a
12	E2F4	chr13:89862284-89862740	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr13:89856319-89856519	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr13:89800879-89801240	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr13:89858454-89858750	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr13:89797098-89797372	MCF10A-Er-Src	breast:	n/a	n/a
17	EBF1	chr13:89788671-89788801	GM12878	blood:	n/a	chr13:89788774-89788785
18	EBF1	chr13:89789874-89789897	GM12878	blood:	n/a	n/a
19	EBF1	chr13:89789130-89789467	GM12878	blood:	n/a	chr13:89789322-89789333
20	EP300	chr13:89856582-89857113	ECC-1	luminal epithelium:	n/a	chr13:89856961-89856971
21	EP300	chr13:89834322-89834358	Hela-S3	cervix:	n/a	n/a
22	EP300	chr13:89856527-89857222	ECC-1	luminal epithelium:	n/a	chr13:89856961-89856971
23	FOS	chr13:89797902-89798134	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr13:89797882-89798173	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr13:89851249-89851730	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr13:89851357-89851651	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr13:89797935-89798204	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr13:89797836-89798141	MCF10A-Er-Src	breast:	n/a	n/a
29	FOXA1	chr13:89815452-89815761	T-47D	breast:	n/a	n/a
30	FOXA1	chr13:89864463-89864714	T-47D	breast:	n/a	chr13:89864608-89864623
31	FOXA1	chr13:89864485-89864812	T-47D	breast:	n/a	chr13:89864608-89864623
32	FOXM1	chr13:89856497-89857158	ECC-1	luminal epithelium:	n/a	n/a
33	FOXM1	chr13:89856553-89857286	ECC-1	luminal epithelium:	n/a	n/a
34	GABPA	chr13:89815389-89815831	MCF-7	breast:	n/a	n/a
35	GATA3	chr13:89864459-89864800	T-47D	breast:	n/a	chr13:89864633-89864641
36	GATA3	chr13:89856112-89856312	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr13:89789948-89790148	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr13:89864404-89864735	T-47D	breast:	n/a	chr13:89864633-89864641
39	JUN	chr13:89857089-89857287	HepG2	liver:	n/a	chr13:89857197-89857210
40	JUND	chr13:89867705-89867868	HepG2	liver:	n/a	chr13:89867736-89867747
41	JUND	chr13:89857032-89857301	HepG2	liver:	n/a	n/a
42	JUND	chr13:89797852-89798157	HepG2	liver:	n/a	chr13:89798008-89798019
43	KAP1	chr13:89802259-89802782	HEK293	kidney:	n/a	n/a
44	KAP1	chr13:89873637-89874352	HEK293	kidney:	n/a	n/a
45	MAFF	chr13:89802007-89802250	HepG2	liver:	n/a	chr13:89802128-89802146
46	MAFF	chr13:89795075-89795330	HepG2	liver:	n/a	n/a
47	MAFK	chr13:89792332-89792358	Hela-S3	cervix:	n/a	n/a
48	MAFK	chr13:89801961-89802303	HepG2	liver:	n/a	chr13:89802129-89802144
49	MAFK	chr13:89795041-89795276	HepG2	liver:	n/a	chr13:89795150-89795164 chr13:89795152-89795163
50	MAFK	chr13:89795042-89795299	HepG2	liver:	n/a	chr13:89795150-89795164 chr13:89795152-89795163

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89815451-89815501	BJ	skin:	n/a
2	chr13:89815421-89815471	HRE	kidney:	n/a
3	chr13:89815421-89815471	HUVEC	blood vessel:	n/a
4	chr13:89815421-89815471	NB4	blood:	n/a
5	chr13:89815421-89815471	AoSMC	blood vessel:	n/a
6	chr13:89815421-89815471	PANC-1	pancreas:	n/a
7	chr13:89815421-89815471	SKMC	muscle:	n/a
8	chr13:89815451-89815501	HUVEC	blood vessel:	n/a
9	chr13:89815421-89815471	NHBE	bronchial:	n/a
10	chr13:89815421-89815471	ovcar-3	ovarian:	n/a
11	chr13:89815451-89815501	T-47D	breast:	n/a
12	chr13:89815451-89815501	AoSMC	blood vessel:	n/a
13	chr13:89815421-89815471	H1-hESC	embryonic stem cell:	embryo
14	chr13:89815421-89815471	RPTEC	kidney:	n/a
15	chr13:89815421-89815471	HAEpiC	amniotic membrane:	n/a
16	chr13:89815421-89815471	AG09309	skin:	n/a
17	chr13:89815451-89815501	HCPEpiC	choroid plexus:	n/a
18	chr13:89815421-89815471	NT2-D1	testis:	n/a
19	chr13:89815451-89815501	A549	lung:	n/a
20	chr13:89815451-89815501	HAEpiC	amniotic membrane:	n/a
21	chr13:89815421-89815471	SK-N-SH	brain:	n/a
22	chr13:89815451-89815501	SAEC	small airway:	n/a
23	chr13:89815421-89815471	AG09319	gingival:	n/a
24	chr13:89815421-89815471	HMEC	breast:	n/a
25	chr13:89815421-89815471	HCM	heart:	n/a
26	chr13:89815451-89815501	HCT-116	colon:	n/a
27	chr13:89815451-89815501	HNPCEpiC	eye:	n/a
28	chr13:89815451-89815501	AG04450	lung:	fetal
29	chr13:89815451-89815501	Jurkat	blood:	n/a
30	chr13:89815451-89815501	HEK293	kidney:	embryo
31	chr13:89815421-89815471	HNPCEpiC	eye:	n/a
32	chr13:89815451-89815501	GM06990	blood:	n/a
33	chr13:89815451-89815501	PrEC	prostate:	n/a
34	chr13:89815421-89815471	A549	lung:	n/a
35	chr13:89815451-89815501	SK-N-SH_RA	brain:	n/a
36	chr13:89815421-89815471	MCF10A-Er-Src	breast:	n/a
37	chr13:89815451-89815501	LNCaP	prostate:	n/a
38	chr13:89815451-89815501	PANC-1	pancreas:	n/a
39	chr13:89815451-89815501	HL-60	blood:	n/a
40	chr13:89815421-89815471	SAEC	small airway:	n/a
41	chr13:89815451-89815501	HRE	kidney:	n/a
42	chr13:89815451-89815501	U87	brain:	n/a
43	chr13:89815451-89815501	AG04449	skin:	fetal
44	chr13:89815451-89815501	GM12878	blood:	n/a
45	chr13:89815421-89815471	GM12892	blood:	n/a
46	chr13:89815421-89815471	HRPEpiC	eye:	n/a
47	chr13:89815451-89815501	SKMC	muscle:	n/a
48	chr13:89815451-89815501	GM12891	blood:	n/a
49	chr13:89815421-89815471	U87	brain:	n/a
50	chr13:89815451-89815501	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
2	lnc-SLITRK6-10	chr13:89867150-89867581	ENSG00000232225.2
3	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
4	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
5	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
6	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
7	lnc-SLITRK6-10	chr13:89867101-89867581	ENSG00000232225.2
8	lnc-SLITRK6-10	chr13:89871826-89871963	XLOC_010684
9	lnc-SLITRK6-10	chr13:89871825-89871963	ENSG00000232225.2
10	lnc-SLITRK6-10	chr13:89867150-89867581	XLOC_010684
11	lnc-SLITRK6-10	chr13:89867101-89867581	XLOC_010684
12	lnc-SLITRK6-10	chr13:89868228-89868395	ENSG00000232225.2
13	lnc-SLITRK6-24	chr13:89811759-89811902	NONHSAT034620
14	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
15	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
16	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
17	lnc-SLITRK6-24	chr13:89815360-89815434	NONHSAT034620
18	lnc-SLITRK6-10	chr13:89868228-89868395	XLOC_010684

No data

Variant related genes	Relation type
LINC01047	TF binding region
LINC01047	CpG island
RTF1	miRNA target sites
RTKN	miRNA target sites
RTCD1	miRNA target sites

Extended variants
information (count: 621 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538988214	chr13:89788815-89788816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568769008	chr13:89788863-89788864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534239563	chr13:89788878-89788879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141955414	chr13:89788891-89788892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147319598	chr13:89788925-89788926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34844165	chr13:89788940-89788941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73589073	chr13:89788961-89788962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs145016418	chr13:89788964-89788965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34366982	chr13:89788976-89788977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71212960	chr13:89788979-89788980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34498546	chr13:89788981-89788982	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9583658	chr13:89788982-89788983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528360613	chr13:89788997-89788998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552903885	chr13:89789006-89789007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554758439	chr13:89789056-89789057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551619931	chr13:89789066-89789067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564787021	chr13:89789111-89789112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562973685	chr13:89789190-89789191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2253547	chr13:89811760-89811761	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186389	chr13:89811772-89811773	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs187053224	chr13:89811817-89811818	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs138016542	chr13:89811848-89811849	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs527375145	chr13:89813809-89813810	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs314386	chr13:89813913-89813914	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570545603	chr13:89813918-89813919	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs117092295	chr13:89813929-89813930	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs314387	chr13:89813937-89813938	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs78664868	chr13:89813944-89813945	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs535789977	chr13:89813964-89813965	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs553929307	chr13:89813996-89813997	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566916133	chr13:89814002-89814003	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs572101060	chr13:89814018-89814019	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539628613	chr13:89814044-89814045	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs558747622	chr13:89814047-89814048	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs149834899	chr13:89814156-89814157	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs141003416	chr13:89814165-89814166	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs68014328	chr13:89814167-89814168	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs548703948	chr13:89814168-89814169	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs398117699	chr13:89814171-89814172	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs535932508	chr13:89814217-89814218	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs184375588	chr13:89814218-89814219	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532511436	chr13:89814232-89814233	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs574780840	chr13:89814281-89814282	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs141993785	chr13:89814298-89814299	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs376403981	chr13:89814299-89814300	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs377134884	chr13:89814308-89814309	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs552697830	chr13:89814318-89814319	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181269360	chr13:89814321-89814322	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs182605	chr13:89814343-89814344	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs370024595	chr13:89814370-89814371	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Burkitt''s lymphoma	19759907	CNVD
Autism	20841430	CNVD
Wilms tumour	21544195	CNVD

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89788800-89789200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr13:89813800-89816000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:89815000-89815600	Active TSS	Placenta	Placenta
4	chr13:89815200-89815800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:89822000-89822600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:89822200-89822600	Enhancers	Adipose Nuclei	Adipose
7	chr13:89822200-89822600	Enhancers	Fetal Heart	heart
8	chr13:89850800-89851200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr13:89850800-89851400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:89850800-89851400	Enhancers	HMEC	breast
11	chr13:89850800-89851400	Enhancers	NHEK	skin
12	chr13:89850800-89852400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr13:89851200-89852200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr13:89851400-89851800	Flanking Active TSS	NHEK	skin
15	chr13:89851400-89852000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr13:89851800-89852800	Enhancers	NHEK	skin
17	chr13:89852000-89852200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr13:89852200-89852800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr13:89852800-89857200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr13:89857200-89858000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr13:89858000-89858600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr13:89858000-89858600	Enhancers	Fetal Lung	lung
23	chr13:89858200-89858600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr13:89860400-89861200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr13:89865800-89867600	Enhancers	Fetal Lung	lung
26	chr13:89866600-89867600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr13:89873400-89875000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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