Variant report

Variant	esv3394221
Chromosome Location	chr3:195673455-195681753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:629)
CpG islands
(count:245)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:195681353-195681596	K562	blood:	n/a	n/a
2	ATF2	chr3:195681259-195681587	GM12878	blood:	n/a	n/a
3	ATF3	chr3:195678739-195678871	K562	blood:	n/a	n/a
4	ATF3	chr3:195681303-195681452	K562	blood:	n/a	n/a
5	BATF	chr3:195681129-195681669	GM12878	blood:	n/a	n/a
6	BATF	chr3:195681681-195681957	GM12878	blood:	n/a	n/a
7	BATF	chr3:195680472-195680694	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:195680538-195680860	GM12878	blood:	n/a	chr3:195680659-195680668
9	BCL11A	chr3:195680283-195680924	GM12878	blood:	n/a	chr3:195680659-195680668
10	BCL11A	chr3:195679579-195679786	GM12878	blood:	n/a	chr3:195679673-195679680
11	BCL11A	chr3:195681171-195681812	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
12	BCL11A	chr3:195681118-195681900	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
13	BCL11A	chr3:195679437-195679731	GM12878	blood:	n/a	chr3:195679673-195679680
14	BCL3	chr3:195681285-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
15	BCLAF1	chr3:195681253-195681686	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
16	BCLAF1	chr3:195681279-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
17	BHLHE40	chr3:195681210-195681587	K562	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
18	BHLHE40	chr3:195681214-195681663	GM12878	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
19	BHLHE40	chr3:195681203-195681678	HepG2	liver:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
20	BRCA1	chr3:195681377-195681604	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr3:195681209-195681715	K562	blood:	n/a	n/a
22	CBX3	chr3:195681152-195682264	K562	blood:	n/a	n/a
23	CBX3	chr3:195679046-195679922	K562	blood:	n/a	n/a
24	CBX3	chr3:195680129-195680896	K562	blood:	n/a	n/a
25	CCNT2	chr3:195681222-195681599	K562	blood:	n/a	n/a
26	CEBPB	chr3:195681219-195681730	K562	blood:	n/a	n/a
27	CEBPB	chr3:195681244-195681840	GM12878	blood:	n/a	n/a
28	CEBPB	chr3:195680276-195680721	K562	blood:	n/a	n/a
29	CEBPB	chr3:195681388-195681580	Hela-S3	cervix:	n/a	n/a
30	CEBPD	chr3:195681081-195681739	K562	blood:	n/a	n/a
31	CHD1	chr3:195681413-195681628	GM12878	blood:	n/a	n/a
32	CHD2	chr3:195681301-195681610	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr3:195681358-195681608	GM12878	blood:	n/a	n/a
34	CREB1	chr3:195681295-195681566	GM12878	blood:	n/a	n/a
35	CREB1	chr3:195681284-195681534	GM12878	blood:	n/a	n/a
36	CREB1	chr3:195681318-195681559	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr3:195681297-195681526	HepG2	liver:	n/a	n/a
38	CREB1	chr3:195681317-195681541	HepG2	liver:	n/a	n/a
39	CREB1	chr3:195681328-195681466	A549	lung:	n/a	n/a
40	CREB1	chr3:195681268-195681489	A549	lung:	n/a	n/a
41	CREB1	chr3:195681296-195681494	K562	blood:	n/a	n/a
42	CREB1	chr3:195681315-195681561	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr3:195681279-195681557	K562	blood:	n/a	n/a
44	CTCF	chr3:195680846-195680861	LNCaP	prostate:	n/a	n/a
45	CTCF	chr3:195681417-195681479	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr3:195673510-195673575	GM10248	blood:	n/a	n/a
47	CTCF	chr3:195681355-195681484	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr3:195680825-195680912	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:195680865-195680897	LNCaP	prostate:	n/a	n/a
50	CTCF	chr3:195679589-195680056	K562	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195681400-195681450	AG09309	skin:	n/a
2	chr3:195681400-195681450	AG09309	skin:	n/a
3	chr3:195681091-195681141	GM19239	blood:	n/a
4	chr3:195678176-195678226	SK-N-SH_RA	brain:	n/a
5	chr3:195679450-195679500	HAEpiC	amniotic membrane:	n/a
6	chr3:195679450-195679500	NB4	blood:	n/a
7	chr3:195678176-195678226	IMR90	lung:	fetal
8	chr3:195678176-195678226	HIPEpiC	eye:	n/a
9	chr3:195681091-195681141	ProgFib	skin:	n/a
10	chr3:195679450-195679500	GM12878	blood:	n/a
11	chr3:195679450-195679500	HCM	heart:	n/a
12	chr3:195678176-195678226	AG04450	lung:	fetal
13	chr3:195679450-195679500	HepG2	liver:	n/a
14	chr3:195679450-195679500	CMK	blood:	n/a
15	chr3:195679450-195679500	SK-N-MC	brain:	n/a
16	chr3:195678176-195678226	HMEC	breast:	n/a
17	chr3:195679450-195679500	HUVEC	blood vessel:	n/a
18	chr3:195678176-195678226	NB4	blood:	n/a
19	chr3:195681400-195681450	HUVEC	blood vessel:	n/a
20	chr3:195681091-195681141	GM12892	blood:	n/a
21	chr3:195679450-195679500	T-47D	breast:	n/a
22	chr3:195678176-195678226	PrEC	prostate:	n/a
23	chr3:195681400-195681450	GM06990	blood:	n/a
24	chr3:195678176-195678226	BE2_C	brain:	n/a
25	chr3:195681091-195681141	IMR90	lung:	fetal
26	chr3:195681400-195681450	BE2_C	brain:	n/a
27	chr3:195678176-195678226	LNCaP	prostate:	n/a
28	chr3:195679450-195679500	K562	blood:	n/a
29	chr3:195678176-195678226	HRE	kidney:	n/a
30	chr3:195681091-195681141	T-47D	breast:	n/a
31	chr3:195681400-195681450	AG09319	gingival:	n/a
32	chr3:195681091-195681141	NHDF-neo	bronchial:	n/a
33	chr3:195678176-195678226	GM19239	blood:	n/a
34	chr3:195678176-195678226	ovcar-3	ovarian:	n/a
35	chr3:195679450-195679500	HL-60	blood:	n/a
36	chr3:195681400-195681450	CMK	blood:	n/a
37	chr3:195681400-195681450	HIPEpiC	eye:	n/a
38	chr3:195681400-195681450	MCF10A-Er-Src	breast:	n/a
39	chr3:195681091-195681141	MCF-7	breast:	n/a
40	chr3:195681400-195681450	HRPEpiC	eye:	n/a
41	chr3:195679450-195679500	MCF10A-Er-Src	breast:	n/a
42	chr3:195681400-195681450	ovcar-3	ovarian:	n/a
43	chr3:195678176-195678226	SK-N-MC	brain:	n/a
44	chr3:195681400-195681450	MCF-7	breast:	n/a
45	chr3:195681400-195681450	SKMC	muscle:	n/a
46	chr3:195681091-195681141	NT2-D1	testis:	n/a
47	chr3:195681091-195681141	HepG2	liver:	n/a
48	chr3:195681400-195681450	AG10803	skin:	n/a
49	chr3:195678176-195678226	HRCEpiC	kidney:	n/a
50	chr3:195681400-195681450	RPTEC	kidney:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195639677..195641924-chr3:195679365..195681428,2	MCF-7	breast:
2	chr3:195620748..195623055-chr3:195679886..195681403,2	K562	blood:
3	chr3:195673861..195675995-chr5:278201..279705,3	K562	blood:
4	chr3:195636473..195638760-chr3:195679951..195681488,2	MCF-7	breast:
5	chr3:195679870..195682569-chr3:197379763..197382610,2	K562	blood:
6	chr3:195361738..195362245-chr3:195681393..195681916,2	HCT-116	colon:
7	chr3:195361732..195362263-chr3:195681373..195681896,2	MCF-7	breast:
8	chr3:195645901..195648267-chr3:195679890..195681479,3	MCF-7	breast:
9	chr3:195679874..195682569-chr3:197381110..197382679,2	K562	blood:
10	chr3:195620748..195623057-chr3:195678515..195681386,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-2	chr3:195673684-195674350	NONHSAT094275
2	lnc-TNK2-2	chr3:195676059-195679566	ENSG00000260261.1
3	lnc-MUC20-9	chr3:195674996-195675559	NONHSAT094276
4	lnc-TNK2-2	chr3:195674206-195674576	NONHSAT094271
5	lnc-TNK2-2	chr3:195676113-195676284	NONHSAT094275

No data

Variant related genes	Relation type
ENSG00000260261	TF binding region
ENSG00000260261	CpG island
ENSG00000266730	chromatin interactions
ENSG00000061938	chromatin interactions
ENSG00000273009	chromatin interactions

Extended variants
information (count: 423 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1679295	chr3:195673470-195673471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183279789	chr3:195673491-195673492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566463514	chr3:195673501-195673502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563942760	chr3:195673508-195673509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78789590	chr3:195673524-195673525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187811812	chr3:195673525-195673526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193167538	chr3:195673532-195673533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549311416	chr3:195673536-195673537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185051450	chr3:195673539-195673540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62285294	chr3:195673540-195673541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575794699	chr3:195673543-195673544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4037317	chr3:195673557-195673558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200325964	chr3:195673559-195673560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201007950	chr3:195673563-195673564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377095759	chr3:195673564-195673565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374995878	chr3:195673574-195673575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538038772	chr3:195673576-195673577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199745169	chr3:195673607-195673608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371463960	chr3:195673639-195673640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374734298	chr3:195673642-195673643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113344171	chr3:195673663-195673664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368461247	chr3:195673712-195673713	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs28759193	chr3:195673738-195673739	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
24	rs559054999	chr3:195673741-195673742	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs556440414	chr3:195673791-195673792	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs200837474	chr3:195673817-195673818	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
27	rs12486126	chr3:195673867-195673868	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
28	rs188997171	chr3:195673883-195673884	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs74489788	chr3:195673914-195673915	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs28574755	chr3:195673925-195673926	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
31	rs12489913	chr3:195673933-195673934	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531174436	chr3:195673946-195673947	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
33	rs79189515	chr3:195673949-195673950	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
34	rs192634373	chr3:195673950-195673951	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
35	rs3827579	chr3:195673953-195673954	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs12490741	chr3:195673955-195673956	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
37	rs3827577	chr3:195673966-195673967	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
38	rs3827576	chr3:195673968-195673969	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
39	rs534973415	chr3:195673970-195673971	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
40	rs112829251	chr3:195673992-195673993	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
41	rs553355697	chr3:195673998-195673999	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
42	rs3827574	chr3:195674000-195674001	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
43	rs3827573	chr3:195674023-195674024	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs201657060	chr3:195674043-195674044	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs538758676	chr3:195674046-195674047	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs3827570	chr3:195674063-195674064	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs575334389	chr3:195674089-195674090	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs200014483	chr3:195674090-195674091	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs6801647	chr3:195674107-195674108	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs202220668	chr3:195674108-195674109	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195647200-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:195648600-195680600	Weak transcription	Pancreas	Pancrea
3	chr3:195651800-195673800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:195656600-195681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:195656800-195676400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr3:195656800-195679400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr3:195657800-195681400	Weak transcription	GM12878-XiMat	blood
8	chr3:195659000-195676400	Weak transcription	Hela-S3	cervix
9	chr3:195659600-195681200	Weak transcription	Brain Hippocampus Middle	brain
10	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
11	chr3:195660000-195681200	Weak transcription	Colonic Mucosa	Colon
12	chr3:195660400-195680600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr3:195660600-195681200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr3:195661200-195681000	Weak transcription	Ovary	ovary
15	chr3:195661800-195681200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:195663400-195681200	Weak transcription	Left Ventricle	heart
17	chr3:195663600-195673800	Weak transcription	Liver	Liver
18	chr3:195663600-195681000	Weak transcription	Fetal Brain Female	brain
19	chr3:195663600-195681200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:195663600-195681200	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr3:195663800-195682000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr3:195664400-195681200	Weak transcription	Osteobl	bone
23	chr3:195665000-195681200	Weak transcription	Placenta	Placenta
24	chr3:195665200-195677800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
26	chr3:195665400-195681400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr3:195665400-195685200	Weak transcription	Aorta	Aorta
28	chr3:195666000-195677200	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr3:195666000-195677800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr3:195667200-195681200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr3:195667400-195677200	Weak transcription	Gastric	stomach
32	chr3:195667400-195677200	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr3:195667400-195680800	Weak transcription	Right Ventricle	heart
34	chr3:195667400-195681200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:195667400-195681200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:195667400-195681200	Weak transcription	Brain Anterior Caudate	brain
37	chr3:195667400-195681200	Weak transcription	Brain Cingulate Gyrus	brain
38	chr3:195667400-195681200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr3:195667400-195681200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:195667400-195681400	Weak transcription	Primary B cells from peripheral blood	blood
41	chr3:195667400-195681400	Weak transcription	Brain Substantia Nigra	brain
42	chr3:195667400-195684200	Weak transcription	Spleen	Spleen
43	chr3:195667400-195686200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr3:195667600-195677600	Weak transcription	Primary T cells from cord blood	blood
45	chr3:195667600-195680200	Weak transcription	Fetal Stomach	stomach
46	chr3:195667600-195681200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:195667600-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:195667600-195681200	Weak transcription	Esophagus	oesophagus
49	chr3:195667600-195681400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr3:195667600-195681600	Weak transcription	Fetal Intestine Large	intestine

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