Variant report

Variant	esv3487234
Chromosome Location	chr3:195664550-195724142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1871)
CpG islands
(count:1831)
Chromatin interactive
region (count:15)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1871 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195687778-195688031	K562	blood:	n/a	n/a
2	ATF1	chr3:195681353-195681596	K562	blood:	n/a	n/a
3	ATF2	chr3:195681259-195681587	GM12878	blood:	n/a	n/a
4	ATF3	chr3:195717483-195717694	K562	blood:	n/a	n/a
5	ATF3	chr3:195717067-195717371	A549	lung:	n/a	n/a
6	ATF3	chr3:195681303-195681452	K562	blood:	n/a	n/a
7	ATF3	chr3:195717164-195717371	K562	blood:	n/a	n/a
8	ATF3	chr3:195717064-195717382	K562	blood:	n/a	n/a
9	ATF3	chr3:195678739-195678871	K562	blood:	n/a	n/a
10	BACH1	chr3:195717045-195717538	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:195705475-195705667	GM12878	blood:	n/a	chr3:195705640-195705649 chr3:195705599-195705610
12	BATF	chr3:195688640-195688926	GM12878	blood:	n/a	n/a
13	BATF	chr3:195682771-195683491	GM12878	blood:	n/a	n/a
14	BATF	chr3:195680472-195680694	GM12878	blood:	n/a	n/a
15	BATF	chr3:195717540-195717834	GM12878	blood:	n/a	n/a
16	BATF	chr3:195715731-195716052	GM12878	blood:	n/a	n/a
17	BATF	chr3:195716145-195716590	GM12878	blood:	n/a	n/a
18	BATF	chr3:195681681-195681957	GM12878	blood:	n/a	n/a
19	BATF	chr3:195682768-195683488	GM12878	blood:	n/a	n/a
20	BATF	chr3:195681129-195681669	GM12878	blood:	n/a	n/a
21	BATF	chr3:195717279-195717490	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:195716071-195717206	GM12878	blood:	n/a	chr3:195716811-195716824 chr3:195716792-195716801 chr3:195716946-195716959
23	BCL11A	chr3:195722372-195722606	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:195711556-195711737	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:195723014-195723259	GM12878	blood:	n/a	chr3:195723080-195723089
26	BCL11A	chr3:195681860-195682057	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:195717296-195717514	GM12878	blood:	n/a	chr3:195717473-195717482
28	BCL11A	chr3:195680538-195680860	GM12878	blood:	n/a	chr3:195680659-195680668
29	BCL11A	chr3:195679437-195679731	GM12878	blood:	n/a	chr3:195679673-195679680
30	BCL11A	chr3:195682872-195683277	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:195679579-195679786	GM12878	blood:	n/a	chr3:195679673-195679680
32	BCL11A	chr3:195680283-195680924	GM12878	blood:	n/a	chr3:195680659-195680668
33	BCL11A	chr3:195682895-195683356	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:195717225-195717865	GM12878	blood:	n/a	chr3:195717473-195717482
35	BCL11A	chr3:195681118-195681900	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
36	BCL11A	chr3:195681171-195681812	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
37	BCL11A	chr3:195715512-195715842	GM12878	blood:	n/a	n/a
38	BCL3	chr3:195681285-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
39	BCL3	chr3:195700608-195700811	GM12878	blood:	n/a	n/a
40	BCLAF1	chr3:195681253-195681686	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
41	BCLAF1	chr3:195681279-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
42	BHLHE40	chr3:195717520-195717617	K562	blood:	n/a	n/a
43	BHLHE40	chr3:195717244-195717251	K562	blood:	n/a	n/a
44	BHLHE40	chr3:195681203-195681678	HepG2	liver:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
45	BHLHE40	chr3:195681214-195681663	GM12878	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
46	BHLHE40	chr3:195681210-195681587	K562	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
47	BRCA1	chr3:195681377-195681604	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr3:195716251-195717942	K562	blood:	n/a	n/a
49	CBX3	chr3:195721219-195721517	K562	blood:	n/a	n/a
50	CBX3	chr3:195679046-195679922	K562	blood:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195681400-195681450	AG04450	lung:	fetal
2	chr3:195681400-195681450	AG04450	lung:	fetal
3	chr3:195716632-195716682	BJ	skin:	n/a
4	chr3:195682326-195682376	BE2_C	brain:	n/a
5	chr3:195717416-195717466	Hela-S3	cervix:	n/a
6	chr3:195709698-195709748	GM12891	blood:	n/a
7	chr3:195717962-195718012	HCT-116	colon:	n/a
8	chr3:195719262-195719312	HCF	heart:	n/a
9	chr3:195683635-195683685	CMK	blood:	n/a
10	chr3:195714100-195714150	LNCaP	prostate:	n/a
11	chr3:195679450-195679500	RPTEC	kidney:	n/a
12	chr3:195681091-195681141	HCPEpiC	choroid plexus:	n/a
13	chr3:195679450-195679500	HRCEpiC	kidney:	n/a
14	chr3:195682365-195682415	A549	lung:	n/a
15	chr3:195717366-195717416	MCF-7	breast:	n/a
16	chr3:195701118-195701168	HCF	heart:	n/a
17	chr3:195678176-195678226	HEEpiC	esophagus:	n/a
18	chr3:195717416-195717466	HepG2	liver:	n/a
19	chr3:195678176-195678226	AG04450	lung:	fetal
20	chr3:195700735-195700785	AG09309	skin:	n/a
21	chr3:195687741-195687791	HNPCEpiC	eye:	n/a
22	chr3:195714100-195714150	HEK293	kidney:	embryo
23	chr3:195719790-195719840	NHDF-neo	bronchial:	n/a
24	chr3:195678176-195678226	HCT-116	colon:	n/a
25	chr3:195717344-195717394	SAEC	small airway:	n/a
26	chr3:195716632-195716682	GM06990	blood:	n/a
27	chr3:195717366-195717416	Jurkat	blood:	n/a
28	chr3:195716626-195716676	LNCaP	prostate:	n/a
29	chr3:195687741-195687791	AG04450	lung:	fetal
30	chr3:195682326-195682376	NHBE	bronchial:	n/a
31	chr3:195681400-195681450	NHBE	bronchial:	n/a
32	chr3:195723614-195723664	SK-N-MC	brain:	n/a
33	chr3:195709698-195709748	HCF	heart:	n/a
34	chr3:195717574-195717624	Hela-S3	cervix:	n/a
35	chr3:195688021-195688071	HRE	kidney:	n/a
36	chr3:195717574-195717624	AG09319	gingival:	n/a
37	chr3:195714100-195714150	ovcar-3	ovarian:	n/a
38	chr3:195716626-195716676	HRPEpiC	eye:	n/a
39	chr3:195717574-195717624	HEK293	kidney:	embryo
40	chr3:195678176-195678226	A549	lung:	n/a
41	chr3:195716626-195716676	PFSK-1	brain:	n/a
42	chr3:195709661-195709711	RPTEC	kidney:	n/a
43	chr3:195678176-195678226	GM12891	blood:	n/a
44	chr3:195709698-195709748	IMR90	lung:	fetal
45	chr3:195709661-195709711	AoSMC	blood vessel:	n/a
46	chr3:195717574-195717624	AG10803	skin:	n/a
47	chr3:195717574-195717624	RPTEC	kidney:	n/a
48	chr3:195700735-195700785	HCPEpiC	choroid plexus:	n/a
49	chr3:195683635-195683685	U87	brain:	n/a
50	chr3:195709698-195709748	HEK293	kidney:	embryo

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195361738..195362245-chr3:195681393..195681916,2	HCT-116	colon:
2	chr3:195639677..195641924-chr3:195679365..195681428,2	MCF-7	breast:
3	chr3:195419233..195421889-chr3:195682348..195684419,2	K562	blood:
4	chr3:195384346..195385021-chr3:195716746..195717598,2	HCT-116	colon:
5	chr3:195620748..195623057-chr3:195678515..195681386,2	K562	blood:
6	chr3:195620748..195623055-chr3:195679886..195681403,2	K562	blood:
7	chr3:195679870..195682569-chr3:197379763..197382610,2	K562	blood:
8	chr3:195586120..195586802-chr3:195721315..195721912,2	MCF-7	breast:
9	chr3:195645901..195648267-chr3:195679890..195681479,3	MCF-7	breast:
10	chr3:195679874..195682569-chr3:197381110..197382679,2	K562	blood:
11	chr3:195636473..195638760-chr3:195679951..195681488,2	MCF-7	breast:
12	chr3:195673861..195675995-chr5:278201..279705,3	K562	blood:
13	chr3:195361732..195362263-chr3:195681373..195681896,2	MCF-7	breast:
14	chr3:195416074..195419636-chr3:195682871..195685500,3	K562	blood:
15	chr3:195384344..195385079-chr3:195717098..195717747,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-2	chr3:195665538-195665609	NONHSAT094271
2	lnc-TFRC-1	chr3:195666277-195666553	NONHSAT094273
3	lnc-TFRC-1	chr3:195668449-195672581	NONHSAT094272
4	lnc-TNK2-6	chr3:195688656-195689069	expReg_chr3_13675_-
5	lnc-TFRC-1	chr3:195666274-195667064	NONHSAT094272
6	lnc-TNK2-2	chr3:195676059-195679566	ENSG00000260261.1
7	lnc-TNK2-2	chr3:195674206-195674576	NONHSAT094271
8	lnc-TNK2-2	chr3:195673684-195674350	NONHSAT094275
9	lnc-MUC20-9	chr3:195674996-195675559	NONHSAT094276
10	lnc-TNK2-2	chr3:195676113-195676284	NONHSAT094275

No data

Variant related genes	Relation type
SDHAP1	TF binding region
ENSG00000231464	TF binding region
ENSG00000260261	TF binding region
SDHAP1	CpG island
ENSG00000231464	CpG island
ENSG00000260261	CpG island
ENSG00000061938	chromatin interactions
ENSG00000215837	chromatin interactions
ENSG00000242086	chromatin interactions
ENSG00000229178	chromatin interactions
ENSG00000266730	chromatin interactions
ENSG00000273009	chromatin interactions

Extended variants
information (count: 3285 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3285 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549940801	chr3:195664626-195664627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568311621	chr3:195664633-195664634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139426184	chr3:195664645-195664646	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
4	rs550151113	chr3:195664667-195664668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371845347	chr3:195664668-195664669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553386697	chr3:195664671-195664672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571673607	chr3:195664695-195664696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539148626	chr3:195664701-195664702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371331462	chr3:195664744-195664745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557527503	chr3:195664792-195664793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576076437	chr3:195664811-195664812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145678023	chr3:195664813-195664814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562284786	chr3:195664839-195664840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370196054	chr3:195664863-195664864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574418279	chr3:195664871-195664872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113065615	chr3:195664872-195664873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367703027	chr3:195664897-195664898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371263872	chr3:195664906-195664907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575312	chr3:195664955-195664956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397833930	chr3:195664958-195664959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113034267	chr3:195664971-195664972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201431379	chr3:195664977-195664978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114300408	chr3:195664987-195664988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138074429	chr3:195664993-195664994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551865237	chr3:195665001-195665002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149888231	chr3:195665024-195665025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191274730	chr3:195665030-195665031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531033685	chr3:195665031-195665032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549739721	chr3:195665037-195665038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149466438	chr3:195665039-195665040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147144104	chr3:195665052-195665053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547261563	chr3:195665084-195665085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140268413	chr3:195665092-195665093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11708303	chr3:195665099-195665100	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs147367973	chr3:195665110-195665111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114774926	chr3:195665115-195665116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537132046	chr3:195665120-195665121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375124182	chr3:195665135-195665136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11705807	chr3:195665137-195665138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs574254604	chr3:195665138-195665139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183996781	chr3:195665139-195665140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188389638	chr3:195665141-195665142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578248149	chr3:195665175-195665176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201315852	chr3:195665209-195665210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545121021	chr3:195665223-195665224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199972692	chr3:195665252-195665253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563679423	chr3:195665279-195665280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530942937	chr3:195665301-195665302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543073445	chr3:195665302-195665303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561569292	chr3:195665314-195665315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2070 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195647200-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:195648600-195666600	Weak transcription	Lung	lung
3	chr3:195648600-195666600	Weak transcription	Spleen	Spleen
4	chr3:195648600-195680600	Weak transcription	Pancreas	Pancrea
5	chr3:195648800-195666600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr3:195648800-195666800	Weak transcription	Esophagus	oesophagus
7	chr3:195651200-195671200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:195651800-195673800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:195653000-195666800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr3:195656600-195681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:195656800-195666600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:195656800-195666600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr3:195656800-195669200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:195656800-195671200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr3:195656800-195676400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr3:195656800-195679400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr3:195657000-195666800	Weak transcription	Primary T cells from cord blood	blood
18	chr3:195657200-195666800	Weak transcription	Thymus	Thymus
19	chr3:195657400-195670000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:195657800-195681400	Weak transcription	GM12878-XiMat	blood
21	chr3:195658400-195666800	Weak transcription	Gastric	stomach
22	chr3:195658800-195666800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr3:195659000-195667200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:195659000-195676400	Weak transcription	Hela-S3	cervix
25	chr3:195659600-195666600	Weak transcription	Brain Anterior Caudate	brain
26	chr3:195659600-195666800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:195659600-195681200	Weak transcription	Brain Hippocampus Middle	brain
28	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
29	chr3:195660000-195666600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:195660000-195666600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:195660000-195666600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr3:195660000-195666600	Weak transcription	Fetal Muscle Leg	muscle
33	chr3:195660000-195666800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:195660000-195666800	Weak transcription	Brain Substantia Nigra	brain
35	chr3:195660000-195666800	Weak transcription	Fetal Intestine Large	intestine
36	chr3:195660000-195666800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr3:195660000-195669800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr3:195660000-195681200	Weak transcription	Colonic Mucosa	Colon
39	chr3:195660200-195666600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:195660400-195666600	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr3:195660400-195666800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr3:195660400-195666800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr3:195660400-195680600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr3:195660600-195666400	Weak transcription	Fetal Intestine Small	intestine
45	chr3:195660600-195666800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr3:195660600-195669600	Weak transcription	A549	lung
47	chr3:195660600-195681200	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr3:195660800-195666800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr3:195660800-195667000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:195660800-195669400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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