EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-10489 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr14:77426410-77429310 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs10873298chr1477426525hg19
rs10873299chr1477426711hg19
rs8181996chr1477427469hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr14:77426891-77426903GTTTGTTTGTTT+6.32
IRF1MA0050.2chr14:77428491-77428512CTTTACTTTCACTTTCTAGTC+7.7
IRF2MA0051.1chr14:77428490-77428508GCTTTACTTTCACTTTCT-6.22
PBX1MA0070.1chr14:77429266-77429278ACATCAATCAAT+6.44
SP2MA0516.2chr14:77428148-77428165AGGGGGGCGGGACAGAG-6.28
TBX20MA0689.1chr14:77427532-77427543CTTCACACCTT-6.32
TBX21MA0690.1chr14:77427533-77427543TTCACACCTT-6.02
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_01254chr14:77427828-77429221Adrenal_Gland
SE_08284chr14:77427720-77429238Brain_Inferior_Temporal_Lobe
SE_24529chr14:77427815-77429058Colon_Crypt_2
SE_27091chr14:77426354-77429307Esophagus
SE_29618chr14:77427506-77429165Fetal_Muscle
SE_31928chr14:77426377-77426988Gastric
SE_31928chr14:77427265-77429271Gastric
SE_32994chr14:77427618-77428287H1
SE_32994chr14:77428378-77429199H1
SE_34422chr14:77418557-77429646HCT-116
SE_34742chr14:77415823-77429622HeLa
SE_37233chr14:77415973-77429404HSMMtube
SE_38430chr14:77419198-77429214HUVEC
SE_41258chr14:77419224-77429300Left_Ventricle
SE_41987chr14:77427895-77428623LNCaP
SE_42676chr14:77426329-77429253Lung
SE_44184chr14:77427235-77429338NHDF-Ad
SE_46080chr14:77427116-77429322Osteoblasts
SE_46723chr14:77427822-77428631Ovary
SE_47949chr14:77427780-77429166Pancreas
SE_48706chr14:77426330-77427111Right_Atrium
SE_48706chr14:77427612-77429247Right_Atrium
SE_49653chr14:77426516-77427100Right_Ventricle
SE_49653chr14:77427823-77428586Right_Ventricle
SE_50880chr14:77427538-77429325Sigmoid_Colon
SE_53991chr14:77427468-77429327Spleen
SE_55769chr14:77427013-77429370u87
SE_65382chr14:77427384-77429616Pancreatic_islets
SE_67544chr14:77427013-77429370u87
SE_68739chr14:77427162-77429357H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr147742739877427552
Enhancer Sequence
CGCCTGCCTC GGCCTCCCAA AGTACTGGCA TTACAGATGT GAGCCGCCTC ACCCGGCTTG 60
TATTTTGTTC TTGCAGACGA AAGCTGCCCA CCAAATATGA ACAGATAGGA ACCTCGTGAT 120
CTTTTGGGGC TGTCATCCTT CTCTCAGTCT GCCAGTAACT GGGATCCTGG CATTTATCCT 180
GGAGGTCCCT GAAGGTCCAA GAGGGAACAG AGGAAATCTG ATTGGCACAG GTGTGGTGAC 240
GTGAAGCAGG TGGTGGCTTT TAGGACTGGA GGTCTGGTGT AGGGTGTATT AGTGAGGAGA 300
ACATGGAGGG AGGAACTCAC CAGGAAAATT GCAGCCAATT TCCAGCGGTC AGGAATTGAA 360
GATCCAGCAG AGTACGGAAT CAGCTCCTCC AGAGTAGTGG GTTTTTCCAG TTGTAGGTTG 420
AGATCCATTC GTGGGTCATG AAATCAAGTT AAGGGATCAT AGTCATACAC AGAATTTTTT 480
TGTTTGTTTG TTTTTGAGAC AGTCTCATTC TGTCCAGGCT AGAGTCTCTA GTCTCTGCCC 540
AGGCTAGAGT GCAGTTTCAC AGTCTTGGCT CACTGACCTC CACCTCCTGG GTTCAAGTGA 600
TTCTCCAGCC TCAGCCTCTC AAGTAGTTGG CGTTACAGGC ACCTGCCACC ACATCTGGCT 660
AATTTTTTGT ATTTTTAGTA GAGACGGGGT TTTGCCATGT TGGCCAGGCT GGTCTCGAAC 720
TCCTGGCCTC AAGTGATCCG CATGCCTTGG CCTCCCAGAG TGCTGGAATT ACAGGCGTGA 780
GCCACCACGC CCAGCCAGAA TTTTTTTTAA AAAAAGGAAA TAGAAGAGAA TGTAAGAATA 840
GAAGTGCAGG TTAAAAGGAA CGTTTAATTT CATAAAGTTT TTGCCTCAGG GTAGTATGCT 900
TGTCTGAGTA ATGGGTTGAG ATAGGAACGC ATTTCTTAGT GCAGGTCTTG ATTTCAAATG 960
TTCGAAAGCC ACTGCTCTGG AAAATAGAGG AGTGGAGACC AAAGTGTGCC CTTTGTGTAT 1020
GTGTCGGCAG TGGGGTGGGG GTGGGGGTCT CTGTCCTAGC ATTTGGTTGC AGCACCCCAG 1080
GAGTGCCTGT AGGGGAACCA CTGACCTCCA CTTTTCCATA CGCTTCACAC CTTCACACCG 1140
AAATGTGCTC CATTCCCTTT GCTATTTTTT TTTCTTTTCT TTTTTTTTTT TTTAGACAGA 1200
GTCTAGCTCT GTCGCCCAGG CTGAAGTGCA GTGGCACGAT CTCGGCTCAC TACAACCTCT 1260
GCCTCCTGGG TTCGAGTGAT TCTCCTGTCT CAGCTTCCTG AGTAGCTGAG ACTATGCCTG 1320
GCTAACTTTT GCAGTTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCAGG CTGGTCTCAA 1380
ACTCCTGACC TTAGGTGACC TGCCCACTTC AGCCTCCCAA AGTGCTGGGA TTACAGGCGT 1440
GAGCCACCTC ACCCAGCCTG CTATTTTCAT TAGGAGGAAA AGAGGGATGG TAGCTTTCAT 1500
CCAGATCCCC CATCTTCAGA ATGTTTTCAA CTTTCCCCAG AACCTCCACA GCGTTAAGTC 1560
AGTCAAAATC CTTGGATGGA CCCTTCCAAG TAGCAAGGGC CACCCTGTCC CCTTTCCCCT 1620
GGCCATGAGA CCACGCAGAG CGCAGGGGCC GGAGTCAGAA AGGGCAGTTT GGCCCCTGGG 1680
CAGTCTCCTG AGAGTCTTTC TCCTCCCAGT TTCTACTATT TGGCGGAACC TTGAATGCAG 1740
GGGGGCGGGA CAGAGAAAAA ACTAGAAAGC TCGACTTCTG CCTGCGGGGC CGGAAGCCCC 1800
GCTGCGGCCC CAGCCCGCGG TTAGCCCCTG TTTGTCATTT TGCAAATCTG GTCAACCCAC 1860
CTCCGGTGAA AACTCCCAAC CTCACCCCAG GGGGCAATGA CTAATTACAA AACACATTTT 1920
CTCTCGTTTT CGTCAAGCTC GCTGTCCCGC CCACACATCC CCCGCCTATC CCGGCACCCG 1980
TCGGCTTCCT CAGGAGCCTC ACTCAACTGT GTTGAATGAA CTCTTGGCCT GGTCCCTCCC 2040
CCAGAGACTT CACACCGTGG GGTTCTTTCC TCCCTGCTCA GCTTTACTTT CACTTTCTAG 2100
TCACTCTCAC TTCTCTGTCA GCTTCAGCTT CTCACCCTAG AGCTTGAGCC CTGGTCCTTT 2160
CTTAAGGCAG GGGCTATTGC CCAAGTCCTG GGCTGCACCC AATTCGTCAA AAGTCTCGAT 2220
TCATCAATAG TCAAAAATAT TTATCAAATG CATTCTGTTC CAGGCTCTAG GAATGCAGTG 2280
CAAGACAGGC AAGGTTCTTG CTCATACAGA GCTTCTAGAA ACCTGGGATA CAGAGATGCA 2340
ATCAAGTGAT AAAACACATG GATGAAGGCT CTGCCATTGA ACACATGGTT CTTGACAAGC 2400
CCACAGAGAG GCACAGCTAA GCCAGCCCTG GGGAGCCAGG GAGGGTTCCC TGGAGGGAGA 2460
GAAGCTGGAT CCAGGTCTGA AAGATGACTT GAAGTCAGCC ATGAGCAAGG AAGAGATTTT 2520
CCAGGCCAAG CGAACAGCCT GTGAGTGGTG CCATTTGGGT GAGGCTGGCT GGAGCTCACA 2580
GGGTGGGAGG GAGTGCAGGG AGCTGGGGTC CCCAAAGGTG GAAAGAAGCC AGACCCAAAA 2640
GGACTTTGAA ATTCTGCTCA GCCATTTGGA TTTTGTCCTG AGGGTGATGG AGATTTGTGA 2700
GCCCCAAATA TCTGAGACAG GTCCCAGTCC CTTTAGAAAG TTTATTTTTG CCAAGGGTAA 2760
GGACAAGCCC ATGACACAGC CTTAGGAGGT CCTGAAGACA GGTGCGCAAG GTGGTCAAGG 2820
TACAGCTTGC TTTTATACAT TTTAGGGAGA TATAATACAT CAATCAATAT ATGTAAGATT 2880
TACATGGGTT CTGGCCGGGC 2900