EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-08386 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr14:77427250-77429360 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs8181996chr1477427469hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
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: 27             
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_31928chr14:77427265-77429271Gastric
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_48706chr14:77427612-77429247Right_Atrium
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
GAAGTGCAGG TTAAAAGGAA CGTTTAATTT CATAAAGTTT TTGCCTCAGG GTAGTATGCT 60
TGTCTGAGTA ATGGGTTGAG ATAGGAACGC ATTTCTTAGT GCAGGTCTTG ATTTCAAATG 120
TTCGAAAGCC ACTGCTCTGG AAAATAGAGG AGTGGAGACC AAAGTGTGCC CTTTGTGTAT 180
GTGTCGGCAG TGGGGTGGGG GTGGGGGTCT CTGTCCTAGC ATTTGGTTGC AGCACCCCAG 240
GAGTGCCTGT AGGGGAACCA CTGACCTCCA CTTTTCCATA CGCTTCACAC CTTCACACCG 300
AAATGTGCTC CATTCCCTTT GCTATTTTTT TTTCTTTTCT TTTTTTTTTT TTTAGACAGA 360
GTCTAGCTCT GTCGCCCAGG CTGAAGTGCA GTGGCACGAT CTCGGCTCAC TACAACCTCT 420
GCCTCCTGGG TTCGAGTGAT TCTCCTGTCT CAGCTTCCTG AGTAGCTGAG ACTATGCCTG 480
GCTAACTTTT GCAGTTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCAGG CTGGTCTCAA 540
ACTCCTGACC TTAGGTGACC TGCCCACTTC AGCCTCCCAA AGTGCTGGGA TTACAGGCGT 600
GAGCCACCTC ACCCAGCCTG CTATTTTCAT TAGGAGGAAA AGAGGGATGG TAGCTTTCAT 660
CCAGATCCCC CATCTTCAGA ATGTTTTCAA CTTTCCCCAG AACCTCCACA GCGTTAAGTC 720
AGTCAAAATC CTTGGATGGA CCCTTCCAAG TAGCAAGGGC CACCCTGTCC CCTTTCCCCT 780
GGCCATGAGA CCACGCAGAG CGCAGGGGCC GGAGTCAGAA AGGGCAGTTT GGCCCCTGGG 840
CAGTCTCCTG AGAGTCTTTC TCCTCCCAGT TTCTACTATT TGGCGGAACC TTGAATGCAG 900
GGGGGCGGGA CAGAGAAAAA ACTAGAAAGC TCGACTTCTG CCTGCGGGGC CGGAAGCCCC 960
GCTGCGGCCC CAGCCCGCGG TTAGCCCCTG TTTGTCATTT TGCAAATCTG GTCAACCCAC 1020
CTCCGGTGAA AACTCCCAAC CTCACCCCAG GGGGCAATGA CTAATTACAA AACACATTTT 1080
CTCTCGTTTT CGTCAAGCTC GCTGTCCCGC CCACACATCC CCCGCCTATC CCGGCACCCG 1140
TCGGCTTCCT CAGGAGCCTC ACTCAACTGT GTTGAATGAA CTCTTGGCCT GGTCCCTCCC 1200
CCAGAGACTT CACACCGTGG GGTTCTTTCC TCCCTGCTCA GCTTTACTTT CACTTTCTAG 1260
TCACTCTCAC TTCTCTGTCA GCTTCAGCTT CTCACCCTAG AGCTTGAGCC CTGGTCCTTT 1320
CTTAAGGCAG GGGCTATTGC CCAAGTCCTG GGCTGCACCC AATTCGTCAA AAGTCTCGAT 1380
TCATCAATAG TCAAAAATAT TTATCAAATG CATTCTGTTC CAGGCTCTAG GAATGCAGTG 1440
CAAGACAGGC AAGGTTCTTG CTCATACAGA GCTTCTAGAA ACCTGGGATA CAGAGATGCA 1500
ATCAAGTGAT AAAACACATG GATGAAGGCT CTGCCATTGA ACACATGGTT CTTGACAAGC 1560
CCACAGAGAG GCACAGCTAA GCCAGCCCTG GGGAGCCAGG GAGGGTTCCC TGGAGGGAGA 1620
GAAGCTGGAT CCAGGTCTGA AAGATGACTT GAAGTCAGCC ATGAGCAAGG AAGAGATTTT 1680
CCAGGCCAAG CGAACAGCCT GTGAGTGGTG CCATTTGGGT GAGGCTGGCT GGAGCTCACA 1740
GGGTGGGAGG GAGTGCAGGG AGCTGGGGTC CCCAAAGGTG GAAAGAAGCC AGACCCAAAA 1800
GGACTTTGAA ATTCTGCTCA GCCATTTGGA TTTTGTCCTG AGGGTGATGG AGATTTGTGA 1860
GCCCCAAATA TCTGAGACAG GTCCCAGTCC CTTTAGAAAG TTTATTTTTG CCAAGGGTAA 1920
GGACAAGCCC ATGACACAGC CTTAGGAGGT CCTGAAGACA GGTGCGCAAG GTGGTCAAGG 1980
TACAGCTTGC TTTTATACAT TTTAGGGAGA TATAATACAT CAATCAATAT ATGTAAGATT 2040
TACATGGGTT CTGGCCGGGC GCGGTGGCTC ATGCCTGTAA TCCCAGCACT TTGGGAGGCC 2100
AAGGCAGGAG 2110