EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-11907 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr14:77427170-77429310 
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
TGCTGGAATT ACAGGCGTGA GCCACCACGC CCAGCCAGAA TTTTTTTTAA AAAAAGGAAA 60
TAGAAGAGAA TGTAAGAATA GAAGTGCAGG TTAAAAGGAA CGTTTAATTT CATAAAGTTT 120
TTGCCTCAGG GTAGTATGCT TGTCTGAGTA ATGGGTTGAG ATAGGAACGC ATTTCTTAGT 180
GCAGGTCTTG ATTTCAAATG TTCGAAAGCC ACTGCTCTGG AAAATAGAGG AGTGGAGACC 240
AAAGTGTGCC CTTTGTGTAT GTGTCGGCAG TGGGGTGGGG GTGGGGGTCT CTGTCCTAGC 300
ATTTGGTTGC AGCACCCCAG GAGTGCCTGT AGGGGAACCA CTGACCTCCA CTTTTCCATA 360
CGCTTCACAC CTTCACACCG AAATGTGCTC CATTCCCTTT GCTATTTTTT TTTCTTTTCT 420
TTTTTTTTTT TTTAGACAGA GTCTAGCTCT GTCGCCCAGG CTGAAGTGCA GTGGCACGAT 480
CTCGGCTCAC TACAACCTCT GCCTCCTGGG TTCGAGTGAT TCTCCTGTCT CAGCTTCCTG 540
AGTAGCTGAG ACTATGCCTG GCTAACTTTT GCAGTTTTAG TAGAGACGGG GTTTCACCAT 600
GTTGGCCAGG CTGGTCTCAA ACTCCTGACC TTAGGTGACC TGCCCACTTC AGCCTCCCAA 660
AGTGCTGGGA TTACAGGCGT GAGCCACCTC ACCCAGCCTG CTATTTTCAT TAGGAGGAAA 720
AGAGGGATGG TAGCTTTCAT CCAGATCCCC CATCTTCAGA ATGTTTTCAA CTTTCCCCAG 780
AACCTCCACA GCGTTAAGTC AGTCAAAATC CTTGGATGGA CCCTTCCAAG TAGCAAGGGC 840
CACCCTGTCC CCTTTCCCCT GGCCATGAGA CCACGCAGAG CGCAGGGGCC GGAGTCAGAA 900
AGGGCAGTTT GGCCCCTGGG CAGTCTCCTG AGAGTCTTTC TCCTCCCAGT TTCTACTATT 960
TGGCGGAACC TTGAATGCAG GGGGGCGGGA CAGAGAAAAA ACTAGAAAGC TCGACTTCTG 1020
CCTGCGGGGC CGGAAGCCCC GCTGCGGCCC CAGCCCGCGG TTAGCCCCTG TTTGTCATTT 1080
TGCAAATCTG GTCAACCCAC CTCCGGTGAA AACTCCCAAC CTCACCCCAG GGGGCAATGA 1140
CTAATTACAA AACACATTTT CTCTCGTTTT CGTCAAGCTC GCTGTCCCGC CCACACATCC 1200
CCCGCCTATC CCGGCACCCG TCGGCTTCCT CAGGAGCCTC ACTCAACTGT GTTGAATGAA 1260
CTCTTGGCCT GGTCCCTCCC CCAGAGACTT CACACCGTGG GGTTCTTTCC TCCCTGCTCA 1320
GCTTTACTTT CACTTTCTAG TCACTCTCAC TTCTCTGTCA GCTTCAGCTT CTCACCCTAG 1380
AGCTTGAGCC CTGGTCCTTT CTTAAGGCAG GGGCTATTGC CCAAGTCCTG GGCTGCACCC 1440
AATTCGTCAA AAGTCTCGAT TCATCAATAG TCAAAAATAT TTATCAAATG CATTCTGTTC 1500
CAGGCTCTAG GAATGCAGTG CAAGACAGGC AAGGTTCTTG CTCATACAGA GCTTCTAGAA 1560
ACCTGGGATA CAGAGATGCA ATCAAGTGAT AAAACACATG GATGAAGGCT CTGCCATTGA 1620
ACACATGGTT CTTGACAAGC CCACAGAGAG GCACAGCTAA GCCAGCCCTG GGGAGCCAGG 1680
GAGGGTTCCC TGGAGGGAGA GAAGCTGGAT CCAGGTCTGA AAGATGACTT GAAGTCAGCC 1740
ATGAGCAAGG AAGAGATTTT CCAGGCCAAG CGAACAGCCT GTGAGTGGTG CCATTTGGGT 1800
GAGGCTGGCT GGAGCTCACA GGGTGGGAGG GAGTGCAGGG AGCTGGGGTC CCCAAAGGTG 1860
GAAAGAAGCC AGACCCAAAA GGACTTTGAA ATTCTGCTCA GCCATTTGGA TTTTGTCCTG 1920
AGGGTGATGG AGATTTGTGA GCCCCAAATA TCTGAGACAG GTCCCAGTCC CTTTAGAAAG 1980
TTTATTTTTG CCAAGGGTAA GGACAAGCCC ATGACACAGC CTTAGGAGGT CCTGAAGACA 2040
GGTGCGCAAG GTGGTCAAGG TACAGCTTGC TTTTATACAT TTTAGGGAGA TATAATACAT 2100
CAATCAATAT ATGTAAGATT TACATGGGTT CTGGCCGGGC 2140