EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS007-05528 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr15:40390020-40391850 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF13MA0657.1chr15:40390335-40390353TGGCCACGCCCATTGCTT+6.1
Klf12MA0742.1chr15:40390336-40390351GGCCACGCCCATTGC+6.33
SP1MA0079.4chr15:40390334-40390349ATGGCCACGCCCATT+6.37
SP3MA0746.2chr15:40390336-40390349GGCCACGCCCATT+6.07
SP4MA0685.1chr15:40390334-40390351ATGGCCACGCCCATTGC+6.2
ZNF263MA0528.1chr15:40390649-40390670AAAGAAGGGAGAGGGAGGGGG+6.21
ZNF263MA0528.1chr15:40390930-40390951TCTCCCTTAGTCCCCTCCTCC-6.33
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_02129chr15:40389203-40391981Aorta
SE_09809chr15:40384570-40394646CD14
SE_10247chr15:40384267-40394494CD19_Primary
SE_10901chr15:40379120-40402300CD20
SE_24160chr15:40389836-40391582Colon_Crypt_2
SE_28229chr15:40389267-40392754Fetal_Intestine
SE_29542chr15:40388382-40392097Fetal_Intestine_Large
SE_30713chr15:40389612-40391988Fetal_Muscle
SE_30953chr15:40387576-40392857Fetal_Thymus
SE_31657chr15:40389583-40391858Gastric
SE_32631chr15:40385680-40400407GM12878
SE_33749chr15:40383375-40394469H2171
SE_37146chr15:40389411-40393555HSMMtube
SE_41090chr15:40389574-40391921Left_Ventricle
SE_41752chr15:40389435-40391543LNCaP
SE_42538chr15:40389475-40391985Lung
SE_43725chr15:40386787-40394532MM1S
SE_46900chr15:40389894-40391600Ovary
SE_47647chr15:40389842-40391652Pancreas
SE_49093chr15:40389600-40391822Right_Atrium
SE_50219chr15:40388963-40391821Sigmoid_Colon
SE_51397chr15:40389521-40401944Skeletal_Muscle
SE_52941chr15:40389709-40391796Small_Intestine
SE_54376chr15:40389572-40391790Spleen
SE_58347chr15:40336303-40409644Ly1
SE_58853chr15:40336022-40409018Ly3
SE_59746chr15:40336643-40415102Ly4
SE_60404chr15:40336144-40409045DHL6
SE_61090chr15:40336308-40414973HBL1
SE_61688chr15:40336793-40410942Toledo
SE_62368chr15:40336601-40408809Tonsil
SE_65648chr15:40389445-40391908Pancreatic_islets
SE_67334chr15:40386787-40394532MM1S
SE_68227chr15:40361115-40402006TC32
SE_68538chr15:40360882-40401938TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr154039022040390395
chr154039103240391342
Enhancer Sequence
CAGGGCCGGC CTGGGGAGCA CCATCTTCCC GGCAGACTCA CGAAATCCCT GGGAGATCCC 60
TGACTTTCTG CTTTGAGACT GCCCACAGCA GCCACAGGCC ATGGGGCTCA GGATTCTAGG 120
CTGCCAGGGT AAGCCAAGGA TTCTGAAACC CAGAGGGCAA CCCCTTGGAC CCAGTGGGCC 180
CACTGCCTCA GACTGCTTCT GACCCAGAGG CCCGAGGAAC GAGCAACGTG GCAAAACGGA 240
AAAGGAAAAA AAAGACTCCT TGCCAAGAGC TTCCTCAGCC CAGCCAGCAG TGTTAACAGG 300
ACATTGAAGC CACCATGGCC ACGCCCATTG CTTCTCTAAG GAAAAAAGAG CAGTCCGAAG 360
CCAGCCAGCT CTCAGTGGAA GATGGCAAGG CTTCCTCTAA CGCAACTGGA AGACACTGGC 420
TCCAGCCACT GGGGGTTGAG GGGTACGGTT CGGGGACAGA GCTGTGCTGC ACCATCCATG 480
TCCCCAGACC CTTGTTTTGC ACCTCCACAG CCTGGAGGGA GGAACTACTG AGACCCTTAC 540
TCAGTTTCCT TCAAGCTGAG AACAGCTCCA TCAAACTACT GGGCAACTTC TTCAGAGCTC 600
AGAAGGGCAC AATGGTGTGT GCCCTGGTTA AAGAAGGGAG AGGGAGGGGG TTCGGGGGAC 660
AAGCCTGTTG TGTGTATTAT GCTATGCAAA ATAACCCCAG GTTCTGACAC TCGACTTGGG 720
GTCTTTTCAG CTGACTGTTC ATGTCCTGTC CAGGACCAGG TCAAGGCAAA CCAGGCAAGG 780
AGGAAGGATG GAACCCTCCC CTTCACACAC GGACTGATTG TGTGCTCTGG TCATGGAACA 840
TGACCTCTTG GCTGCCAGAC ATGGATCAAA AGGCAAACCA GTCATTTTTC TTTAACCTTC 900
TTTCTTTGTG TCTCCCTTAG TCCCCTCCTC CCATCACCCA CTTTCCAAAA AAAAAAGCCA 960
ATTTCCATCC CATGGCAGGC CTTGGTGGGG AGGGAATGAA CTCTCCGGAA CTACAAGGCC 1020
CTTCTCCTGG AAGAGAGAGC AGTCAGGTGC AGAGTGTGTG GGGAACTCAG CCTCTAGTCT 1080
GCCACGCTGA TGACTCAGAA GCTAAATATA GCGAGCGATA TAAACAGAGC CAGCCACAGA 1140
GCAAACACAG GGCCCCCAGC CCCGGCGCTG GCTCTCACGC ACTCTGGCTC TCCGCAGTCC 1200
CTCCCCCAGC CTCATTCTTC CCCTGGCACT GTCCTAGGTG GGCCTCCCAC TCCTGGGACA 1260
GAGGCTGGCT TCCTAGGGAC CCATCTCACT CTATAGCAAA CCTCTGGGGC CCCTGCCCGG 1320
GGCTGTCCCA TCTAGACGCT GAGCAACCTA GTTAGCCAGC TTAAGTTCCA GAAAACCACT 1380
CACTAATAAC TAGAGAATCC CAAAGTGTCA GGAAGCAATC AGGGGCTCCC TGAACAAAGG 1440
ATCCAGTCTG CTAGGCAGAG AAGCTGCTAG TTAATAAACC ATGCAAACAC CAACTCGGGT 1500
ACAACTTCCA AAAGAGCTCC CCAAATTACA AAGTCAGGTC CAAGCAAAAT CCTAAAGTCA 1560
TCTTTTAACA TATTTCTAAA AGTACTCAAC TGTCCCTGAC TTAATAGTTA TTTGTATCAC 1620
AACTCCTAAA GGCCCTTCAC ATCAACTAGG CAAGGTAAGT ATTAGAAACC AAGACTAAGC 1680
CGGGTGCAGT GGCTCACACC TGTAATCCCA GCACTTTGGG AGGCCGAGAT GGGCGGATCG 1740
CCTGAGGTCG CGAGTTCAAG ACAAGCCTGA CCGACATGGA GAAACCCCGT CTCTACTAAA 1800
AATACAAAAA TTAGCCAGGC ATGGTGGTGC 1830