EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS044-04560 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr15:40390050-40391930 
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
GGCAGACTCA CGAAATCCCT GGGAGATCCC TGACTTTCTG CTTTGAGACT GCCCACAGCA 60
GCCACAGGCC ATGGGGCTCA GGATTCTAGG CTGCCAGGGT AAGCCAAGGA TTCTGAAACC 120
CAGAGGGCAA CCCCTTGGAC CCAGTGGGCC CACTGCCTCA GACTGCTTCT GACCCAGAGG 180
CCCGAGGAAC GAGCAACGTG GCAAAACGGA AAAGGAAAAA AAAGACTCCT TGCCAAGAGC 240
TTCCTCAGCC CAGCCAGCAG TGTTAACAGG ACATTGAAGC CACCATGGCC ACGCCCATTG 300
CTTCTCTAAG GAAAAAAGAG CAGTCCGAAG CCAGCCAGCT CTCAGTGGAA GATGGCAAGG 360
CTTCCTCTAA CGCAACTGGA AGACACTGGC TCCAGCCACT GGGGGTTGAG GGGTACGGTT 420
CGGGGACAGA GCTGTGCTGC ACCATCCATG TCCCCAGACC CTTGTTTTGC ACCTCCACAG 480
CCTGGAGGGA GGAACTACTG AGACCCTTAC TCAGTTTCCT TCAAGCTGAG AACAGCTCCA 540
TCAAACTACT GGGCAACTTC TTCAGAGCTC AGAAGGGCAC AATGGTGTGT GCCCTGGTTA 600
AAGAAGGGAG AGGGAGGGGG TTCGGGGGAC AAGCCTGTTG TGTGTATTAT GCTATGCAAA 660
ATAACCCCAG GTTCTGACAC TCGACTTGGG GTCTTTTCAG CTGACTGTTC ATGTCCTGTC 720
CAGGACCAGG TCAAGGCAAA CCAGGCAAGG AGGAAGGATG GAACCCTCCC CTTCACACAC 780
GGACTGATTG TGTGCTCTGG TCATGGAACA TGACCTCTTG GCTGCCAGAC ATGGATCAAA 840
AGGCAAACCA GTCATTTTTC TTTAACCTTC TTTCTTTGTG TCTCCCTTAG TCCCCTCCTC 900
CCATCACCCA CTTTCCAAAA AAAAAAGCCA ATTTCCATCC CATGGCAGGC CTTGGTGGGG 960
AGGGAATGAA CTCTCCGGAA CTACAAGGCC CTTCTCCTGG AAGAGAGAGC AGTCAGGTGC 1020
AGAGTGTGTG GGGAACTCAG CCTCTAGTCT GCCACGCTGA TGACTCAGAA GCTAAATATA 1080
GCGAGCGATA TAAACAGAGC CAGCCACAGA GCAAACACAG GGCCCCCAGC CCCGGCGCTG 1140
GCTCTCACGC ACTCTGGCTC TCCGCAGTCC CTCCCCCAGC CTCATTCTTC CCCTGGCACT 1200
GTCCTAGGTG GGCCTCCCAC TCCTGGGACA GAGGCTGGCT TCCTAGGGAC CCATCTCACT 1260
CTATAGCAAA CCTCTGGGGC CCCTGCCCGG GGCTGTCCCA TCTAGACGCT GAGCAACCTA 1320
GTTAGCCAGC TTAAGTTCCA GAAAACCACT CACTAATAAC TAGAGAATCC CAAAGTGTCA 1380
GGAAGCAATC AGGGGCTCCC TGAACAAAGG ATCCAGTCTG CTAGGCAGAG AAGCTGCTAG 1440
TTAATAAACC ATGCAAACAC CAACTCGGGT ACAACTTCCA AAAGAGCTCC CCAAATTACA 1500
AAGTCAGGTC CAAGCAAAAT CCTAAAGTCA TCTTTTAACA TATTTCTAAA AGTACTCAAC 1560
TGTCCCTGAC TTAATAGTTA TTTGTATCAC AACTCCTAAA GGCCCTTCAC ATCAACTAGG 1620
CAAGGTAAGT ATTAGAAACC AAGACTAAGC CGGGTGCAGT GGCTCACACC TGTAATCCCA 1680
GCACTTTGGG AGGCCGAGAT GGGCGGATCG CCTGAGGTCG CGAGTTCAAG ACAAGCCTGA 1740
CCGACATGGA GAAACCCCGT CTCTACTAAA AATACAAAAA TTAGCCAGGC ATGGTGGTGC 1800
ATGCCTGTAA TTCCAGCTAC TCAGGAGGCT GAGGCAGGAC AATCACTTGA ACCCGGAGGC 1860
AGAGGTTGCA GTGAGCCGAG 1880