EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS115-01401 
Organism
Homo sapiens 
Tissue/cell
Kidney_cortex 
Coordinate
chr15:40389740-40392350 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35603048chr1540391965hg19
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: 40             
IDCoordinateTissue/cell
SE_02129chr15:40389203-40391981Aorta
SE_02129chr15:40392056-40394476Aorta
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_41090chr15:40391962-40394500Left_Ventricle
SE_41752chr15:40389435-40391543LNCaP
SE_42538chr15:40389475-40391985Lung
SE_42538chr15:40392017-40402183Lung
SE_43725chr15:40386787-40394532MM1S
SE_46900chr15:40389894-40391600Ovary
SE_47647chr15:40389842-40391652Pancreas
SE_49093chr15:40389600-40391822Right_Atrium
SE_50219chr15:40388963-40391821Sigmoid_Colon
SE_50219chr15:40392076-40394462Sigmoid_Colon
SE_51397chr15:40389521-40401944Skeletal_Muscle
SE_52941chr15:40389709-40391796Small_Intestine
SE_52941chr15:40392044-40394465Small_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
ACCATGGTTC CAGAATCCAT CAAATCTGTA TGACGCCTAG CTCAGCAAAT TACGGTGTGA 60
CTTGGACATG TTACCTCACT TCTCTGAGCC TCAGTTTCCT ATAACACAGT GGCAATGGAG 120
TCTAAAAGTC CAAGGTTGCT GTGGTGATTA CGTAAGAAAA ATATACATGA AGCACTGGGC 180
CTGGGGGCTG CAAGGAGCAG GCTCCTCCTT CCCTGGGGAG CACAAGGAAA ACCTGGGACT 240
CACTGGCTTT GCAGAGCACG TCTCTCAATA TGCTCTGCAA CAGGGCCGGC CTGGGGAGCA 300
CCATCTTCCC GGCAGACTCA CGAAATCCCT GGGAGATCCC TGACTTTCTG CTTTGAGACT 360
GCCCACAGCA GCCACAGGCC ATGGGGCTCA GGATTCTAGG CTGCCAGGGT AAGCCAAGGA 420
TTCTGAAACC CAGAGGGCAA CCCCTTGGAC CCAGTGGGCC CACTGCCTCA GACTGCTTCT 480
GACCCAGAGG CCCGAGGAAC GAGCAACGTG GCAAAACGGA AAAGGAAAAA AAAGACTCCT 540
TGCCAAGAGC TTCCTCAGCC CAGCCAGCAG TGTTAACAGG ACATTGAAGC CACCATGGCC 600
ACGCCCATTG CTTCTCTAAG GAAAAAAGAG CAGTCCGAAG CCAGCCAGCT CTCAGTGGAA 660
GATGGCAAGG CTTCCTCTAA CGCAACTGGA AGACACTGGC TCCAGCCACT GGGGGTTGAG 720
GGGTACGGTT CGGGGACAGA GCTGTGCTGC ACCATCCATG TCCCCAGACC CTTGTTTTGC 780
ACCTCCACAG CCTGGAGGGA GGAACTACTG AGACCCTTAC TCAGTTTCCT TCAAGCTGAG 840
AACAGCTCCA TCAAACTACT GGGCAACTTC TTCAGAGCTC AGAAGGGCAC AATGGTGTGT 900
GCCCTGGTTA AAGAAGGGAG AGGGAGGGGG TTCGGGGGAC AAGCCTGTTG TGTGTATTAT 960
GCTATGCAAA ATAACCCCAG GTTCTGACAC TCGACTTGGG GTCTTTTCAG CTGACTGTTC 1020
ATGTCCTGTC CAGGACCAGG TCAAGGCAAA CCAGGCAAGG AGGAAGGATG GAACCCTCCC 1080
CTTCACACAC GGACTGATTG TGTGCTCTGG TCATGGAACA TGACCTCTTG GCTGCCAGAC 1140
ATGGATCAAA AGGCAAACCA GTCATTTTTC TTTAACCTTC TTTCTTTGTG TCTCCCTTAG 1200
TCCCCTCCTC CCATCACCCA CTTTCCAAAA AAAAAAGCCA ATTTCCATCC CATGGCAGGC 1260
CTTGGTGGGG AGGGAATGAA CTCTCCGGAA CTACAAGGCC CTTCTCCTGG AAGAGAGAGC 1320
AGTCAGGTGC AGAGTGTGTG GGGAACTCAG CCTCTAGTCT GCCACGCTGA TGACTCAGAA 1380
GCTAAATATA GCGAGCGATA TAAACAGAGC CAGCCACAGA GCAAACACAG GGCCCCCAGC 1440
CCCGGCGCTG GCTCTCACGC ACTCTGGCTC TCCGCAGTCC CTCCCCCAGC CTCATTCTTC 1500
CCCTGGCACT GTCCTAGGTG GGCCTCCCAC TCCTGGGACA GAGGCTGGCT TCCTAGGGAC 1560
CCATCTCACT CTATAGCAAA CCTCTGGGGC CCCTGCCCGG GGCTGTCCCA TCTAGACGCT 1620
GAGCAACCTA GTTAGCCAGC TTAAGTTCCA GAAAACCACT CACTAATAAC TAGAGAATCC 1680
CAAAGTGTCA GGAAGCAATC AGGGGCTCCC TGAACAAAGG ATCCAGTCTG CTAGGCAGAG 1740
AAGCTGCTAG TTAATAAACC ATGCAAACAC CAACTCGGGT ACAACTTCCA AAAGAGCTCC 1800
CCAAATTACA AAGTCAGGTC CAAGCAAAAT CCTAAAGTCA TCTTTTAACA TATTTCTAAA 1860
AGTACTCAAC TGTCCCTGAC TTAATAGTTA TTTGTATCAC AACTCCTAAA GGCCCTTCAC 1920
ATCAACTAGG CAAGGTAAGT ATTAGAAACC AAGACTAAGC CGGGTGCAGT GGCTCACACC 1980
TGTAATCCCA GCACTTTGGG AGGCCGAGAT GGGCGGATCG CCTGAGGTCG CGAGTTCAAG 2040
ACAAGCCTGA CCGACATGGA GAAACCCCGT CTCTACTAAA AATACAAAAA TTAGCCAGGC 2100
ATGGTGGTGC ATGCCTGTAA TTCCAGCTAC TCAGGAGGCT GAGGCAGGAC AATCACTTGA 2160
ACCCGGAGGC AGAGGTTGCA GTGAGCCGAG ATCGCACCAC TGTACTCCAG CTTGGCAAGA 2220
AGAACGAAAC GCTGTCTCAC CAAAAAAAAA AAAAAAAAAA AAAGGCTTGG AGAGATTACA 2280
TGATTTGCCC ACGAACACAT AACTTATAAG TGGCAGAGCT GGGATTTTAA CAGATCTGCC 2340
TACAAGTCTA GGATCCTTTT TGTGATATTA CAGCTAAAGA TGGTTTCAAC TGAGTGGCTG 2400
AAAGTTTTCT CAGATTTCAT TTGCCAAAAA GTCTAATTAC TATTCAGAGA TTTCCAAACC 2460
CGGCTTTTCT GAATGGAGCC ACTCCTGGTC CAAGTGAAAA AGCCATTTCC AACATGAAGA 2520
ATTCCAACCC TCCTGTAGCT TTACTCACTC GACTGTTTAC AGTAACTACT GTTTTTGAGG 2580
ATTCTTGGCT TCTTAACATT GCCCAGAAAT 2610