EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-11122 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr15:40389680-40391820 
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
CTTCCTTGTA CCCTTGTTTT CCGGAATGTG ATTGCTGGGC AGCAGGTATG GGGCGATTGG 60
ACCATGGTTC CAGAATCCAT CAAATCTGTA TGACGCCTAG CTCAGCAAAT TACGGTGTGA 120
CTTGGACATG TTACCTCACT TCTCTGAGCC TCAGTTTCCT ATAACACAGT GGCAATGGAG 180
TCTAAAAGTC CAAGGTTGCT GTGGTGATTA CGTAAGAAAA ATATACATGA AGCACTGGGC 240
CTGGGGGCTG CAAGGAGCAG GCTCCTCCTT CCCTGGGGAG CACAAGGAAA ACCTGGGACT 300
CACTGGCTTT GCAGAGCACG TCTCTCAATA TGCTCTGCAA CAGGGCCGGC CTGGGGAGCA 360
CCATCTTCCC GGCAGACTCA CGAAATCCCT GGGAGATCCC TGACTTTCTG CTTTGAGACT 420
GCCCACAGCA GCCACAGGCC ATGGGGCTCA GGATTCTAGG CTGCCAGGGT AAGCCAAGGA 480
TTCTGAAACC CAGAGGGCAA CCCCTTGGAC CCAGTGGGCC CACTGCCTCA GACTGCTTCT 540
GACCCAGAGG CCCGAGGAAC GAGCAACGTG GCAAAACGGA AAAGGAAAAA AAAGACTCCT 600
TGCCAAGAGC TTCCTCAGCC CAGCCAGCAG TGTTAACAGG ACATTGAAGC CACCATGGCC 660
ACGCCCATTG CTTCTCTAAG GAAAAAAGAG CAGTCCGAAG CCAGCCAGCT CTCAGTGGAA 720
GATGGCAAGG CTTCCTCTAA CGCAACTGGA AGACACTGGC TCCAGCCACT GGGGGTTGAG 780
GGGTACGGTT CGGGGACAGA GCTGTGCTGC ACCATCCATG TCCCCAGACC CTTGTTTTGC 840
ACCTCCACAG CCTGGAGGGA GGAACTACTG AGACCCTTAC TCAGTTTCCT TCAAGCTGAG 900
AACAGCTCCA TCAAACTACT GGGCAACTTC TTCAGAGCTC AGAAGGGCAC AATGGTGTGT 960
GCCCTGGTTA AAGAAGGGAG AGGGAGGGGG TTCGGGGGAC AAGCCTGTTG TGTGTATTAT 1020
GCTATGCAAA ATAACCCCAG GTTCTGACAC TCGACTTGGG GTCTTTTCAG CTGACTGTTC 1080
ATGTCCTGTC CAGGACCAGG TCAAGGCAAA CCAGGCAAGG AGGAAGGATG GAACCCTCCC 1140
CTTCACACAC GGACTGATTG TGTGCTCTGG TCATGGAACA TGACCTCTTG GCTGCCAGAC 1200
ATGGATCAAA AGGCAAACCA GTCATTTTTC TTTAACCTTC TTTCTTTGTG TCTCCCTTAG 1260
TCCCCTCCTC CCATCACCCA CTTTCCAAAA AAAAAAGCCA ATTTCCATCC CATGGCAGGC 1320
CTTGGTGGGG AGGGAATGAA CTCTCCGGAA CTACAAGGCC CTTCTCCTGG AAGAGAGAGC 1380
AGTCAGGTGC AGAGTGTGTG GGGAACTCAG CCTCTAGTCT GCCACGCTGA TGACTCAGAA 1440
GCTAAATATA GCGAGCGATA TAAACAGAGC CAGCCACAGA GCAAACACAG GGCCCCCAGC 1500
CCCGGCGCTG GCTCTCACGC ACTCTGGCTC TCCGCAGTCC CTCCCCCAGC CTCATTCTTC 1560
CCCTGGCACT GTCCTAGGTG GGCCTCCCAC TCCTGGGACA GAGGCTGGCT TCCTAGGGAC 1620
CCATCTCACT CTATAGCAAA CCTCTGGGGC CCCTGCCCGG GGCTGTCCCA TCTAGACGCT 1680
GAGCAACCTA GTTAGCCAGC TTAAGTTCCA GAAAACCACT CACTAATAAC TAGAGAATCC 1740
CAAAGTGTCA GGAAGCAATC AGGGGCTCCC TGAACAAAGG ATCCAGTCTG CTAGGCAGAG 1800
AAGCTGCTAG TTAATAAACC ATGCAAACAC CAACTCGGGT ACAACTTCCA AAAGAGCTCC 1860
CCAAATTACA AAGTCAGGTC CAAGCAAAAT CCTAAAGTCA TCTTTTAACA TATTTCTAAA 1920
AGTACTCAAC TGTCCCTGAC TTAATAGTTA TTTGTATCAC AACTCCTAAA GGCCCTTCAC 1980
ATCAACTAGG CAAGGTAAGT ATTAGAAACC AAGACTAAGC CGGGTGCAGT GGCTCACACC 2040
TGTAATCCCA GCACTTTGGG AGGCCGAGAT GGGCGGATCG CCTGAGGTCG CGAGTTCAAG 2100
ACAAGCCTGA CCGACATGGA GAAACCCCGT CTCTACTAAA 2140