EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-04640 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr10:104379310-104381980 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MafbMA0117.2chr10:104379450-104379462AGTCAGCACTTT-6.32
RARA(var.2)MA0730.1chr10:104380634-104380651CGGTCACATAGGGGTCA+6.14
Tcf12MA0521.1chr10:104380796-104380807CAGCAGCTGTT-6.32
ZNF263MA0528.1chr10:104381471-104381492GGAGGAAAGGGAGGGAAAAGA+6.18
ZNF263MA0528.1chr10:104381376-104381397TTCCCCGTCCCTGCCTCCTCC-6.72
ZNF263MA0528.1chr10:104381468-104381489AGAGGAGGAAAGGGAGGGAAA+7.76
ZfxMA0146.2chr10:104379994-104380008CCAGCCCAGGCCTG+6.19
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00121chr10:104378915-104383644Adipose_Nuclei
SE_01828chr10:104379235-104382190Aorta
SE_03401chr10:104379384-104380018Brain_Angular_Gyrus
SE_03401chr10:104381210-104382038Brain_Angular_Gyrus
SE_03928chr10:104379021-104382268Brain_Anterior_Caudate
SE_04957chr10:104379199-104382450Brain_Cingulate_Gyrus
SE_05850chr10:104378799-104382498Brain_Hippocampus_Middle
SE_06794chr10:104379144-104382330Brain_Hippocampus_Middle_150
SE_07900chr10:104379407-104382399Brain_Inferior_Temporal_Lobe
SE_26660chr10:104378442-104380460Esophagus
SE_26660chr10:104380530-104382050Esophagus
SE_28107chr10:104379124-104381031Fetal_Intestine
SE_29332chr10:104379246-104380989Fetal_Intestine_Large
SE_29601chr10:104378929-104382213Fetal_Muscle
SE_31097chr10:104381132-104382028Fetal_Thymus
SE_31421chr10:104380547-104382233Gastric
SE_36963chr10:104378298-104383584HSMMtube
SE_38034chr10:104379321-104382171HUVEC
SE_40696chr10:104378395-104382037Left_Ventricle
SE_42120chr10:104378392-104382398Lung
SE_44897chr10:104380869-104381457NHLF
SE_44897chr10:104381536-104382064NHLF
SE_46355chr10:104378421-104382236Osteoblasts
SE_46884chr10:104380040-104380477Ovary
SE_48263chr10:104378356-104380349Psoas_Muscle
SE_48604chr10:104378421-104382171Right_Atrium
SE_50092chr10:104379510-104382162Sigmoid_Colon
SE_51270chr10:104374691-104382277Skeletal_Muscle
SE_52411chr10:104379172-104381814Small_Intestine
SE_53301chr10:104379581-104382177Spleen
SE_54642chr10:104376854-104382249Stomach_Smooth_Muscle
SE_55138chr10:104381175-104381597Thymus
SE_62334chr10:104369841-104439105Tonsil
SE_63929chr10:104379015-104382372HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10104380200104381891
Number: 1             
IDChromosomeStartEnd
GH10I102618chr10104378483104382239
Enhancer Sequence
CCCCAAGCAC CCACCCTTGA TCACCGAGGG GTTTCTCAGG CCCTTTCCAA GGAGCCCTGG 60
GAAACCCTCT GACCCTGCCC CCAGCCGGAT TCTCAGCAGT GGAGCCAACA CCCACACCAG 120
CCCTCCTCCC CCTGCCAGGC AGTCAGCACT TTCTCCCTCT GACTGCCAGC CAGCCGCCCC 180
TGTTAGGGTC CTGCCACTGT GGTCACAGGC AGCTCCCTTG CTTGTGGGAA CCTGGGCTTG 240
TAATTACTTG TGGGCCTCTA GATCTCCCTC TGGGGCTGGC TGTCTCCCTG GGAGTCTGCA 300
GGACCTCCTA GAGGCCTGGG GTTAGACTTG CAGTCGCCAG TGAGGGCCAC TCCACTGGGC 360
CAAGGAGAGC CATAGGTCCC TCAGGAGGGG ACCCCAGCAC AAAGAGGCCC ACCCTTGCTC 420
CCTGCAGGCA TCTCTTGCTC GCACCCCCAG GGTTCCGAGG TGTCTTCTTG GGCCTTGTGT 480
GCCCAGGCCT ATTGGAGGCA GAGGAGTAGG AAGGAGTGAA ATCCAATAGA CCCAGGACAT 540
GACGAGACCC AGTCTTATGT TCTCTTAACT GCTGCCGGAA CTCTCCCATT GGTCCCAGCT 600
GAAATGGAGG GGCTGGGATG ACTTTGTTAC AGCAGCCTTG GAAGCCCTCA CTCCCAGCCT 660
TGGCACCTTG TTCTGGCCAC CAGCCCAGCC CAGGCCTGTT ATCTCTTGGG AGAAAGCGTG 720
GCAGAGACAT CCTGCAGGGG GAAGAGTGAC AAGGAGAGGC CGAGAGGAAA AGGCAGAAGG 780
TTTAGGAACC CGAGCCCCTT TCCGGAGCCT GTGGAATGGC CCCAGACAGG CCTCCACACC 840
CACCTGCTCC ACAGCCTTCC CCCATCAGTC CAGACCCAGG AGAGTCAGGG CCCCAGCATG 900
TGGCAAAGCA GGGCTTGTCT GCAGCACCAG GTGGAGCACA GTGGACACTC CCTGCTTTAT 960
GGAGGATCTG GGGGTGCAGG AAGCCAGCTC CAGTTCCACA GGCTTTCACT TTCTGGAGAA 1020
CAGCACCTTG ACTCCGTCTG CCCTGCCATT TGCTGTTTTC ATCCTTGCTG AGACTGTAAA 1080
GCTTATCAGC CAATTCCGGG GCTGTGCAGG AGGCTCTTCA GACCCTGGGA GGGGGCCTGC 1140
CAAGGTCTGC TCCTGCACCT CCTTCCCCCA GCATTCCTCA TCCTGGTGGC TTTAACAAGC 1200
CTCTCTCCCT TGAGCCTGTC AACACTGGGC TGTTAGTCTT CTGAGCGGGA GCCCGGCCCA 1260
GAGCTGAGTT GTTCATCCGT CCCCAGCCAG GGTTGATCTG AAGGGGGATA AGTCTCAGCC 1320
CCAGCGGTCA CATAGGGGTC ACATCACCAA ATATGAGAAT ATTGTTTTAG GCCCCGCAAT 1380
GCTTTCTCAG CTGTGTGGTG TCTGACAGCT CACCCAGGTT GCGCCCCTAG TCCCAGCCAT 1440
TCTCTGCCAG TCCTGATGGG AAGCCCCAGG CGTGGGAGAA GACGCCCAGC AGCTGTTCCA 1500
AGTGGGCTCT GCTGCTCCAG GCCAGGCTTG GGAAGGTGCT GCCGAGCTCT CCTCTGGGCA 1560
AGCCCTGCCT TCTGCTACCC ATTTGGATAT TGTGTAGAAG ATGACTTGGG AATCCCCAGC 1620
CCATGCCCTG GGCACCTCCT CTTTGGTGCC TCTACTGTTC CTCCTTCCAC GGGTGAACCC 1680
AGGCATACTT ATTCTCCCTG GAGACCTTTG CTTGGACTGC CCCGAGACCT TGTTGTCCAG 1740
GGGGACACCC ATTAAGGTTT AGAGCCCAGC AATGCGCCTG GGGAAGTACC CTCCCTTGTA 1800
GGAAAGGACT GTGATGCCGC CCTGTGTCCC TGGCAGCCCA CAGCCAGAGC AGGAGTCTGA 1860
GCCCGCTTCT GGCCACCAGA GCCAACTTTT CACCGCCCAC TAAGAACAGG AAATGAGCGA 1920
GACCTGTGCC CCAACTGCAG CCCGCTACCT GCCGCACCAC ACGCCTCTGT CCCTGACCTG 1980
GGTTGGGGGT GTTCTCCAGG CTGTTTTCTG GCTTTTGTCT GGCCTGTGGA GTGGGGGTGG 2040
GAGGGAAGGG ATGCAGACAG GACTGCTTCC CCGTCCCTGC CTCCTCCACT GCCATCGTGG 2100
GTGCCAGAGC AGCTCCTTGG CAGGCTCTTC CACTGTAAAC AACACATTTC CTTCCCTGAG 2160
AGGAGGAAAG GGAGGGAAAA GAAAGCCAAA TTTGTTGGGA AGCAAGTACA ACGTGTCAAC 2220
ATGAAGAACA AACAATGCCC TGGACAAAGT GTGGATTGTC ATACCAAAGG GAAGGAGTGG 2280
GCATTGTCAG CCACTCTTTG CAGACTCAGA AATATCATTG ACCACAGACA TCTGAATCGG 2340
CGTCAGATCT GCAGCAGCTG GGCCCCTGCC TGCAGTGCAG CCTGGCTTGC CCAGGGCAGG 2400
CACTGACACA AGATCACTTT TCGGGTTCCT TTCTGGAACT TGCTGGGGCC TGGGGAATTG 2460
GGAGGTTGTT GACAGTCCTC CCTCACCACC ACCCAGCCAA GCTGGTTAAG GCAGCTGGTG 2520
TGAGCCCACT GGAGTAGCTG CTGGCCTAGA TTCCAAGCCC CCCTCCCTGG CCAAAGGTGG 2580
GAACTGGGGG TAACCAAGAT CCATTGCCCC CCTCGCAGCT CAGCCCGTTT GATGGTGGTG 2640
AAGCTACAGC CACCAACTCA CCCCTGTTGG 2670