EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS095-04369 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr10:104379940-104382180 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
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: 33             
IDCoordinateTissue/cell
SE_00121chr10:104378915-104383644Adipose_Nuclei
SE_01828chr10:104379235-104382190Aorta
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
AGCAGCCTTG GAAGCCCTCA CTCCCAGCCT TGGCACCTTG TTCTGGCCAC CAGCCCAGCC 60
CAGGCCTGTT ATCTCTTGGG AGAAAGCGTG GCAGAGACAT CCTGCAGGGG GAAGAGTGAC 120
AAGGAGAGGC CGAGAGGAAA AGGCAGAAGG TTTAGGAACC CGAGCCCCTT TCCGGAGCCT 180
GTGGAATGGC CCCAGACAGG CCTCCACACC CACCTGCTCC ACAGCCTTCC CCCATCAGTC 240
CAGACCCAGG AGAGTCAGGG CCCCAGCATG TGGCAAAGCA GGGCTTGTCT GCAGCACCAG 300
GTGGAGCACA GTGGACACTC CCTGCTTTAT GGAGGATCTG GGGGTGCAGG AAGCCAGCTC 360
CAGTTCCACA GGCTTTCACT TTCTGGAGAA CAGCACCTTG ACTCCGTCTG CCCTGCCATT 420
TGCTGTTTTC ATCCTTGCTG AGACTGTAAA GCTTATCAGC CAATTCCGGG GCTGTGCAGG 480
AGGCTCTTCA GACCCTGGGA GGGGGCCTGC CAAGGTCTGC TCCTGCACCT CCTTCCCCCA 540
GCATTCCTCA TCCTGGTGGC TTTAACAAGC CTCTCTCCCT TGAGCCTGTC AACACTGGGC 600
TGTTAGTCTT CTGAGCGGGA GCCCGGCCCA GAGCTGAGTT GTTCATCCGT CCCCAGCCAG 660
GGTTGATCTG AAGGGGGATA AGTCTCAGCC CCAGCGGTCA CATAGGGGTC ACATCACCAA 720
ATATGAGAAT ATTGTTTTAG GCCCCGCAAT GCTTTCTCAG CTGTGTGGTG TCTGACAGCT 780
CACCCAGGTT GCGCCCCTAG TCCCAGCCAT TCTCTGCCAG TCCTGATGGG AAGCCCCAGG 840
CGTGGGAGAA GACGCCCAGC AGCTGTTCCA AGTGGGCTCT GCTGCTCCAG GCCAGGCTTG 900
GGAAGGTGCT GCCGAGCTCT CCTCTGGGCA AGCCCTGCCT TCTGCTACCC ATTTGGATAT 960
TGTGTAGAAG ATGACTTGGG AATCCCCAGC CCATGCCCTG GGCACCTCCT CTTTGGTGCC 1020
TCTACTGTTC CTCCTTCCAC GGGTGAACCC AGGCATACTT ATTCTCCCTG GAGACCTTTG 1080
CTTGGACTGC CCCGAGACCT TGTTGTCCAG GGGGACACCC ATTAAGGTTT AGAGCCCAGC 1140
AATGCGCCTG GGGAAGTACC CTCCCTTGTA GGAAAGGACT GTGATGCCGC CCTGTGTCCC 1200
TGGCAGCCCA CAGCCAGAGC AGGAGTCTGA GCCCGCTTCT GGCCACCAGA GCCAACTTTT 1260
CACCGCCCAC TAAGAACAGG AAATGAGCGA GACCTGTGCC CCAACTGCAG CCCGCTACCT 1320
GCCGCACCAC ACGCCTCTGT CCCTGACCTG GGTTGGGGGT GTTCTCCAGG CTGTTTTCTG 1380
GCTTTTGTCT GGCCTGTGGA GTGGGGGTGG GAGGGAAGGG ATGCAGACAG GACTGCTTCC 1440
CCGTCCCTGC CTCCTCCACT GCCATCGTGG GTGCCAGAGC AGCTCCTTGG CAGGCTCTTC 1500
CACTGTAAAC AACACATTTC CTTCCCTGAG AGGAGGAAAG GGAGGGAAAA GAAAGCCAAA 1560
TTTGTTGGGA AGCAAGTACA ACGTGTCAAC ATGAAGAACA AACAATGCCC TGGACAAAGT 1620
GTGGATTGTC ATACCAAAGG GAAGGAGTGG GCATTGTCAG CCACTCTTTG CAGACTCAGA 1680
AATATCATTG ACCACAGACA TCTGAATCGG CGTCAGATCT GCAGCAGCTG GGCCCCTGCC 1740
TGCAGTGCAG CCTGGCTTGC CCAGGGCAGG CACTGACACA AGATCACTTT TCGGGTTCCT 1800
TTCTGGAACT TGCTGGGGCC TGGGGAATTG GGAGGTTGTT GACAGTCCTC CCTCACCACC 1860
ACCCAGCCAA GCTGGTTAAG GCAGCTGGTG TGAGCCCACT GGAGTAGCTG CTGGCCTAGA 1920
TTCCAAGCCC CCCTCCCTGG CCAAAGGTGG GAACTGGGGG TAACCAAGAT CCATTGCCCC 1980
CCTCGCAGCT CAGCCCGTTT GATGGTGGTG AAGCTACAGC CACCAACTCA CCCCTGTTGG 2040
TTAAGCCTGT GCCCAAACCC CCTTTCCCTG TGGGCCTGAG TATTTCCCCA GCAGCCCCTC 2100
ACCATGATCT CCTGGGGCAC CACTTAAGAA TACAAGTGCT GGCCAGGTGC GGTGGCTCAC 2160
GCCTGTAATC AGTCCCAGCA CTTTGGGAGG CTGAGGTGGG TGGATCATCT GAGGTCGGGA 2220
GTTCGAGACC AGCCTGACCA 2240