EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS170-04032 
Organism
Homo sapiens 
Tissue/cell
RS4-11 
Coordinate
chr9:124033160-124035220 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr9:124034474-124034495CCTTCCCTCTGTCCCTCCCCT-6.09
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00021chr9:124033746-124035428Adipose_Nuclei
SE_01133chr9:124033689-124034885Adrenal_Gland
SE_01554chr9:124029611-124034978Aorta
SE_02564chr9:124033581-124035105Astrocytes
SE_02926chr9:124033924-124034926Bladder
SE_03185chr9:124030462-124035757Brain_Angular_Gyrus
SE_03897chr9:124028473-124035855Brain_Anterior_Caudate
SE_04827chr9:124028033-124035990Brain_Cingulate_Gyrus
SE_05793chr9:124026392-124035792Brain_Hippocampus_Middle
SE_06738chr9:124028205-124053307Brain_Hippocampus_Middle_150
SE_07783chr9:124027839-124053137Brain_Inferior_Temporal_Lobe
SE_08817chr9:124033874-124034298Brain_Mid_Frontal_Lobe
SE_23312chr9:124033895-124034944Colon_Crypt_1
SE_24210chr9:124034429-124034825Colon_Crypt_2
SE_25791chr9:124027829-124035823Duodenum_Smooth_Muscle
SE_26539chr9:124029120-124033538Esophagus
SE_26539chr9:124033666-124034949Esophagus
SE_26539chr9:124034970-124035708Esophagus
SE_28277chr9:124033737-124035560Fetal_Intestine
SE_29547chr9:124033793-124034795Fetal_Intestine_Large
SE_29843chr9:124033479-124035822Fetal_Muscle
SE_31451chr9:124029741-124035672Gastric
SE_37098chr9:124029141-124046023HSMMtube
SE_39048chr9:124029721-124035402IMR90
SE_40613chr9:124029047-124033462Left_Ventricle
SE_40613chr9:124033463-124035638Left_Ventricle
SE_42112chr9:124029468-124035483Lung
SE_44270chr9:124030415-124035724NHDF-Ad
SE_45112chr9:124033684-124035050NHLF
SE_46207chr9:124030373-124042994Osteoblasts
SE_46641chr9:124033852-124034360Ovary
SE_46641chr9:124034366-124034981Ovary
SE_47407chr9:124034635-124035938Panc1
SE_48576chr9:124033466-124035588Right_Atrium
SE_49531chr9:124033839-124034855Right_Ventricle
SE_50096chr9:124029101-124035800Sigmoid_Colon
SE_51483chr9:124028654-124035772Skeletal_Muscle
SE_52030chr9:124033606-124035150Skeletal_Muscle_Myoblast
SE_52458chr9:124033700-124035617Small_Intestine
SE_53608chr9:124033128-124035022Spleen
SE_54483chr9:124027675-124053334Stomach_Smooth_Muscle
SE_63851chr9:124033592-124035449HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9124034360124034626
Enhancer Sequence
CTGTGTCTGC GGCCTCTGGG TGTGTATATT TGCTTATCAG AGACCACAGG TGTGAGAGAA 60
GTTAGAAGCA CTGACTTGGA AATGGACCCC CAGTCTTGGT TCTTTGGGTG ACCTTGGGCA 120
AATCCTATCT CTCTGAGCCT CTGGTTCCTC ATGTGTAAAA TGGAGAGATG TTGGTTTGCA 180
TGATAATAAT AAAAAGCTAT CTTTTAACTG GGCATGGTGG CTCACACCTG CAGTTCCAGC 240
ATTTTGGGAG GCCGAGTTGG GTTGATGGCT TAAGCCAGGA GTTTGAGACC AGCCTGGTCA 300
ACATGGTGAA ACCCTGTCTC TACTGAAAAT ACGTGCTGGG ATGCTCCTGT AATCCTAGCT 360
ACTTGGGAGG CTGAGGTATG AGAATTGCTT AAACCCTGGA GACGGAGGTT ACAGTAAGCT 420
GAAATCACGC CACTGCACTC CAGCCTGGAT GACAGAACAA TACTGTCTCA AAACAAAAAA 480
AGAAAAGACA AAAAAAGCTA TCTTTTAATA TACCAAGCAC TGGAACATTA ATTACTTTAT 540
TGATTCCTTG CAACCATTCC TCTGAGGTAG ATACTAGTAT CTTCTTTTAC AGATGAGGAA 600
ACTGAGTCCG AGGCTGAATA ACATGCCCCG GGTTGTGTGG CTATTGGGTG ATGGTGCAAG 660
GATTCCAGAG GTCTGACGAC AGAGCCATAG CTATTAATGA CAGCACTAAA CATTCTCTTG 720
AAAATTCTTT CTAGTCCTGG TATTAGGAGA ACTGGTAAGG GAGTTTGTTA TGCTTTTATG 780
AGGGGTGGGT GTCGGTGTGC AGAGCTTGGA GAGCTCAGCC CTGCAGCAGA GAGGCCTGGA 840
GGGGCCTCCC GGGGCTGTTT GTAAACTCAT GCTTTCCTGT GCCATCCGCA GGACCCTCAG 900
TGCAGGTCAA TCTCCCCTCC ATTTCAGGGA ATCCAGGCTC CAAAAGGACA CAGGACTTGC 960
CCAGCAAGGT CATGTGGTGA GGTGAGAGCC CAGCCAGGAC TGGTCCCCCC TTTTCATCAA 1020
TCAAGCTTAT GCTCTGGAAA TCTATCTGGC GAAGCCAGGA AAACTGGACA CTCTCCTGCT 1080
CCTTGGTTAT TCCCTGAGAA AATGCCAGCA GAAGCAGAGA AAAGCACGTC CCAGGGGTTA 1140
TGCATTTTGG GGAGGAAGGG AAAAAAAGAG ACCAGTGTTT AGGCAGCCGG GGGATGTTAA 1200
GTAAAAATAT CTCCTCGCTT TCAACGGAGT GAGCGTGTGT CATATTTCAG CCTGATGTGG 1260
TTTGTGAAGT TGGAGACCAC AGGCAGGCTC AGTTCCTGCT GCTGGCCAGC TTCCCCTTCC 1320
CTCTGTCCCT CCCCTGCCAT ATGCCTGCTC TCGTCTGCCC TGCCTGGGAC CACATCAGCA 1380
ATTTAAGAAT AGGGCAGAGA AAAGCAGTGG GTGTTGTGGG CAAGGGTAGG CAGCTGAAGG 1440
CCTGGGCTTG GGTCCTGGCT TTGCCAGTGA CAAAGTACTG GGTGACTTGG GCTAATGCAT 1500
GCCTTTCTCT GGGCCCCAGT GTCCATTCTG CACTGTAGGG TGGACAGCAT AATGTCAGCC 1560
TTCCCAGCTC TGATGGCCTC TGAGTTGGAG GGCTTTGTGC TCCCCACATG TACTTGGGTC 1620
CGGCATGTCT GAGACACAAA GTGAGCCCGC AGTGGTGCAA CTGGTGATTC AGCTACTGTT 1680
CTTGAATTTA ATCTTTTCGG ACTGAATTGA TTGCCCCATT TTGCAGATAA GGGAGTTGAG 1740
GCCTAGGATT TGTTGATGTA TCCCATTCCC TGCTCTACAA GCAACAATAA TAAGGGCCAC 1800
CATATGTAAC ACACTTACTA TGTATGTTCA CCTTTTGCTT TCACTATCTG CTTTAATCTT 1860
TTAACAGATC TACGAGGGGA GAGATAGTGA CTCCATTTTA CAGATGAGGA AACTGAGGCT 1920
CAGTTTAGAA AAATGAAAGG ACTTACGTTC TCTTCTTTGA GTCTCACAAT AGTCCTGGGG 1980
TTGTCATTAT GTGACCCATT TTACCAGTGA GGAAACTCAG GCCTGGAGAC GTGAGCTCCT 2040
TTGCCCAGGG GTCCCCAGGG 2060