EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS028-02593 
Organism
Homo sapiens 
Tissue/cell
Colo829 
Coordinate
chr3:42093130-42095170 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1498095chr342093422hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RELMA0101.1chr3:42094179-42094189GGGGATTTCC+6.02
ZBTB18MA0698.1chr3:42093373-42093386TATCCAGATGTGT+6.52
ZNF740MA0753.2chr3:42094869-42094882GGGGGGGGGGCGG-6.64
ZNF740MA0753.2chr3:42094865-42094878GTGGGGGGGGGGG-6.92
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00063chr3:42092425-42097420Adipose_Nuclei
SE_01171chr3:42093532-42095450Adrenal_Gland
SE_01796chr3:42093170-42096158Aorta
SE_02512chr3:42093454-42094851Astrocytes
SE_10922chr3:42092287-42111479CD20
SE_23272chr3:42093552-42094870Colon_Crypt_1
SE_23272chr3:42094873-42095350Colon_Crypt_1
SE_25861chr3:42092606-42095935Duodenum_Smooth_Muscle
SE_26989chr3:42093342-42095507Esophagus
SE_29565chr3:42093028-42096170Fetal_Muscle
SE_36966chr3:42092627-42095822HSMMtube
SE_38230chr3:42092646-42095313HUVEC
SE_40683chr3:42092524-42096138Left_Ventricle
SE_42248chr3:42092644-42096169Lung
SE_44342chr3:42092481-42096334NHDF-Ad
SE_44918chr3:42092630-42094832NHLF
SE_45733chr3:42092534-42097909Osteoblasts
SE_48185chr3:42092500-42096165Psoas_Muscle
SE_48670chr3:42092710-42096154Right_Atrium
SE_49555chr3:42094889-42095394Right_Ventricle
SE_50309chr3:42092613-42096199Sigmoid_Colon
SE_51166chr3:42092564-42096576Skeletal_Muscle
SE_51885chr3:42094060-42094792Skeletal_Muscle_Myoblast
SE_52625chr3:42092703-42095816Small_Intestine
SE_53513chr3:42093436-42094956Spleen
SE_54717chr3:42092721-42096159Stomach_Smooth_Muscle
SE_62800chr3:42053253-42125059Tonsil
SE_63663chr3:42093585-42094806HSMM
SE_65769chr3:42094487-42095477Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr34209334142093564
Number: 1             
IDChromosomeStartEnd
GH03I042051chr34209262842097539
Enhancer Sequence
TGGACCAGCT TGAGCAGCTG AGTGGCTATT CGATGGCCCA CGACCTGAGT GAACTGGCCT 60
TCAAAGGCTC AGAGGAGATG GCTAGCCCTT TGCTACTTGC ACTTGAATGA GCCATTATGA 120
GAAAGATAGG ATGGAGAATT CTGAGTGATC TGGGAGACTG AGAGACCTTT ATCTTTTAAG 180
ACATGAAAGA CAATGGAGGT CTGGCTGCTT CACCCCCAAT TCCCAGAATA CAGTCCTGGT 240
GGCTATCCAG ATGTGTGTGG CTGAGATTTT TTTCCTTCTT AAACTTATTC CTCTTTGAGC 300
CCTATCTTCT CTACTACCCA GTGACGTGAC TCATTTGGAA GCCACCCTGT GCCTTTGTGA 360
TATGACAGCT TAGCATGTGA CCAGCTTTTG AATGATTAAA TCTGCAGACT CCATCAGAAG 420
CAAGGAGTAA TCTGTGAAGT CCAAACTCAC AAAGTAGTTA AAGATGATTA TAAATTAAAG 480
AAGCACCACC TGGGCGGGTC TCTAAGGGAC ATGGCATCAG CCCTGTGCTG AACAGTCCAT 540
TGTGTCATAT CTTAGGGATT ATGTGGCTTG ACATTACTTG CTCTTTCAGC AGTAGCCCTC 600
ACTATAGTCC CCAACCAGTA CCGTCAGCAT CACTGGGAGC TTGTCAGAAA TGCAAATTCT 660
TGGGTCTTCA GACCTCAGAA ACTCAGGCAT GGGGGCCCAG CAATCTGTGT TCTAACAAGC 720
CCTTCAGGAG ATTCTGATGC TCTTTACTGG TTTAGATGAT CTTGTAGACT GGTGCAAAAG 780
TCAGTCCTTC TGGGTTTGGG GGTTGCTCCC ACATAGCCTG GAAGGAGGGA ACAGTAGTCT 840
TATCTGAGGC TTCCTCAGGG AAATAACCCT CCAGCTTAAG GCCTCTTATG CTATTGTTGA 900
GCAGATTCAG CCTCTGATTT AGGAAAGTAG CCAATTGGAG CAAAAAGCAT GATTCAGTCT 960
TGAAGGAAAA AAATAACTTG GGCTACTCTG CGTCATGTGA AGAAGTAACT GGGTCTCGTG 1020
TGGATGCCAG TGATAACAGT TGGCATACTG GGGATTTCCT TCTAATCTTT ATTCTGTGTG 1080
CATGCAGGAT GTGCATTTAA TCTAGTTGGG ATCCCATTGT ATGCATTGTT CTGTATTGCC 1140
CCCTCCCCCA TTATGAAAGA GTCCCGTGAC ACCACAGTGT TAAGGACTGA GGTGGTAAGG 1200
GCTCCAGGAT GTCAGTGGCT ATCAGAGGTC CCCAGCTCTG AGAAAACTGG TGGCTGAATG 1260
CGTAGTCCCC GAAGAAGTCA TTTTCCCAAG GCATTTGGAG TTGTTGGTGC TACTGGCACA 1320
TTTTGGACCT CTGTTAAGGG GAAAGACAGG GGGAGCTGAC TGACTGGGCT ACTCCATTGC 1380
CATTTAGATT TCCTGACTCT GCAAGCTGGC TGAATGTTGC TTTTTCATGT GCTGCCTGGA 1440
CTAAAGCTGT CTGATTCTTT CCTTCTGAAC AATGGCTGTT TTTATGAGAT CTTGCTTCTC 1500
CCAGGCAGTG GCCCACACAG TGAAGTCTTT TCTTTCCCGT TTGTGTAAGC TAGTGGACCT 1560
TATGGACTCT GTCTGGCTGA CTTTTCTCTA ATGTTTACAG TTCGTGTAGT GTGATAGCCG 1620
AGCTCATTTT CCGTGTGAAG AAAAAGAAAA GGTGGATAAT GGACCGCCTC CCCCTCCCTG 1680
CCTCCAGAAA AAAAGGCACT CAGAGAGAAA AGACTGCAGT CCCATTCAGA GTCGGGTGGG 1740
GGGGGGGGGC GGGGGATGGC AAAGGGGGAG GGTAAAAGAG GACCCTTAGG GCAAATGACT 1800
GTTCTGGGGA TGGGGTGGGG AGTCAGCCTT CTTGGGGGAG CTGGGGATAC TTTGTGTAGG 1860
GCCCCATTCT GTGGTATGGG CTTCTTTCCT CCTGGACCCT GGTGTAGGCT GGAGAAATCA 1920
GTATTATGGA AGCCACTGCC TCCTCACCCC GCCCCCAGGA TCTAGGCCCA GAGGACCTGG 1980
CAAAAGCTGG GTTGGCACCC ACACCCAGGA CCTGCCCGAG CCAAGTCCAC GCTGCCCCTG 2040