EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-21903 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr7:130583640-130586040 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs157935chr7130585553hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxa2MA0047.2chr7:130585515-130585527TGTTTACTTAGG+7.22
Sox3MA0514.1chr7:130585549-130585559CCTTTGTTTT+6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00314chr7:130585244-130590497Adipose_Nuclei
SE_01091chr7:130584817-130585723Adrenal_Gland
SE_02143chr7:130584598-130587002Aorta
SE_02249chr7:130584462-130592697Astrocytes
SE_06076chr7:130584012-130588575Brain_Hippocampus_Middle
SE_07287chr7:130583885-130586783Brain_Hippocampus_Middle_150
SE_10895chr7:130577042-130589837CD20
SE_17783chr7:130584510-130591597CD4p_CD25-_CD45ROp_Memory
SE_19100chr7:130577109-130584053CD4p_CD25-_Il17p_PMAstim_Th17
SE_19100chr7:130584526-130587168CD4p_CD25-_Il17p_PMAstim_Th17
SE_25777chr7:130577081-130591193Duodenum_Smooth_Muscle
SE_31761chr7:130581254-130587020Gastric
SE_33932chr7:130583464-130587123HCC1954
SE_34244chr7:130577071-130604705HCT-116
SE_35868chr7:130585050-130591078HMEC
SE_37103chr7:130583463-130591198HSMMtube
SE_37956chr7:130584348-130593030HUVEC
SE_41380chr7:130584994-130591172Left_Ventricle
SE_42440chr7:130583439-130590036Lung
SE_44204chr7:130585012-130587138NHDF-Ad
SE_44753chr7:130583480-130584123NHLF
SE_44753chr7:130585031-130591268NHLF
SE_45983chr7:130577077-130593006Osteoblasts
SE_47121chr7:130564937-130614550Panc1
SE_49059chr7:130584475-130586978Right_Atrium
SE_50153chr7:130583440-130587115Sigmoid_Colon
SE_51131chr7:130577123-130591604Skeletal_Muscle
SE_51750chr7:130585221-130587009Skeletal_Muscle_Myoblast
SE_52512chr7:130583439-130587123Small_Intestine
SE_55680chr7:130583493-130592987u87
SE_56759chr7:130583475-130584334VACO_400
SE_56759chr7:130584337-130587085VACO_400
SE_57985chr7:130583496-130584504VACO_9m
SE_57985chr7:130584685-130586988VACO_9m
SE_62335chr7:130583609-130656051Tonsil
SE_63540chr7:130585207-130587121HSMM
SE_64255chr7:130583974-130585110NHEK
SE_64255chr7:130585285-130587136NHEK
SE_67458chr7:130583493-130592987u87
SE_67975chr7:130558852-130656695TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr7130584357130584800
chr7130583676130584341
Number: 1             
IDChromosomeStartEnd
GH07I130883chr7130568375130592959
Enhancer Sequence
TCACGTTGTT TGAACACCGG AACTTCAAGG CGTGCTTGAA CCACCTGATC AAAGGAGAAG 60
GGACTGAGGA CCAACAGGAG TGGGGCTAAA GGCATCCTTC TGCTCCAGTT TCCTGTGAAC 120
CCGCTCCTCT GAGGAAAGGA GTAGTCCCCA CGGAAGACAC AGGATCCTTC TGGGGGTCCT 180
CCTTGGCCAC GTCACACTTC CAGACTGTGT GGCGGGACAC TGACCATCAA GCCGACAGAC 240
GTGGGTTTTA AAGCTACGCC TTAAAATCAG CAACTCCCTT TCCTCATGAA TATTTTAGTG 300
TGTAATATAG AAGATGTTTT TACACTGAAT TAAAGTGCCT GCCACTGAAT CTTCCTGCTG 360
GAATTATGGG GGGTGGGAGG AGATGGAAAA AAAATCAATG TTTCAAAGCA GTCCTGATGT 420
GCTAAAAATA TCTCTCACTT CTCCTTTCAT CTGTCTGGTC ATTGTCCCAG ACGCAAGCTC 480
AGCACAGCCT CGCCCATACA ACATGTCGAA TCGCTGTCTA CCTCCACTTC TTAATCGGAC 540
AAAGAGAGAA TATTCTTTTT TTTTTTTTCC TTCCTCAGAC ATTAGTCCAA GATTACAGAC 600
TAGGATATAG CAACCTATTA TTCAAGAACA GCTTTTAAAG GTAGCTGCTT CAGACTGGCA 660
CTTCGGGAAA ACTTTGAAAG TAGACTCCTT TTTTTTTTTA ATGCTTATTT TAACTATAGA 720
TTGGTGATAA CGATTCAACC CCAGAGATCC AGCTAACTGT TGGCACAGAA ATCCTTAACG 780
CTACTCTCAA GCAAATAAGA TCTTGTAAGG GGAAACTCCT GCAAAATATA CCTTGTGAAC 840
AAGCTGCTCG CACCTCCTCT TGCAGCTGCA AAGATATTCT ACTCTATTGC TTAACTCGTG 900
ACCTTGAAAA AACTCCACCT TTCCTGCCAG CAGCTCCACT GCATCCACCT GTCCCTACAG 960
GTAGTAAAAG ATTAGACAAA ACAGAACCAC GTTTACACAA CACACTTCCG AGCCTCTCTT 1020
CCTTCTAGCC CCTGTCCCAC CCCCACTCCA AGGTCGAAGT TCATTTCTTG CAGGCTTCAC 1080
TTTTCAGGAT TAACCAACAC TGTGCTTTTT CATTCTGCTC AACACCAGTC CTTTGGCCTC 1140
ACAGTGCTCG CCTGTGTGGA ACACGCTGCA GCCACCAGGT CATCTGCTTT AGACCCAGCT 1200
CCATGTCAAG TCCTGTTACG GTCCCTCGGG CATATTGTCA TGCTCCTGGG CACCTGAAAA 1260
CTGACAACTG GTTTCAAATT TCTTACAATT TGCTTTTCTG GTCTATCCTT ATTTATTCCC 1320
CTCACAGTGA CATTCATAGG AAGAGGAAGT AGCAGGCAGT CTCTTGGGGA CGGGTCTCTC 1380
CTGAATACCT GGGGGGATGC CCTGGGCTGG GGAACCTCAC AGGGGCTCAT CAAGAGGTTC 1440
CAGGAGACAG AGTTCGAGAC CAGCCTGGCC AACATGGTAA AACCCCGTCT CTACTAAAAA 1500
TGTAATAATC AGCGAGGCGT GGTGGCTTGC ACCTATAATC TCAGCTACTT GGGAAACTGT 1560
GGCAGGAGAA TTGCTTGAAC CCGGGAGGCA GAGGTTGCAG TGAGTCGAGA TCATGCTACT 1620
GCACTCCAGA AGTGGAAGTA GCCACCACAC AGCTGCACCT GCCACCTCCT TCCCCACTCC 1680
AGGGCCTTTG AAATGTGCTG CTCTCTCTAT GCCGAGAGCT CTCACCCCTA CCCCCTGCAC 1740
CCACACATTC CTGCTCATCC CTTAGCTGAG ACCTTGGAAA TCACCTCCTC AGGGGACCAC 1800
TGGGAAGAAG GTCCTTTTCA TCTGAGTGCC TTCCCCTCAG GGCATGATTT TTCTTGGGCC 1860
ATTTTTTTTG GTATGTGTTT ACTTAGGTTC CATGATGACA GAGACCATGC CTTTGTTTTC 1920
ATCACTATCG TCTTCACCTC ACTGCCAACC AGTGCCTGGC ACACAGTAGG TGTTCAAGAA 1980
AGTTTTGCTG AATAAATGGA TGAACAATGA CATCAGCCTA CTTTGACCTC TTGAGTTCCT 2040
CTGATCTCTG AATGTTCTGG AGCAAGGACC TTTAACAGCA TCTCCATCTC TTCCTGGCCT 2100
TGCCGCCCCA CCCAGTAAAA CCATAATACT TGCTGGTATA GCCTCTTCCT GCAAATAAAA 2160
GTATACAAGG AGTTCAGAAC GGACACTCCA AACAAAGGGA TTTATGACCT TGGTCTCATG 2220
TTCTCTTGTG GTGGTAAAAT TCACTTTTCT ATGAAATTAA AAATTCCTCC CTTGAACAAC 2280
ATTGCCAGAG GTCCCCAGAA CAAGGCAAAA CTGGGTATTC AAAACTTTTT AAGTTTAGGA 2340
AACGCTGCCT GGAATCTCTA TTTCTCCCTC CTCTGGTTGC ATTCTATTCC TCAGGTTATG 2400