EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS179-06827 
Organism
Homo sapiens 
Tissue/cell
SkMC 
Coordinate
chr11:65252430-65253890 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs587080chr1165253800hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr11:65252868-65252889AAAAAAAAAGAGAAAGTTTAT-6.38
Number of super-enhancer constituents: 49             
IDCoordinateTissue/cell
SE_00028chr11:65250988-65277615Adipose_Nuclei
SE_00879chr11:65253195-65254978Adrenal_Gland
SE_01577chr11:65252760-65253733Aorta
SE_03165chr11:65252854-65253723Brain_Angular_Gyrus
SE_03882chr11:65252507-65262880Brain_Anterior_Caudate
SE_04846chr11:65252181-65262791Brain_Cingulate_Gyrus
SE_05895chr11:65250838-65275661Brain_Hippocampus_Middle
SE_06693chr11:65252147-65276599Brain_Hippocampus_Middle_150
SE_07762chr11:65250696-65262852Brain_Inferior_Temporal_Lobe
SE_08788chr11:65252858-65253137Brain_Mid_Frontal_Lobe
SE_08788chr11:65253420-65253674Brain_Mid_Frontal_Lobe
SE_25770chr11:65252372-65276621Duodenum_Smooth_Muscle
SE_26547chr11:65252543-65262946Esophagus
SE_28555chr11:65252858-65262651Fetal_Intestine_Large
SE_29556chr11:65252771-65276612Fetal_Muscle
SE_31424chr11:65252932-65262941Gastric
SE_33445chr11:65252127-65258476H2171
SE_34266chr11:65252073-65262837HCT-116
SE_34617chr11:65237426-65277580HeLa
SE_35831chr11:65252552-65262853HMEC
SE_36925chr11:65252260-65275698HSMMtube
SE_40612chr11:65252729-65253785Left_Ventricle
SE_42107chr11:65253153-65253776Lung
SE_44137chr11:65252735-65262954NHDF-Ad
SE_44750chr11:65252712-65253727NHLF
SE_45562chr11:65252799-65275714Osteoblasts
SE_46695chr11:65253349-65253631Ovary
SE_47127chr11:65243490-65277571Panc1
SE_51077chr11:65252635-65277472Skeletal_Muscle
SE_52357chr11:65252816-65253709Small_Intestine
SE_54503chr11:65243495-65276614Stomach_Smooth_Muscle
SE_55732chr11:65252807-65255220u87
SE_56764chr11:65253325-65253631VACO_400
SE_57928chr11:65253320-65253614VACO_9m
SE_58932chr11:65238587-65276390Ly3
SE_59720chr11:65237780-65272476Ly4
SE_60674chr11:65238641-65271340DHL6
SE_61239chr11:65237836-65278618HBL1
SE_62240chr11:65238321-65275907Tonsil
SE_63249chr11:65244238-65267283GLC16
SE_63391chr11:65243820-65268347NCI-H69
SE_64233chr11:65252819-65253822NHEK
SE_65450chr11:65253579-65270152Pancreatic_islets
SE_66874chr11:65252127-65258476H2171
SE_67468chr11:65252807-65255220u87
SE_68042chr11:65238458-65277023TC32
SE_68043chr11:65238458-65277023TC32
SE_68495chr11:65243635-65267694TC71
SE_68496chr11:65243635-65267694TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116525320065253546
chr116525283165253647
Enhancer Sequence
TCCCAAATAC AAAATTATAA CAAAATTACC CTGCACTGTC ACCACCGTTT CATAAGAAAA 60
AAGTCTTTAT AACATCAAAG ATACAAGAAG GGCTTGTGAA CCCAAAATAT CTGAGACAGG 120
TCTCAACCAA TTTAGAAGGT TTATTTTGCC AGCCGGGCAC GGTGGCTAAC ACCTGTAATC 180
CCAGCACTTT GAGAGGCTGA GGAGGGTGGA TCTTGAGGTC AGGAGTTTGA GACCAGCCTG 240
CCCAACATAG TGAAACCCTG TCTCTACTAA AAATACAAAA AATTAGCTGG GCATGATGGC 300
GGGCGCCTGT AATCCCAGCT ACTTGGGAGA CTGAGGCAGG AGAATTGCTT GAACCTGTGA 360
GGTGGAGGTT GCAGTGAGGC GGGATCGTGC CACTGCACTC TAGCCCGGGC GACAGTGCAA 420
GACTCCGTCT CAAAAAACAA AAAAAAAGAG AAAGTTTATT TTGCCAAGGT TAAGGACACA 480
CCCATGACAC AGCCTCGGGA GGTAGATAAG AGACAAAGAG TTGCACTCTT TTCTTTTGAG 540
TTTCTGATTA GCCTTTCACC TAATACGCAA TTTACATTTG AGAGGAGGGC AGAGGAGTAG 600
TCACTTTTGC TTTAGTCTGG TTTAGTGAAA TCAGAGGTCA GGGGAAGCAA TCCGATATGC 660
ATTAGTCTCA CGTGAGCCTC GGAGGGATGA TTTTGAGTTC TGTCTGTCCT TTGTCCACAA 720
GGAATTTCCT TGTGGGCAAA TTGTGAGGGA GGCATGTAGC TTTTTTTTTA ATAAATCTTT 780
GTAGCTATCT TATTTAGGGA TAAAATTGGA AGCAGGTTTG CCTGACATAG TTCCCAGCTT 840
GACTTTTCCC TTGGCTTAGT GATTTTGGGA TTCCAAGATT TATTTTCCTT TCACAGGCTT 900
AATCTCTGAA TAAAGGACCC TCTTAAAATG GGATGTAGTT AGTTTTCTGG AAAAGTCACA 960
GCCGACGCTC CCAGGGACTG TTTCTGGTTC ACGGGCCCTA GGTTCAAACA ACCCTTCCCA 1020
AACCTTGTTT GTTTCAAAGG TTGAGATCAA AGCTAGTGGG TAGCCAGTGA GGCTGTGCTT 1080
GTTCACTCTG TGACTCGGAC AAGCTGGCAC CTGTCTTCTC TGGGCTGCTT TCTCTCAAAG 1140
ACTAAGAGTG TTTAGTGCAG AAAGGCCCTC AGAGATCTGG GTTAACCTCT TATTTATTTA 1200
TTTTTATTTT TTGTTTTGTT TTGTTGTTTT TGAGATGGAG TCTCACTCTG TCGCCCAGGC 1260
TGGAGTGCAA TGGCACGATC TTGGCTCACT GCAACCTCTG CCTCCCGGGT TCAAGCGATT 1320
CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA TTACAGGCGT ATGTCACCAA ACCCAGCTAA 1380
TTTTTGTGTT TTGAGTAGAG ACAGGGTTTC GCCATGTTGG CCAGGCTGGT CTCGAACTCC 1440
TGACCTCAGA TGATCTGCCC 1460