EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS086-05442 
Organism
Homo sapiens 
Tissue/cell
HEK293 
Coordinate
chr17:43370290-43371580 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs721579chr1743370481hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr17:43371336-43371351TGGACTTTGGTCTCT-7.31
MYCMA0147.3chr17:43370615-43370627GGGCACGTGGCT-6.18
RREB1MA0073.1chr17:43371155-43371175TCCCCAAACACCACCTCCCA+6.67
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01249chr17:43369797-43372371Adrenal_Gland
SE_04602chr17:43367359-43372240Brain_Anterior_Caudate
SE_11470chr17:43370585-43396257CD20
SE_15206chr17:43369767-43372845CD4_Memory_Primary_7pool
SE_18500chr17:43366366-43375242CD4p_CD25-_Il17-_PMAstim_Th
SE_19630chr17:43370599-43371979CD4p_CD25-_Il17p_PMAstim_Th17
SE_23493chr17:43370233-43371784Colon_Crypt_1
SE_24167chr17:43370547-43371576Colon_Crypt_2
SE_25878chr17:43364447-43377187Duodenum_Smooth_Muscle
SE_26725chr17:43369959-43372440Esophagus
SE_30018chr17:43370009-43372329Fetal_Muscle
SE_31611chr17:43370038-43372444Gastric
SE_32589chr17:43370933-43372485GM12878
SE_34075chr17:43370326-43375105HCC1954
SE_40748chr17:43363700-43375200Left_Ventricle
SE_41691chr17:43369983-43371993LNCaP
SE_44657chr17:43370169-43372693NHDF-Ad
SE_46201chr17:43369956-43372823Osteoblasts
SE_47195chr17:43366097-43378703Panc1
SE_48714chr17:43365874-43374860Right_Atrium
SE_49545chr17:43369873-43372224Right_Ventricle
SE_50169chr17:43369845-43372240Sigmoid_Colon
SE_51970chr17:43369906-43372027Skeletal_Muscle_Myoblast
SE_54723chr17:43359357-43378642Stomach_Smooth_Muscle
SE_59053chr17:43370566-43412054Ly3
SE_62481chr17:43366079-43396493Tonsil
SE_63770chr17:43369873-43372185HSMM
SE_65719chr17:43369005-43372029Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174337097443371161
Number: 1             
IDChromosomeStartEnd
GH17I045290chr174336802843375075
Enhancer Sequence
ATCCAGACCC TAGGTTCTTT AGGCTATGAT GCCCACTCCC CAAGCTCCTG GGTTACAGGC 60
AAATGCAGGA GGGCACACTA AGGTCCTCCC TGGTCAACAG GCTCCTGAGG GAAGAGGTGG 120
GGCCCTGCAC ACAGTGCCTC CCCAGTGTAT AGCACAGGGG CCACAGACCA CGCAACTGAC 180
GCTGGCTGAA CGAGGGACTC AAAGGACAAA GATTGCTTTT CCATAACCTT TGGAGACAGG 240
ATGATCCCGA ATGCTGAGGA GGAAGAGAGA GTCCTGCCTG ATGAATGAGA AAAATGAGGC 300
CAGGTGGTGC AGTTGCTGCT CTGAGGGGCA CGTGGCTATT AGAGATCTGG CTGTGTGGGG 360
GCTCTGATAG CCTGTCTCCG CCTGGCATGG CCCAACGGAG GCTTCTGGAT AGGTCATCCT 420
GAGCTAGAAC TCCTCCAGAG GGGGTGCAGG GCATCCCGAG TCCCAGAGTT GTCCTTTCAT 480
ATTGGTGTTA GGTAGGCAGC TGTCCAGCGC CCCTCTGTGA GCACACCAGG CTCCCCTCTT 540
CCCAGAGAAG TGGAAGCTGA GGCTGAGGCA GCCACGCTCA GAGACTCCTT TGCAGTTCCC 600
CGATGACTCA TCCAACAGCC TGGCAGGCAG ACAGTAACAA GGAGGCTGTT GAGAAGCTGA 660
CCCAGCAGAT GGCAGCTGAA CTTGTGAAGG ACATGGGGAA AACAGGCTGA CCCTCACCTC 720
TCAGGGGCAC AAATCACGGC CTGGGAGCTG TAAAGCTCCT CCTGTGGCTG GCTTTTCTGT 780
GCCACATCAC CATGACTCAG ACCCTCACCG ACAGCCTCCA AGTTCAAGAG GCTATTCTTG 840
GGACACTTTG GCCTGACAGT GGCTCTCCCC AAACACCACC TCCCACACAG ACACACATGC 900
ACACACACAC ATGCACACAC AGACACACAC ACATACGGAT GCACTTGCTC CCTCCCTCCT 960
TTCCTAATTC TATCTGGACT CTGGTCTACA AAAATCATGG TTCTGTACTA AGTCCAGGAC 1020
TACTGGCCAG GGGGCCTTCC CAGCCCTGGA CTTTGGTCTC TGGCTGTCAC CCCAGCTCAT 1080
GGCCCTAACA CTTTGCCCCT TCTCCCTCCT GCAGCGTGTG GGGAGGACGA AGTGGGAGCC 1140
AGTTATGTCT CTGCCTTTGA AGGCAAGTCA AACTCCTGAT TCATTCCTCA GCCTAGACAC 1200
TCTCCTCAGC TTATTCACGC CCCAAAGGCA TTGGGCCCTC TACTCTCTGC ATAAGAGTTG 1260
AGGACACGAG CAGTGGCAAC AGCCAAACCC 1290