EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-11908 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr17:43369940-43372220 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs721579chr1743370481hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr17:43371336-43371351TGGACTTTGGTCTCT-7.31
MYCMA0147.3chr17:43370615-43370627GGGCACGTGGCT-6.18
PAX5MA0014.3chr17:43370191-43370203GAGCGTGACCTC+6.14
RREB1MA0073.1chr17:43371155-43371175TCCCCAAACACCACCTCCCA+6.67
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_01249chr17:43369797-43372371Adrenal_Gland
SE_04602chr17:43367359-43372240Brain_Anterior_Caudate
SE_11470chr17:43364690-43370274CD20
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: 2             
ChromosomeStartEnd
chr174337097443371161
chr174337014743370559
Number: 1             
IDChromosomeStartEnd
GH17I045290chr174336802843375075
Enhancer Sequence
AAAGTCTAAG GGGTGTTCTG ACATCCAATT AGGCAAAAGC CCTTCAAGGC TGGCTATGCT 60
TCTTGTAACT GTACTTTCAT CCCACCTCAC ACCTCCCCAC CCCACTCTAC CTCCAAAAAA 120
GAAACTGACC TAAGCCCAGA GCCGATCCCA CTGTTCTCAG CCTCTTTACC AGGGGAAATG 180
AGATCTTAAG AACAGACCAA AAAGTCTCCA AACCTAACAG CAGTAGGGAA TGCTCACAGG 240
GAGCTCGATG TGAGCGTGAC CTCCTCATTT CTATTTGAAG AAGCTGAGGC CTAATTCAGT 300
GGAGACTTGC CCAAGGTCAC CCAACCCACG TGTGACAGGA CATGGCCAGG ATCCAGACCC 360
TAGGTTCTTT AGGCTATGAT GCCCACTCCC CAAGCTCCTG GGTTACAGGC AAATGCAGGA 420
GGGCACACTA AGGTCCTCCC TGGTCAACAG GCTCCTGAGG GAAGAGGTGG GGCCCTGCAC 480
ACAGTGCCTC CCCAGTGTAT AGCACAGGGG CCACAGACCA CGCAACTGAC GCTGGCTGAA 540
CGAGGGACTC AAAGGACAAA GATTGCTTTT CCATAACCTT TGGAGACAGG ATGATCCCGA 600
ATGCTGAGGA GGAAGAGAGA GTCCTGCCTG ATGAATGAGA AAAATGAGGC CAGGTGGTGC 660
AGTTGCTGCT CTGAGGGGCA CGTGGCTATT AGAGATCTGG CTGTGTGGGG GCTCTGATAG 720
CCTGTCTCCG CCTGGCATGG CCCAACGGAG GCTTCTGGAT AGGTCATCCT GAGCTAGAAC 780
TCCTCCAGAG GGGGTGCAGG GCATCCCGAG TCCCAGAGTT GTCCTTTCAT ATTGGTGTTA 840
GGTAGGCAGC TGTCCAGCGC CCCTCTGTGA GCACACCAGG CTCCCCTCTT CCCAGAGAAG 900
TGGAAGCTGA GGCTGAGGCA GCCACGCTCA GAGACTCCTT TGCAGTTCCC CGATGACTCA 960
TCCAACAGCC TGGCAGGCAG ACAGTAACAA GGAGGCTGTT GAGAAGCTGA CCCAGCAGAT 1020
GGCAGCTGAA CTTGTGAAGG ACATGGGGAA AACAGGCTGA CCCTCACCTC TCAGGGGCAC 1080
AAATCACGGC CTGGGAGCTG TAAAGCTCCT CCTGTGGCTG GCTTTTCTGT GCCACATCAC 1140
CATGACTCAG ACCCTCACCG ACAGCCTCCA AGTTCAAGAG GCTATTCTTG GGACACTTTG 1200
GCCTGACAGT GGCTCTCCCC AAACACCACC TCCCACACAG ACACACATGC ACACACACAC 1260
ATGCACACAC AGACACACAC ACATACGGAT GCACTTGCTC CCTCCCTCCT TTCCTAATTC 1320
TATCTGGACT CTGGTCTACA AAAATCATGG TTCTGTACTA AGTCCAGGAC TACTGGCCAG 1380
GGGGCCTTCC CAGCCCTGGA CTTTGGTCTC TGGCTGTCAC CCCAGCTCAT GGCCCTAACA 1440
CTTTGCCCCT TCTCCCTCCT GCAGCGTGTG GGGAGGACGA AGTGGGAGCC AGTTATGTCT 1500
CTGCCTTTGA AGGCAAGTCA AACTCCTGAT TCATTCCTCA GCCTAGACAC TCTCCTCAGC 1560
TTATTCACGC CCCAAAGGCA TTGGGCCCTC TACTCTCTGC ATAAGAGTTG AGGACACGAG 1620
CAGTGGCAAC AGCCAAACCC ACATGGCTCA CCCATAAGCC CAAGAAATCA GAAGAGGAAA 1680
GGAAAGGAGC AGAATTCACT CCATATTCTT TGAGGCCTGA TGCACAGACA CTGTTGGTTC 1740
TTTCTTCTGT GATGCCTCAG TGACCTCCTG GAGAAGCCTG GGGGATAGGA ATGATCTGGA 1800
CAGTACCAGA TCAACCTCTG GGCATAGCTG TATGAGGAGT TCTTAATCTA GGTTCAAGGA 1860
TGGATTCAGG GAGAAAAATG TAATTTGCAT TTTTCCAGGG AAGACTTGGT CCATAGCTTT 1920
CAACAGATTC TCCAAGGATC TGCCATTCCC CAGAAGGTTC CTCTAGTCTC CCTAGAAAAT 1980
CAGGGCCGGG CTAAATGCCT GATTCTGGCT CTATTCTTCC ACTCCGAGGA AAAGCTCTCC 2040
AATGCAGCAG TTTCCAATCT GACCACAGAT TAGAATAACC AGATAAGTTC TTTAAATGCA 2100
TTCCTCCTAG GCCTGCTGAA CCAGTCACTG GGCATTAGGC CCAGAATCTG TACTTTTGAC 2160
AAGTTCTCTG GATGATTCTG ATGCCAAAGG GCCAGAGACT GCCACCTGAC CCCTGCTCTG 2220
TACTCAAGGC GACACTGTCC AAAATGGTAG CCACTAGCAA CATGTGGCTA TTTACATTTA 2280