EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-46692 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr5:150458120-150460440 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10036748chr5150458146hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr5:150460395-150460413CCTCCCTTCCTCCCCTCC-6.88
EWSR1-FLI1MA0149.1chr5:150460399-150460417CCTTCCTCCCCTCCATCC-7.16
ZNF263MA0528.1chr5:150460395-150460416CCTCCCTTCCTCCCCTCCATC-6.84
Number of super-enhancer constituents: 52             
IDCoordinateTissue/cell
SE_01392chr5:150459909-150461440Adrenal_Gland
SE_02605chr5:150457931-150461683Astrocytes
SE_09226chr5:150457220-150463541CD14
SE_13196chr5:150458636-150462213CD34_Primary_RO01480
SE_13605chr5:150457295-150463074CD34_Primary_RO01536
SE_15204chr5:150457060-150464046CD4_Memory_Primary_7pool
SE_17136chr5:150457478-150459064CD4p_CD225int_CD127p_Tmem
SE_17136chr5:150459089-150463722CD4p_CD225int_CD127p_Tmem
SE_17941chr5:150455174-150468518CD4p_CD25-_CD45ROp_Memory
SE_18317chr5:150453499-150468432CD4p_CD25-_Il17-_PMAstim_Th
SE_19111chr5:150454771-150468362CD4p_CD25-_Il17p_PMAstim_Th17
SE_23141chr5:150459423-150463805Colon_Crypt_1
SE_23836chr5:150458383-150458852Colon_Crypt_2
SE_23836chr5:150459524-150460010Colon_Crypt_2
SE_23836chr5:150460015-150461432Colon_Crypt_2
SE_25002chr5:150459756-150463818Colon_Crypt_3
SE_25989chr5:150459020-150467086Duodenum_Smooth_Muscle
SE_27123chr5:150458078-150459004Esophagus
SE_27123chr5:150459486-150463835Esophagus
SE_28253chr5:150459575-150463862Fetal_Intestine
SE_30354chr5:150459562-150463888Fetal_Muscle
SE_31853chr5:150458263-150458951Gastric
SE_31853chr5:150459483-150461612Gastric
SE_32472chr5:150457038-150467121GM12878
SE_35096chr5:150459004-150467156HeLa
SE_36009chr5:150458119-150466450HMEC
SE_37013chr5:150457760-150468647HSMMtube
SE_40909chr5:150457472-150463321Left_Ventricle
SE_42116chr5:150458117-150459039Lung
SE_42116chr5:150459403-150463856Lung
SE_47695chr5:150458379-150458918Pancreas
SE_47695chr5:150460013-150461460Pancreas
SE_48252chr5:150457890-150463826Psoas_Muscle
SE_48796chr5:150458085-150459028Right_Atrium
SE_48796chr5:150459381-150461672Right_Atrium
SE_50074chr5:150457386-150459056Sigmoid_Colon
SE_50074chr5:150459210-150463852Sigmoid_Colon
SE_51316chr5:150457386-150463718Skeletal_Muscle
SE_51803chr5:150457901-150463858Skeletal_Muscle_Myoblast
SE_52353chr5:150456814-150459032Small_Intestine
SE_52353chr5:150459333-150463840Small_Intestine
SE_53309chr5:150456880-150463266Spleen
SE_56023chr5:150457252-150463877u87
SE_57972chr5:150459934-150461443VACO_9m
SE_58791chr5:150431451-150475486Ly1
SE_59083chr5:150437761-150478457Ly3
SE_60748chr5:150431201-150478526DHL6
SE_61344chr5:150438255-150475360HBL1
SE_62297chr5:150437930-150538770Tonsil
SE_63588chr5:150457856-150463874HSMM
SE_64498chr5:150459057-150464080NHEK
SE_67545chr5:150457252-150463877u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5150458197150458752
Enhancer Sequence
ACGTATGAGA AAAATAAAAT AGTAACGTGA CAGAAAGTGA AAAAAGGGGC TGCTTTGCAT 60
AAAAAGATCA GGGAAGGCCC CTCTGAGGAG CTGACATTTG AGCTGAGACT TGATCGATAA 120
GGAAAAACCA GCCATGGGAA AAACGGGGAA AGATGTCCTG GGCAGAGGGA ACAGCATGTA 180
TGAAAGCCTA AGGATGAGAA CAAGCTTGGC TTGCTGGAGG GGGAAAAGCA GGCCAGCATG 240
GTGTGACCAA ATCACAGCGG GTACAGGAGT AAAACAGTAA CCAGTGGGTT GGAGAGAGAG 300
GCAGACAAAC AACCTCCTAC AACGCTGCCT CTCTCAAATC AGGTCGGCCT GACCCAACCA 360
GGACATCCGG GCCCCAAGTC ACAGGCAGCA CTGGGGGTAA GGGTATGACT CAGACCCCAC 420
AGCTTCCTGG GGCCCCGAAA AAACTGGTGG GGGTATCCAG GGGCAGGCAT CAACCTTCAG 480
CATGAGTGCC ATGCCATACC CATGGAACAC CCAAGGCTGG GAGACAAACG TGGTTACATA 540
AGCGTGTAGA ACACTGCACA CTCCCAGCGG CAGCTTCCAG AGGGGCATGA TCACGTGCTT 600
CCATGAAGTG CCAGTCCCTG ATCACATTAT TTTCCCGGGA CACAGCCAGG ACAGCAGCCT 660
TGGTCAGGGG AAAGGGAACA GGGTCCAGGA TTCAAGCGTT GCTAGTCTTG GGAAAGCCTT 720
AACCTTCTCT GGGCCTCAGT TTCCTCATCT GAAAATTAAG AGTTGTTAGA AAGATTAAGT 780
GAGGCCGGGC GGGGCGGCTC ACACCTGTGA TCCCAGCACT TTAGGAGGCT GAGACGGGCG 840
GATCACTTGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC ATGGTGAAAC TGTCTCTACT 900
CAAAATACAA AAAAATTAGC CGGGGATGGT GGCGAGTGCC TGTAATCCCA GCTACTCGGG 960
AGGCTGAGGT AGGAGAATCG CTTGAACCTG GGAGGCAAGT TGCCGTGAGC CGAGATCGTG 1020
CCACTGCACT CCAGCCTGGG TAACAGAGTG AGACTCTGTC TCAAAAAAAA AAAAAAGATT 1080
AAATGAGATA CGGAATGTAA GCACTGTGCC TGGCACATAG TAAGCTATTA GCATTATCAG 1140
TTTTTTCACT GCCTCAGTTT CTTCTGTTGC AAAACAGAGA CCACCACGGG GATGCTGAGT 1200
TTGTACTAAT ATTCTACCCT CCTAATACAA TTCTACCCTC CTTTGTCAAG GATTTTTTTA 1260
AAACATTCTG AGTCCCCTTT TCTGACCTCT CATCAGATGC CGAATTCCCC TCTATCACAC 1320
CCCATTGTTT GGAAAATGAG TAAGTGCTGA TTAAATCCCA TTTTGACCGT ACTGTGAGAA 1380
AAAAATGATG CATTAGGAAT CTACACATTT CCCTGCACTG TCATTCTGCA AGGGGGTGGG 1440
GAAGGACGTT GCTGATTCTT CTGCATCATC CACAAAAGTC CCTCCCTCCC CCTACCAAAA 1500
CACAATCTCT CACCCAGTCG CACAAAATTC CCATCTGCTC CTGTACGCAC AATGAATGTA 1560
CAATGCACAC GTGCACACAA ATGTCCTACA GTGGAAAGCT CAGCCTTCAT ACTCCATCCC 1620
CAGAAGCACT CCTGGAAACT CATCCATCCT GCACATGCAC ACAAATGCCT CCAACAATGT 1680
GCATACAAAA TATGTTCAAC AGAAATAGTA TAGTAGGAAC TCTGGAGCCA AATGCCTGAG 1740
TTCATATCTG ACTTTGCAAC TCACAGCTGT GTGACCTCAA GCTCCAAGTA CCTCGGTTTC 1800
CTAAAGTATA AAATGGAGAT AATAACAATA TTAATGTTTA GGATGGAAGT GACAATTAAA 1860
TGAGTCTAAT ACACGTACAG CGTTAAGATC AGCACTTGGA AAGCGCCCAA TAAAAATTAT 1920
TATTTTCCTC CTCGTGACAT ATGTACACTG CTTCCACAAC TTGATACGAA AACTCCTGAC 1980
GCCGCGTAGG CAACTCGTCT CCACAGGATA GACACCCAAA GGGCCGCAGC GCCGCCCGCA 2040
CCCGGAGGGT CTGCGCTCTC TACAACCGCC CCACGCCGTT CCCAGGCGTG CTACCCCGCG 2100
CAGTGCGCAC GCGCGCCCCC CACCAGGCCC AGCGCCAAGC AGGGAGTAGC GGCTCAGCCC 2160
GGCTTGGCCG CTGGCGGAGA CGCCCCGGGA CCCCGCGCGC CGGGCCTGGG TGCACAAGCC 2220
ACCTTCCCCA GCTCGCTCCC CGCCGCCACC GAGGCTCTGG ACGATCTGGG CCTGGCCTCC 2280
CTTCCTCCCC TCCATCCCCG CTCCGGGCCG GCCGGCTTAC 2320