EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-46691 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr5:150454750-150457300 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3792783chr5150455732hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SP2MA0516.2chr5:150456429-150456446CAAAGCCCCACCCACAT+6.07
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_01392chr5:150455183-150456483Adrenal_Gland
SE_02605chr5:150454842-150456793Astrocytes
SE_09226chr5:150454881-150456345CD14
SE_15204chr5:150455351-150456738CD4_Memory_Primary_7pool
SE_17941chr5:150455174-150468518CD4p_CD25-_CD45ROp_Memory
SE_18317chr5:150453499-150468432CD4p_CD25-_Il17-_PMAstim_Th
SE_19111chr5:150454771-150468362CD4p_CD25-_Il17p_PMAstim_Th17
SE_23141chr5:150454841-150456487Colon_Crypt_1
SE_23836chr5:150455200-150456402Colon_Crypt_2
SE_25002chr5:150455220-150456142Colon_Crypt_3
SE_27123chr5:150453721-150456784Esophagus
SE_28253chr5:150455196-150456191Fetal_Intestine
SE_31853chr5:150454852-150456622Gastric
SE_32472chr5:150455256-150456379GM12878
SE_32472chr5:150457038-150467121GM12878
SE_35096chr5:150455032-150456331HeLa
SE_36009chr5:150453747-150457034HMEC
SE_37013chr5:150454502-150457000HSMMtube
SE_40909chr5:150454783-150457437Left_Ventricle
SE_42116chr5:150454765-150456478Lung
SE_47695chr5:150455440-150456016Pancreas
SE_48796chr5:150455153-150456074Right_Atrium
SE_50074chr5:150454947-150456817Sigmoid_Colon
SE_51316chr5:150455114-150456779Skeletal_Muscle
SE_51803chr5:150454642-150456818Skeletal_Muscle_Myoblast
SE_52353chr5:150454959-150456784Small_Intestine
SE_52353chr5:150456814-150459032Small_Intestine
SE_53309chr5:150455146-150456609Spleen
SE_53309chr5:150456880-150463266Spleen
SE_56023chr5:150454657-150457156u87
SE_58791chr5:150431451-150475486Ly1
SE_59083chr5:150437761-150478457Ly3
SE_60748chr5:150431201-150478526DHL6
SE_61344chr5:150438255-150475360HBL1
SE_62297chr5:150437930-150538770Tonsil
SE_63588chr5:150454628-150456818HSMM
SE_64498chr5:150454519-150456918NHEK
SE_67545chr5:150454657-150457156u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5150455274150456118
chr5150455023150455538
chr5150455260150455927
Enhancer Sequence
GTTTCTTGTT GGTGGCTGAT GAAGGAGAAA TTTCAACTGA TTGGAAATGT GTTATTTCTT 60
AAACCAGATG AGTGAGCATG TAGGTGCCTG CGTGTTACCC TCGGTATCTG AGAGACTCCT 120
TCAATTTTTC TTTTTTCTTT TTACTGTATT GTTTGCTTTT TTTCTGCTTC AACTTTTATT 180
TTAGATTCGG GGGGTACATG TGCAGGTTTG CTACCTGGGT ATACTGCGTG ATTTGGGTAG 240
GGGTGATCCC ATCACCTGGG TACTGAGCAT AGTTCCCAAC AGTTTTTCAA CTCTGCCTCC 300
CTCCCTCCCC ACTCTAGCAG TCCCCAGTGT CTACTGTTGC CATCTTTATG TCCATGAGGA 360
CCTGATATTT AGCTCCACTT ATAAGTGAGA AAATGCAGCA TTTGGTTTTC TGTTCCTGTG 420
TTAATGTGCT TAGGACAATA TTTTCTAAAA GTCTATGTTG CCAGTTTCCT GAGGACCAGA 480
TCACGCAGGA GTTGCACCTG CAGAGACAGA AGTGGGCTGG AGAGGGACCA GGGCTCCTAA 540
GTCTGCTGCT GAAGCTGACT ATAGCGAAGG CAAAGGACAA GTGGCCTGAA GGCCAACAGA 600
GAGCCTGGCC AATGCTCTGC CCAGTGGGTG GAGACTGAGC CAAAGGCCCT TGACTCATAG 660
GGCAGTCCCA TACCTGCCCT GGCCTCTCAG CATGACTCCT TGGTGACACA ACTCCCACAG 720
CACCCACACA CCTACACCCA CCTACCCCAC ACACACACCC CTGCCTGGGC TGCCCGGTTT 780
GTCCACTGTG TAGGTGCTCA AGGACGCAGA GCTCCTGCCT CTCAAGGAAC AGCCTCAGGG 840
TGAGGTCCCT GGGAGAGAAG AGTTCAGCTC TGCCCAGAGC AGCCCTCAGA CAAACAGCCA 900
GCTGCTGCTC ACCAGTCATC CATTCCAATC TGAAGAGTGA CTGTCCTGGG CCAGTCATGG 960
GAAAATCATC AAGAACTTCC CACAATGGTC ATGGTGGCCG CCAAGGTCTT TCTCTGGGGG 1020
TTGGGAGCTG TGCTCCCCCA CAAAACAAGG GGACCCAGCT GCCCTGTGCC TTCCTGTGGC 1080
AACTCTCTGG AGGATGCCTG GATACCCTCC CTACAGACGG CCAGGGATAG GAGGGGCAGG 1140
CACTGCAGGC ATGTGGGGGC ATAGCAGCAA GAATCTAGGA GGGCAGGCAC AGCAAGGCCT 1200
GGCCCAGAGG GAAACCAGGA GCTGCCAGAG CCAAAGAGAG GGTGACCCAA TCATTGGTTG 1260
TTATAGAGTT TTTAAGACTT GGAAGAGAAT GCCCTGAGAT GCCAGAGAGT GAAACATTTT 1320
CATTCTAAAG CTGGGAAACC AAAGTCGGCA AAGGCGAACA GACGTGCCCA CAGCCACATG 1380
GGACAGCAGT GGCACAGAAG AAATGCACAC CTCGTCCTCT GGTGGCCACT GTGCACTCTC 1440
TTACCACACC ATGCTACTGC TCAACCTCTC CCCCTCCCTC ACAGTGGTCA GGTAAGCAAT 1500
GAGGGAAAAT GATGGAGGTG AGAAAGGAAG AACCCGGGCT GATGTGGGCC CACAAAAGAA 1560
AGAAGTCTGG AATAACACTG GAAGGGGCTG CCTACGAGGT GGAAAGCGCC CTGATCCCAG 1620
GGGTCGGGGT CACGCAGAGG GGCACTGGGG CTGTTGAGGG AATGCAAGCC AGGTGTCTTC 1680
AAAGCCCCAC CCACATCTGA GTTTCCGCCA CTCCAAACAG GGACAGATGT TTGAGACAAA 1740
GCAAAGGACA ACTCATCCAG AGGGGACACA GCATGGACCA CAAGTGGCAG AGGGTTGAAG 1800
GCAAGTGTCT TAGTCTGCTT TCTGCAACTA TTCTGTTGAA TATCACAGAC TGGGTAATTT 1860
ATAAAGAACA AGTTTATTTG GCTCATGGTT CTGGATGATG AGAAATCCAA GTGCATGACA 1920
CCACCATCTG ACAAGGGTCA TGCCAAGGTG GAAGACAGAA GGAGAAAATG AGTGATTGAA 1980
ATAGAGAGTG TATTAGCCAA ACTGGCCCCT TTTATAACTA ACCTCCCGTC CCCCTACCCC 2040
GTGATAGTGA CATTAATCTA TTTATGAGGG CAGAGCTGAC AATCCATTCA TGAAGCAGAG 2100
GGATTACGTT TCCAAGATAT GAACTTTTGG GGGACACATT CAAACCTTAG CAGCAAGTTA 2160
TCCAGAGCAC AGAAAATCAA ACCAGTCTCA TCATCTTCTA CTGGAATCCT GTCAATAGCC 2220
TCATGATTAG CATCATTAAC GATAATAGCA GCGACCCTGT ACCAAGCGCT TACCACACTG 2280
GTGGCCCGTG CTGAGTGCTT GCCACACACT ATCCCATTAA TTCCCACCAT TCTAGGAGGT 2340
AGCATTGACG TCATACAGAG CTGACAGGTG AGGATGCAGA GGCCCAGAGT GACAGACACG 2400
GCACCTACCC AGGTCTGCCA AGCACTGAAT CATGTGCTCT TCACCAGGGG TGCTCAAGGA 2460
GCAGCCCGGA CCAGCGGCAC TGGCACCACC ACCATCCACT GGATCGGATG CTCTGGAGTT 2520
GCAGCCCAGC AATCTGTGTT TAACAACCAC 2550