EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS068-04631 
Organism
Homo sapiens 
Tissue/cell
GM18526 
Coordinate
chr5:150453420-150456240 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3792783chr5150455732hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr5:150454616-150454627CATGAGTCACC-6.62
JUNDMA0491.1chr5:150454616-150454627CATGAGTCACC-6.02
ZNF263MA0528.1chr5:150453665-150453686AGAGGAAGGGGAAAGGAAGGA+6.36
Number of super-enhancer constituents: 35             
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_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_53309chr5:150455146-150456609Spleen
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
Number: 1             
IDChromosomeStartEnd
GH05I151071chr5150451179150453707
Enhancer Sequence
CTGAACTCCA GCCTGAGTGA CAGACTAATA CTCTGTCTCT TAAAAAAAAG AAAAGAAGAA 60
AAGAAAAAAG TCTCAAAGGA TACATACCAA ACTGCTACTA GTAGACTGCT CTACAGAAGG 120
ACCTCGGTAA GGAACTAAAA CCAAAAGAAA CTTTTATTTT ACCTATGCTA TTTTAACTCT 180
TTACATGGGA AATCTAGTCC TGTTCTTATA CAATTATAAA ATTAGTTTTT AAATACAGTA 240
GGGACAGAGG AAGGGGAAAG GAAGGAGAGA GAAGACAACT GTCATTTTTT ACATTATATC 300
TTTTGTACTG CTTGAGTTTT GGGGGGTTTT TCCCCAATAA TCATGTGCTA TTTGGTAATT 360
TTTTTTAAAG GGAAATTTTA AAATATTTTT CTAAAAAATT TAAGTGAGCT GAGTGCAGTG 420
GTGCATGCCT GTAGTCCCAG CTACTCCAGA GACAGACGCA GGAGGATGGC CTGAAACCAG 480
AGTTTATCTA ACCCTGTAAC TCCCCTGCCT CCAAGAGGTA AGATGCCAAT TTTGGGGAAT 540
TCCTCTTATA CAAAATATGG TGGAAAGAGG GTTTCACAGA TTCAAATCCT GGCTATGATC 600
CCTTCTCGAA TGACCCTGGG TAGGCCTCAC TTTCCTTGTT TCTCCCTATG GAAATGTTAT 660
GAGGACCAAG TAGGAACCAT AGAGTTCTCT GTAAACCTTA AAATGCTACC CAGACAGGAG 720
CAGTAATGGC TGCCAAGGAG CTAGGAAGGA AAAGGGGCTG GACAGGGGCT GAGGTACTCA 780
GATGAAAGCC AAAGATGCCT TGTGTTAACA ACAAAAAGCT GAAAGCTACC TAAAATGAAG 840
AGAAAAATGA ATAAATACAT TGTGGCAATT TCCTATCAGG AAATACTATA CAGCAGTGAA 900
AAAAGAATGA GCCACAGCTG GAGATACGAA CATGAATGAA TCTGGGTCTC ACTCTGTTGC 960
CCAGGCTGGA GTGCAGTGGC ATGATCTCAG TTCACTGCAA CTTCCACCTC CCAGCCCAAG 1020
TCATCCTCCC ACCTTAGCCT CTCAAGTAGC TGGAACTACA GGCATGCGCC ACCACACCCA 1080
GCTAATTTTT GTATTGTTTG CAGAGATGGG TTTTGGCCAT GTTGCCCAAG CTGGTCTCAA 1140
ACTCCTGGGC TCAAGAGATC CACCTGCCTG CTCTGCCTCC CAAAGTGCCA GTAAGGCATG 1200
AGTCACCACG CTCAGCCTAA ATAACATTTT TAAACATAAA AAAATACTAT GTATTATTTA 1260
GGGATGCACA CATTAAAAAA AAAACTTTAA AGAAATGCAA GAAAAAAACC CCACTAAATT 1320
CAGAACACTT GTTTCTTGTT GGTGGCTGAT GAAGGAGAAA TTTCAACTGA TTGGAAATGT 1380
GTTATTTCTT AAACCAGATG AGTGAGCATG TAGGTGCCTG CGTGTTACCC TCGGTATCTG 1440
AGAGACTCCT TCAATTTTTC TTTTTTCTTT TTACTGTATT GTTTGCTTTT TTTCTGCTTC 1500
AACTTTTATT TTAGATTCGG GGGGTACATG TGCAGGTTTG CTACCTGGGT ATACTGCGTG 1560
ATTTGGGTAG GGGTGATCCC ATCACCTGGG TACTGAGCAT AGTTCCCAAC AGTTTTTCAA 1620
CTCTGCCTCC CTCCCTCCCC ACTCTAGCAG TCCCCAGTGT CTACTGTTGC CATCTTTATG 1680
TCCATGAGGA CCTGATATTT AGCTCCACTT ATAAGTGAGA AAATGCAGCA TTTGGTTTTC 1740
TGTTCCTGTG TTAATGTGCT TAGGACAATA TTTTCTAAAA GTCTATGTTG CCAGTTTCCT 1800
GAGGACCAGA TCACGCAGGA GTTGCACCTG CAGAGACAGA AGTGGGCTGG AGAGGGACCA 1860
GGGCTCCTAA GTCTGCTGCT GAAGCTGACT ATAGCGAAGG CAAAGGACAA GTGGCCTGAA 1920
GGCCAACAGA GAGCCTGGCC AATGCTCTGC CCAGTGGGTG GAGACTGAGC CAAAGGCCCT 1980
TGACTCATAG GGCAGTCCCA TACCTGCCCT GGCCTCTCAG CATGACTCCT TGGTGACACA 2040
ACTCCCACAG CACCCACACA CCTACACCCA CCTACCCCAC ACACACACCC CTGCCTGGGC 2100
TGCCCGGTTT GTCCACTGTG TAGGTGCTCA AGGACGCAGA GCTCCTGCCT CTCAAGGAAC 2160
AGCCTCAGGG TGAGGTCCCT GGGAGAGAAG AGTTCAGCTC TGCCCAGAGC AGCCCTCAGA 2220
CAAACAGCCA GCTGCTGCTC ACCAGTCATC CATTCCAATC TGAAGAGTGA CTGTCCTGGG 2280
CCAGTCATGG GAAAATCATC AAGAACTTCC CACAATGGTC ATGGTGGCCG CCAAGGTCTT 2340
TCTCTGGGGG TTGGGAGCTG TGCTCCCCCA CAAAACAAGG GGACCCAGCT GCCCTGTGCC 2400
TTCCTGTGGC AACTCTCTGG AGGATGCCTG GATACCCTCC CTACAGACGG CCAGGGATAG 2460
GAGGGGCAGG CACTGCAGGC ATGTGGGGGC ATAGCAGCAA GAATCTAGGA GGGCAGGCAC 2520
AGCAAGGCCT GGCCCAGAGG GAAACCAGGA GCTGCCAGAG CCAAAGAGAG GGTGACCCAA 2580
TCATTGGTTG TTATAGAGTT TTTAAGACTT GGAAGAGAAT GCCCTGAGAT GCCAGAGAGT 2640
GAAACATTTT CATTCTAAAG CTGGGAAACC AAAGTCGGCA AAGGCGAACA GACGTGCCCA 2700
CAGCCACATG GGACAGCAGT GGCACAGAAG AAATGCACAC CTCGTCCTCT GGTGGCCACT 2760
GTGCACTCTC TTACCACACC ATGCTACTGC TCAACCTCTC CCCCTCCCTC ACAGTGGTCA 2820