EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS133-18377 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr2:240204040-240207860 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs62182100chr2240205496hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr2:240206822-240206837CAGGTTCAAAGTTCA+6.53
HNF4GMA0484.1chr2:240206829-240206844AAAGTTCAAAGTTCA+7.73
Hnf4aMA0114.3chr2:240206830-240206846AAGTTCAAAGTTCAAA+6.49
Hnf4aMA0114.3chr2:240206823-240206839AGGTTCAAAGTTCAAA+6.77
RxraMA0512.2chr2:240206830-240206844AAGTTCAAAGTTCA+6.4
RxraMA0512.2chr2:240206823-240206837AGGTTCAAAGTTCA+6.55
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_03965chr2:240206626-240207790Brain_Anterior_Caudate
SE_04828chr2:240205577-240207702Brain_Cingulate_Gyrus
SE_05792chr2:240205365-240208125Brain_Hippocampus_Middle
SE_07753chr2:240206314-240207964Brain_Inferior_Temporal_Lobe
SE_09164chr2:240204579-240205488CD14
SE_09164chr2:240206237-240208014CD14
SE_14931chr2:240206623-240207766CD4_Memory_Primary_7pool
SE_19756chr2:240206585-240207802CD4p_CD25-_Il17p_PMAstim_Th17
SE_24090chr2:240206020-240206584Colon_Crypt_2
SE_24090chr2:240206722-240207721Colon_Crypt_2
SE_25334chr2:240204532-240205612DND41
SE_25334chr2:240205718-240216866DND41
SE_30961chr2:240206722-240207723Fetal_Thymus
SE_34281chr2:240204713-240205414HCT-116
SE_39363chr2:240206729-240208302Jurkat
SE_42224chr2:240206592-240207776Lung
SE_48049chr2:240206114-240207872Psoas_Muscle
SE_50196chr2:240206639-240207804Sigmoid_Colon
SE_52573chr2:240206574-240207771Small_Intestine
SE_53377chr2:240206618-240207697Spleen
SE_54492chr2:240206727-240208017Stomach_Smooth_Muscle
SE_61583chr2:240173973-240272304Toledo
SE_65310chr2:240204765-240207853Pancreatic_islets
SE_66243chr2:240206729-240208302Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr2240206600240207713
chr2240207243240207370
Number: 2             
IDChromosomeStartEnd
GH02I239282chr2240204533240205612
GH02I239284chr2240206496240209391
Enhancer Sequence
CACACAATGT ACACACCACT CTACAATGCA CACACCACTC TCCACACAAT GTACACACCA 60
CTCTACAATG TACACACCAC TCTACAATGT ACACAGCACT CTCAATGTAC ATACCACTCT 120
CAATGTACAC ACCACTCTAC ACACAATGAA CATACCACTC TACAATGTAC ACACCACTCT 180
CAATGTACAC ACCACTCTCA ATGTACACAC CACTCTACAC ACAATGAACA CACCACTCTA 240
CAATGTACAC ACCACTCTGC AAACAATGTA CACACCACTC GACAATGTAC ACACCACTCT 300
ACAAACAATG TACACCCCAC TCTACAATGT ACACACCACT CTACAATGTA CACACCACTC 360
TGCAAACAAT GTACACACCA CTCTACAATG AACACAGCAC TCTACACACA ATGTACACAC 420
CACTCTACAA TGTACACACC CCTCTACACA CAATGTACAC ACCACTCTAC ACACAATGTA 480
CACACCACTC TACAATGTAC ATACCACTCT ACAATGTACA CACCACTCTC CATGTACATA 540
CCACTCTACA ATGAACACAC CACTCTACAC ACAATGTACA CACCACTCTG CAAACAATGT 600
ACACACCACT CTACAATGTA CACACCACTC TCAATGTACG TACCACTCTA CAATGTACAT 660
ACCACTCTAC ACACAATGTA CACACCACTC TACAAACAAT GTACACACCA CTCCACAAAC 720
AAAACATGTG ATGTTCCAGG ATTCGCTCGC CCACAGTCAG CCACGCATGC AGGAGCAATG 780
CTGAGGCTGA GGGTGCAGAG GGAGCTTGAC AGTCAGTGGA AGAATGCGCT CTACAAGAGG 840
ACACCACGGG CCTGGCCCGC AGAGGACTAT GAGGGCAGGG GCTGGCGAGT CAAGCTGGCT 900
GGAAAGGCCT CTCTGAGGAA CTGAGGCTTA AGCTAAAAAA ACTCTGCATG ACGCTGGGTC 960
TCTGAGATCC GGAGGAAGGG GCTCCCGGCA GCAGAAGTGC CCAGGGTGCG GGCCTGAGGT 1020
ACAGGAGCTG CGGGGCTCCT CAAACAGCAG AAAGCCTGGT CTCATGGCTA CCGCCCCCCA 1080
TGAGCAGGAT CAGTGCCGAC GAGGCTGCAG CGAGTGTCGG GCTGGCCACC GCGAGGGGCC 1140
TGGGACGCCA CTGCCGGCAG AGGCTAGAAG GGGCCTGACC ACACCTGGGC GTTTCCACCA 1200
TAAGAACACA AAAGCCCTGC GAGCAGAGAA GAGAGCACTG CAGTACAGAA ATCAGGAAGG 1260
CAGAGTTGTA AGCACTGATT GCATTTGTTT TAATGTGACT TATTTAGTCG TAAGTTTAGC 1320
TAATTTCGTT TTCATAACGG CTGTGTTTGG CAACCCACTT CCGCGAGCGG TAACAGCAGT 1380
GCCGGCCACC ACGGGCGGTC ATGGAATTGG AGAGGATCAG GCGGCCTTGA TGGCGTTTTG 1440
GTGGAAGCAC TGTCACAAAG GGATGATGGG CAGGCTGTCG GGAGTTAGGA GAAGAAAAGC 1500
AAAATACATT TGCTAGCTTC TGGCTTGAAT GCCTGGGCTG ACTGGAGGGG CCATGTAGTG 1560
CCGGGGAGAA GTGGAGAGCA GTTCCAACAT TGCTGGGGGA CAGTAGTGCT GCCTCGGGAT 1620
CTACAGCGGT GAGGCCCCGA AGCGCCAAGG GCGTCGGCGC AGGGGCCCCC AGCCAGTCAC 1680
AGTTCCCGCT TCTGCACCCC AGGGCCTCTG AAAACTGTGA AGTCCATGCT GCGGTCTCCA 1740
CGCCCAGTGG CTTTCCACGT CTCTCCACAT GACACTCACC TGCTGCCCAT CACAGGCCGC 1800
AGACACACTG AGAGGAGCCC AAGTGGTGTC TGAAGCAGGA CTCTCCACCA GGACAGTGCC 1860
GGTCCTGAGC CCAGCTACAG GGAGCCGACC ACAGCGGAGC CGAGGACACC GATGGCAGGA 1920
CTGGCTGCGC TTCTGATGAA TGTGGTTTGG GATGCTGGGT GAGGGACAGA GGGAGCGGGC 1980
CAGGGAGTGG GCAGAGTGAG CCAACGCATG GGGGCAGCCC TGAGCCACTG TGCTGACCCA 2040
GTGATGGCCA ACAGCATGCT CCATCACGGG GACCCTCCGC GGGGCCTCGG GGAGCATCGC 2100
AGAGCTGCCT CCCTGAGGAA TGGGGGCAGG TGCATTGTGG CCCTCGTAGT CAGGGGTGAC 2160
CCTGAGAGCA GCTTCCACAC ACGCCAGGTG ACATGCATGA AAGCCCATCA GGTGCCCCTG 2220
GGCATCCGGT GCCAACAGAG GCAGAGGCAG GTGAAAGGCA AGATGCCCCT GCATGAAGAT 2280
GGTCCCAGCA CACACAGAGC AGGCCACCAC AGTAGGGACT GGGTGGGAGG TGGGGCCTCC 2340
AGGATCTGCA GGGGGAAAGG CACCAGACGG TGAGCGCCCA CGCCCCAGAG CCAGAGGCCC 2400
TTCCACTCTC CAGTGTCCTG GAGACCAGTG TCCCGGTTCA AAAGTAAATA CACAAGCAGC 2460
CCTCCCACAG GAAGCTGAGG AGAGTCTGGG CTGCAGACTG GGGAGACCCA GGATCGGGAA 2520
ACTTTTGTTT CATTGTGTTT TTTAATGTAA GTAATTAGGG TATATTTAGA GGCTCAGAAA 2580
GGAAGCCAGA GACAAGTGAC AAAACTTACA AGGAAAATGA GAGGATATTC ACAATGAAAG 2640
GAGAGATGGG ATCAAAAGCA TGAAGGAAGC CCAGAGACAA GTCGTCTAAA TGCATCCATC 2700
AGTCTACCAA GCCATCAAAT AAAATACATC CCACCCCACA CCTAGACAAT CTACAGTCTA 2760
CCTTCATGGC AACCTGGAAG GCCAGGTTCA AAGTTCAAAG TTCAAAGACT GCAGATGGTA 2820
CAGAGAAAGC GTTACACAGT GAGAAAACAG GCAGCTGGAT GAGCACAGAG CCACGGTGGA 2880
GGGGGACAGA GCCACGCTAA GGAGGAACAC AGCCATGCTG GGGGTGGGAG GGGCAGATCC 2940
CTGCTGGGAG TGGAGAACGC GCCGCGGCTG GGCCCCCAAG TTCGCGGCTG TGCAGCGTGG 3000
CCAGAATGCT GAGCCGGTGC TCTTCCCTGG CATCCTGCAC TTCCTGGGTA AGGAAGGAGA 3060
AGCCTTACAG CAAGGGGTTC CACCGAGGCT GGGGCTTCGC TAGTGTGCGG GGAGGCAGAG 3120
GAGCAGTGCC GGCTGCCAGC AAGTGTCTCC GCCGCGGGAC CTGTCATCCC AGCTGGTGGG 3180
GAGAAAACGA AGCTGGGTAA AAGGGGCTGA GAGAAAGCTG GCCAAAGGTT GGGCTTTTGA 3240
AGTACTAGAA ACTTCCTCTT CTGGGGACGT GGCAGACAAG TCATCTTACA GGCTCTTGTG 3300
CTGTGGAAAC CCCAGGTTCT GCATAAGACA TACCTTCTGT CACACTGCTG GGCTCACCAG 3360
CAGTAAGGAA ACCCTCCAAC AAGCCAGAAA TATATAATTA AGGGAAACAA AAGCAACTCG 3420
AGCTGACAGG AGAGTTGAGG GCAGCGGGTG GAGGACTGCA TGGGGGTCAG GACCGAGGTG 3480
AGCCCAGAGC TGCAGCGTTC AGGATGCAGG GGCTGGAGTC CAGGGCAGCT CCCAGGAAAT 3540
GCACGTGGCA TGCCTATCAG AAGAACGGCC TCCTCACTCC CATCCCTCTA TTTCCAAACA 3600
GTAAGACCAG CGAGACATAC GCTCCCAAGC AAACACAAGC CAACACAGAA AGAAGTGAAA 3660
AAAGGCAGCA AACACATCAA AAGACAGTCA AGTTCTTCAG TTACTCATAT CATGAGAAAT 3720
GGTACGATTA CTGTTTCTGA AACTTTCAAA GAATCTCTTA ATGCTTTATT CACTATCATT 3780
TTCCCCATGT ATGTTTTGAT TAAATAAAAA GTTTATGAAA 3820