EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-13969 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr18:2980730-2982360 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs681869chr182981398hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr18:2981369-2981380GGTGACTCATT+6.02
IRF1MA0050.2chr18:2982321-2982342AAAGAGAATGTGAAACCAAAT-6.72
JUN(var.2)MA0489.1chr18:2981365-2981379GGGAGGTGACTCAT+6.43
Stat6MA0520.1chr18:2981726-2981741TAGTTCCTGAGAACT+7.03
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00574chr18:2976859-2983595Adipose_Nuclei
SE_09781chr18:2978007-2983661CD14
SE_10621chr18:2977964-2983444CD19_Primary
SE_11211chr18:2975484-2985847CD20
SE_11888chr18:2978055-2983488CD3
SE_13797chr18:2979325-2983109CD34_Primary_RO01536
SE_14570chr18:2975646-2983611CD4_Memory_Primary_7pool
SE_15580chr18:2979488-2983763CD4_Memory_Primary_8pool
SE_16149chr18:2978915-2982300CD4_Naive_Primary_7pool
SE_16392chr18:2978239-2983268CD4_Naive_Primary_8pool
SE_16996chr18:2977997-2983215CD4p_CD225int_CD127p_Tmem
SE_17424chr18:2974248-2985971CD4p_CD25-_CD45RAp_Naive
SE_17870chr18:2975509-2984093CD4p_CD25-_CD45ROp_Memory
SE_18346chr18:2974499-2983964CD4p_CD25-_Il17-_PMAstim_Th
SE_19436chr18:2975557-2983449CD4p_CD25-_Il17p_PMAstim_Th17
SE_20084chr18:2975958-2983770CD56
SE_21011chr18:2977827-2983410CD8_Memory_7pool
SE_21798chr18:2978515-2983757CD8_Naive_7pool
SE_22207chr18:2977951-2983581CD8_Naive_8pool
SE_22362chr18:2975903-2983839CD8_primiary
SE_26140chr18:2975618-2986379Duodenum_Smooth_Muscle
SE_28431chr18:2978214-2987374Fetal_Intestine
SE_29294chr18:2979664-2987478Fetal_Intestine_Large
SE_31871chr18:2979663-2981598Gastric
SE_32704chr18:2979488-2983601GM12878
SE_46307chr18:2976888-2983944Osteoblasts
SE_51026chr18:2978269-2981007Sigmoid_Colon
SE_51026chr18:2981029-2981917Sigmoid_Colon
SE_52825chr18:2978085-2981896Small_Intestine
SE_55616chr18:2981101-2981640Thymus
SE_58874chr18:2954099-2995404Ly3
SE_59888chr18:2955879-2985795Ly4
SE_62302chr18:2955378-2999752Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1829812362981736
Enhancer Sequence
TGGAGAAGAG GTCTGGGCTC TGTGCCGGGG GTTCTCTCTA ACAAGAATGG TCAGGTGACC 60
TCTAGAGTCC CCCCCCAGCT CTAAACTGCA GAAAAGCTCC AATTCTATAA GCATTTCTGA 120
GGATTACAAG TTTGGCTAAG AACTCCTGTA GTATATTCTG CCCTAAATGG GGTGAAAATA 180
TGGCCAGTAG ATTATTCTGG GACTTCAGGT TATTTGAATA TAAAATAATT TAGCTTTTTC 240
CTTAGCAAAT AAAGGTATTG TCTTCACTTG TTTCAAAAAA TATGAAAACA TGGTCTTTGA 300
AATTTCCCAA TTTCTAACAA AGCACAGAAA TCTTCTCATG GTTTTCCAAA TCATGATATG 360
ATACATTTAT ATTCCCAAAT CACAAAACCA TGAGGAAAGA CTCTTTCAAA ACTGAAACTG 420
TCACCTTACA AAAGGGGTGC CCAGAAAGGA TGTGATTTGT AAGGAGTGTT CAGGTCACAG 480
AAGGCCTGGA CCCTGAAAAC CAGGGTTCTC CCTCTAACCA CACACACCCA GGTTATAAAG 540
TCAAACTCCT ATATAATCAT TACAGGCTAC TAAGCAGATA TCAGATCCTT ATCCCAAACG 600
TTAGCATTAA GAAAACTCAT GCTTCTCATG GGACAGGGAG GTGACTCATT AGACTTCAAT 660
GTTCTAACGG CAACATAAAA TGGGACCGTT AATAAAATGC AGCCTAAGCA AACACCTCTT 720
GACCTCTTTC TGGAAAACAC CAGCAGACAC AAGTCTTAAG AACTTCCTGT GAGGGAGAGT 780
TTATGTGTGT TAGTGCTACT TAATATATGA ATGTTTAAAG TATTTCGTAA AAAGTCAGCA 840
AGGTTCTCTA TTCTCCCTTC TGACCTTTAC AACAAATGTG AGTGAGCCAA TATGTGTATA 900
CATTCTATAA TATTACAATG TTGATTTCAA AAGCAAACTG CCTCCCCCGT GGTAGCACCT 960
GACTCTTCCA TTCATATTCA AACCACGTCT TTCCATTAGT TCCTGAGAAC TCTGAGTAAG 1020
TACACTTTCA CTAACAGATC CAAAAGCAAA AAGCAGAGTG TGATAACATT TTTAAAGATA 1080
ATAAACATTT GTATAACCTT AAAACTAAAA TCAAGTTATG AGCCACAGAT TTTAGAAACT 1140
AATTTTTGTC TCACTGATTT TATGCTTGTT TTCATAAAAA TATCCATCCT TAATTTTAAA 1200
AAATAACCTT GAAAATAGTG TTTCCTTCCT ATTATTTTTA AAGGAAAGCT TCCACAGGTA 1260
GAGTTACACT GTCCTCAAGT CACTTGATTT TGTTTCTTTA ATGCAGATTT CTGGGACTTA 1320
CACTAAGCTT ACATAACTTG TTCTAAGTTA TATTTTGTAA CAAGAGAGAA AACTCTGGAT 1380
TAAAGAAGTT CATACAATTT ATATTTTCCC CACATACTTC AAGCTTACAA AAATTCTTGT 1440
TTATGATCAC AGAAGAAAGC AACTGCAGCC ACTCTCATAT ATCCAAATAC AACGTCAGCT 1500
TCAAAATATT AGTTTACCAT TCCAAAAATT ATGACTAGGC CAACAAAAAC TGTAACACTT 1560
TTATATGATT TTTACTACTA CACTTAAATG CAAAGAGAAT GTGAAACCAA ATATATTATT 1620
TTTGAAACAT 1630