EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-13301 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:73683740-73686010 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SOX10MA0442.2chr17:73685565-73685576TGCTTTGTTTT-6.02
SPI1MA0080.4chr17:73685165-73685179TACTTCCTCTTTCC-6.51
SPICMA0687.1chr17:73685165-73685179TACTTCCTCTTTCC-6.91
ZNF263MA0528.1chr17:73683781-73683802CTCCCCACCTTCTCCTGCCCC-6.26
ZNF263MA0528.1chr17:73684262-73684283GGTGCAGAAAGGGGAGGAAGA+6.52
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_03279chr17:73683982-73685223Brain_Angular_Gyrus
SE_03279chr17:73685354-73686038Brain_Angular_Gyrus
SE_04001chr17:73682465-73705208Brain_Anterior_Caudate
SE_05218chr17:73683487-73704230Brain_Cingulate_Gyrus
SE_06028chr17:73679436-73705327Brain_Hippocampus_Middle
SE_07212chr17:73682397-73698116Brain_Hippocampus_Middle_150
SE_08211chr17:73682578-73702695Brain_Inferior_Temporal_Lobe
SE_23597chr17:73684055-73684650Colon_Crypt_1
SE_24278chr17:73684079-73684616Colon_Crypt_2
SE_26294chr17:73683489-73686041Duodenum_Smooth_Muscle
SE_26940chr17:73683620-73687341Esophagus
SE_28154chr17:73683929-73684707Fetal_Intestine
SE_31090chr17:73682484-73690062Fetal_Thymus
SE_31632chr17:73683706-73685738Gastric
SE_33907chr17:73683601-73687045HCC1954
SE_34296chr17:73683666-73684693HCT-116
SE_34660chr17:73683810-73686071HeLa
SE_35907chr17:73679249-73694632HMEC
SE_38365chr17:73679204-73691897HUVEC
SE_41082chr17:73683616-73685924Left_Ventricle
SE_42678chr17:73683523-73686080Lung
SE_49201chr17:73683603-73685243Right_Atrium
SE_50776chr17:73683659-73686106Sigmoid_Colon
SE_52592chr17:73683710-73686039Small_Intestine
SE_53680chr17:73683550-73686129Spleen
SE_55482chr17:73683668-73688641Thymus
SE_56442chr17:73684070-73685371u87
SE_56442chr17:73685734-73692981u87
SE_59560chr17:73656917-73686758Ly3
SE_64300chr17:73679247-73688655NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177368550073685825
Number: 1             
IDChromosomeStartEnd
GH17I075683chr177367912573698792
Enhancer Sequence
ATTGGGTTTG AAATTTTTTT GTAATTCAGC GTTGGTGTCC CCTCCCCACC TTCTCCTGCC 60
CCTTGGCAGA CTTTTATTGC AAGCCTAGCC CTTTTGTTAG CTGCTCTTCT GCTGCCTGTC 120
CGTCTGACAT TTCTAGTGAA TCTACACATG AAACTCACTG TGGAGTTGAC CAGGCTGGGA 180
GTCTGAAGTT AAAACATAAC AGCTGAAGGT AGGTGTGGAA CCTAAACTTG ACAGAAGACA 240
AACTGACAGT GTTTGGGGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGAGAG 300
AGACAGAGAG AGGTCAGTGC TTGAGCACCT TCTGTGGACC AGGCTGACTA TTAGACTTGG 360
TGATTTTTGT GAGTACACAG AGTAGAGTAG TTTGTCTTCA TCGGCCAGGT GAGCATGAGG 420
GTAGAGGAAG GCTTCCCTGG GCTGGGCTGA GGCCTACACG GGGCTTTCTA GGCAGGAGTG 480
GGGAGAAGGT GATTTCAGGG AGCAGGCATT GCAAAGATCC TGGGTGCAGA AAGGGGAGGA 540
AGAGGCTGAA ATGGGCAGCA GGGAATCCTC AAGGCTCGTG GGCCACAGTG AGGATCTGTT 600
TTTAAGGAGC TATTGTGCTC GTGAAGTGAG ATCTCATCAG GCCATGGGCT GTCCCAGGTC 660
TGAGAGAATA AAGGTTTGAA AGGAGTCATT TTACTAATCT GCCTCCCTAG CTGCCACGTA 720
CTTGTAAGAT GCAAGATTAC ATTGCCCAAC AGGAAACCCC CAGTCTGTAG CATTCTTGCC 780
TGTGGCCTCG GGGCTGGCTG CCCTGTGCCC CTGTTCAGAG TGCTTTCTCT GTGCCCGCTA 840
CTCCCGAAGC TGGAAAGAAA ACATGACGTT TAGATTTGGT GGGATCTAGA TGCTGGCGGC 900
TGCCTTTGTG GAACTCAAGT TTGACACTGG AGCTTTGTGG GGCCGGTTCC AGGAAGGATT 960
GAGGAAGCAT TGTTGGCTGT AAATAAACCT CCATTCTCTT ACTCAGGACT TGGTACTTCT 1020
CTGCTGAGTA AATCCTCCCA GCTCAAATGG CAGCTTGTCC AGTTTCGTGG GTCTATATTG 1080
TTGTTACTTC CTTCCTGCGC TCCAGTCAGC TTCATCAATG GCTGGACTTT TGTATTCTCT 1140
GCAGGAGGAA CCATATTCCA GGTTCTGTAA TTCTTGAGAA CCAGGCCCCT GCCACTGACC 1200
TACAGTTGCA TCTTCCAAGT CTCAGTCACA GTTGGTTAAG AAACCAAATT GGCAGGTTGA 1260
GATCACTATT CTTCTCCAGG GACAGCGCCC AGTGTGCCGC AGCCGCCTCC TGCTCTGGTT 1320
GTTGGGCCTT TAGTCTCAGG TGGGGTCTGG GTGGATGAGG GGTGCAGGCA GAGGAGGAGA 1380
CCTCGGCTCA GATTGGTGTC CTCCACCAGC TCAGCGTTTA AACCATACTT CCTCTTTCCT 1440
CCTTTCTGTT TTCTAACTTG GCTTTTGTTT TTGTCTTTTC GTTTTTCCTT GTATCTTTTT 1500
TTTTTTTTTT TGGAGACAAT CTTGCTCTTT CAGGCTGGAG TGCAGTGGCG CAATCTCGGC 1560
TCACTGCAAC CTCCACCTCT CAAGTAGCTG GGATTACAGG CATGCACCAC CATGCCCGGC 1620
TAATTTTTGT ATTTTTAGTG GAGAGGAGGT TTTACCATGT TGTCCAGGCT GGTCCCAAAC 1680
TCCTGGCCTC AAGTGATCTG CGCACCTCAG CCTCCCAACT CCCCCAGCCT GTTTTTCCTT 1740
GTGTCTTGAT TGGAATTGAA TGAGGGGGCT GAAGAGGTGG GCCTAGTCTT TTCTCCCAGG 1800
AGCAGCCTTC CTTTCCTAGG TGAGGTGCTT TGTTTTCACC TTCCTTAGGA ACTGGGTGAA 1860
AAGCCCTCAG CCTGTTCTGG CTGTGTGTTG TTGCTCATGT CTCTGGGCTG CGGGTTCCAT 1920
GCCCTCTGGC TGATGTAGAC AGATGCCTGG TGACTAGACA TCCAGGATGA GCTCATTACT 1980
TTAACCAACT GAGAATTTCT ACCTGAAGGC CAGTGGGTGG ATTCATACGA GTCAAGACAG 2040
GTGTTTCCTG TGCATTTCAA AACGCTGCTG GCGGGGAAGA GATGAACAGT GCTTTCTTGT 2100
TGCTTTTTGC TTGTATCCTC ACAGCCCTTC TTTCCGCTTC CTGCCTCTTT AAGGGCATAG 2160
TGAGAATCTC CCCCAGAGCA GGTGGTTTAA CACCAGTGCC TTGAACGACT GGCAGTTTAA 2220
TAATCGAGCC TTTCTTCCGT CTCCTTAATT CTGTCATTTA AAATATTTCA 2270