EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS003-20183 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr17:48928180-48931210 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF8MA0652.1chr17:48929673-48929687ATGAAACTGAAACT+6.74
IRF9MA0653.1chr17:48929672-48929687CATGAAACTGAAACT+6.08
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_03575chr17:48928899-48930318Brain_Angular_Gyrus
SE_04376chr17:48928756-48930814Brain_Anterior_Caudate
SE_05363chr17:48928823-48930884Brain_Cingulate_Gyrus
SE_06228chr17:48928535-48930847Brain_Hippocampus_Middle
SE_07101chr17:48928769-48930603Brain_Hippocampus_Middle_150
SE_08443chr17:48928655-48930948Brain_Inferior_Temporal_Lobe
SE_14970chr17:48928884-48930241CD4_Memory_Primary_7pool
SE_16087chr17:48929248-48930006CD4_Naive_Primary_7pool
SE_20704chr17:48929029-48930225CD56
SE_21303chr17:48929048-48930438CD8_Memory_7pool
SE_23284chr17:48928158-48928567Colon_Crypt_1
SE_23284chr17:48928937-48930250Colon_Crypt_1
SE_23284chr17:48930393-48930915Colon_Crypt_1
SE_23884chr17:48928918-48929352Colon_Crypt_2
SE_23884chr17:48929371-48930263Colon_Crypt_2
SE_24759chr17:48928914-48930027Colon_Crypt_3
SE_24759chr17:48930038-48930430Colon_Crypt_3
SE_26239chr17:48928752-48931159Duodenum_Smooth_Muscle
SE_27071chr17:48928781-48930217Esophagus
SE_27621chr17:48929304-48931280Fetal_Intestine
SE_28540chr17:48929334-48931122Fetal_Intestine_Large
SE_29895chr17:48929332-48930422Fetal_Muscle
SE_31700chr17:48928933-48931542Gastric
SE_35249chr17:48928521-48930452HeLa
SE_36764chr17:48928908-48930336HMEC
SE_41204chr17:48928045-48931001Left_Ventricle
SE_42705chr17:48928749-48931024Lung
SE_47770chr17:48929551-48929923Pancreas
SE_48377chr17:48927898-48931648Psoas_Muscle
SE_49138chr17:48928733-48930879Right_Atrium
SE_50682chr17:48928846-48931013Sigmoid_Colon
SE_51175chr17:48927008-48936168Skeletal_Muscle
SE_52750chr17:48928936-48930959Small_Intestine
SE_53677chr17:48928866-48930373Spleen
SE_63033chr17:48928840-48949433Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174892972748930800
Number: 1             
IDChromosomeStartEnd
GH17I050850chr174892812948931348
Enhancer Sequence
CGCATGTGTG ATATTTTCCA CCACAGATTC AAGAACAGTC AAGTCTGGTT TCGTCTCATT 60
TTTGTGTCCT CCCTTCTCCC TGCTAATATA CCAGGAAGTT TTACTTCCTA GGATTCTCAT 120
GAAAAGGCAC GTTTATAGCC AGCTGACCTC CCCTAAATAG GCTGAGCACA TGCCCTTGAG 180
GCTAAGCCGT GCGGGGAGAG GTGGAGGATT TGAGCCCTCT CTCACCACAG AGTAAAGAGA 240
GTGCAGGTTA TTCTATGTAG GGAAGAGGAT TATGCTGAAT GCTTTATTTA TCTTACATGC 300
TCATCACACC AACCCTAACA AGTAGAATTT GGAACCCTTT TACAGTTAGG AAATCTGAGG 360
TGGAATCGTT TTAACAGTGC ACTGCTATTT AAGGTTGAGT TTGAGATTTG ATTCAAAGTC 420
TGACCCCAGG CCAGGCGTGG TGGCTCACAC CTGTAATCCC AGCATTTTGG GAGGCCGAGG 480
CAGCGGATCA CCTGAGGTCT GAAGTTTGAG ACCAGCCTGG CCAATATGGT GAAACCCCGT 540
CTCTACTAAA AATACAAAAA AATTAGCCGG GCTTGGGGCT GGGCACCTGT AATCCCAGCT 600
ACTCAGGAGG CTGAGGTAGG AGAATCCCTT CAACTCAGGA AGCAGAGGTT GCAGTGAGCC 660
GATATTGCGC CACTGCACTC CGGCCTGGGT GATAGAGCAA GACTCTGTCT CAGAAAAAAA 720
AAAAAAAGGA AAAAAAAAAG TCTGACCCCA AAGCCCACGT TCTTTCTCAT AGAGGATCAC 780
GAGGAGTAAT GTTATTTGGA GGCTGAATGA AGCCCCCTAC ACCACTCTAG AGCATTCTTA 840
CATCTGCAGG GGAAATTGTG GGGCCTAAAC ATGTGTCCCC GCTGGTCAAG TGAGTGTGAG 900
ACAAGGATCA GACGCTGGTG TCTTCTGTGC CAAAGCAGGA TCCACACTCT GTACAGAATA 960
GTGATGCTCT CTGAACAGTC CCAGGTCACA TGAAGGAGTT TGGCCAGCTT GTGGTGGTAT 1020
TTTCAGTGGA TGACAGAGTG CTCAGCCACC AAGAGAACTT AGGGAAGCCT GGGGAAGGGC 1080
ATTGCCCGGG GAAGTGACCC AGGCGAAAAG TTATTTGGGA ATGTTAATTT CTGGCTGAAA 1140
TTTATACAAA GCTTTCCCTT CAAAGCCTCA TTCTTTGATT TATGTTCAAA CCGGAAGATA 1200
TTACAAGCAC CCAAAAAGCC AAACTGGAAA AGGAAACTGC AGAGCTCCAC AGACTTGTTG 1260
CCTTGGCCAG GGGTAGGGTG TGGCGATGGG AGTGGCAACT GGGAGTGACC TGGGGGTGTC 1320
TGAGTTTGTG CAATGAACAC GCACTTTCCA CCAACACCAA CTTCTGGAGG GGTAGTACCT 1380
GCTGTGAGCC CTGACATCAC AAAACCAAAA GAGGCTTTGT CACTAAAGGT AGGAAAACAA 1440
ATGAGATGAC CCCTAGAGGG AGCTTCTAGC CTGAGGAAGT TTCTAGATTA AGCATGAAAC 1500
TGAAACTGTC TTAAAAGGAA GGAATTCGAC ATCCCTCTGA CACAGCCTGA CGCCCCTCTC 1560
AGTCCCACCT TTTCTTTCCT TGGACTTCTT ACTGGTCCTC CCCATCTCAC TCCTGGGTTT 1620
GATGAATAAA GAAGTTTTAA ACTATTTCTC TTTCATAATG TTTCTGTACA AAGCTTGAAA 1680
CAGTGAAAAA ATAAGTTAAA ATGTTCAAAT TCAAAGGCAG GTTCTCCCAG GAGAGATGGG 1740
CTGGCAGCAG AGCTTCTATT TCTGATTTCC TCTGCCTTTT TCCCCAAGGG TTAGCAGCAC 1800
ACATTCTTCC TACTGTGGCT ACATCTGATG AAGAACACAC ACACACACAC ACACACACAC 1860
ACACACACAC ACACACCAGG ACCAAGGTTT TCCTCTCAAC TGCCTGTTCC TCCACTGGAG 1920
CTGGGAATTT GAGGGAGCCC AGGCTTCCCC GGGTGCTTCC AGTGGACATT GTACCCATTC 1980
TTCATAGCTG GATATCTCCC CCCAGATCTA GCATCCCTAA GATAGGCACA GTCTCACCCT 2040
TTTTTGTTCA TACCCCTACA TTTTCCTGTG TATTATGATT ATTTGGGCGT GTGTGTTATC 2100
GTTTGCTAGA ATGTAAGCTC CTTTAGAGGT TCCGAAGGAT TGTATATATC ACTGCCAGTT 2160
CCTAACGCAG GAGATGCTTA ATAAATGTGT TGAGTGGATG AATACAGGAG CTGTTTTTAA 2220
TCATATCTCA CCTTGTTTGA GAAAGAATTT AGGGACAAGA ATGGAATCTG AGCCCAGGGC 2280
AGCCACTTGA GTCAACATCA CCCTTTTGCT ATCACAAGTA CTAGTAAAGC TCAGGACCCA 2340
AGACTTCAGT ATGTGAAGTG CCTATAGTTG CTTCTCAACA AATCTAATCA TCCAGAGAGC 2400
AGTCGCAATG TAAGTAAGTA AAGCTAGCAC GTAGCCCTCA AACTCATATC TTACTCCATT 2460
GTGTTTTTGC AACCGATTTC CCTTTCCTAA TTGTGCCTGG CAAAGGCTGA TAGCAAAATA 2520
AGTTTGGGAT TGCTGAGCAA ACAATCACAA GTGAGGTTTG CAGGAGAGGG GGACTGGGCA 2580
CAAAGTGCAG CTTAGATGAC TTCTAAATAA TCAGGTGGGG CTCTTTTTAT AAAATCGACC 2640
GGTTGAGGTC AACCAAGGGA GCAGGATAGT GTAATGGTTA AGGATCATGG ACTTTGGAAA 2700
CAGAATCCCA CAGTTCAAAT CCTAGCTCCG CTGGCTGTGA CTGTTGCAAG CTCTCTGCCT 2760
CCACTTATAT ATCTGTAAAT GGGAGAAACA GTACAACCTT CAGAGGGTTG TTATGAAGTT 2820
GAACTGAATT TAAATGGGGC AGTATCTAGC ACATAGTAAA TTCATATAAG GGTTGCCATT 2880
ATTACTACTG AGCTTTTGGG GTTGGTCATT CCCTCTGGAT TCCATAAGAC TTTGTGATAG 2940
TATAAAAATC ATCCTTCAAA TAGGCAGTGC TTTACGTAGG AGCAGTTCCC CATCCTCCTT 3000
GAAAATCTGG GAAAAAAACA CGCGCACAAT 3030