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

TagContent
EnhancerAtlas ID
HS176-24892 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr22:20884310-20887270 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SCRT2MA0744.1chr22:20887034-20887047GAACCTGTTGCTT-6.05
ZNF263MA0528.1chr22:20885784-20885805CCCTCCTCCCCTGTCTGCTTC-6.29
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00966chr22:20884213-20888664Adrenal_Gland
SE_02445chr22:20884202-20887715Astrocytes
SE_04597chr22:20884247-20888793Brain_Anterior_Caudate
SE_05425chr22:20884074-20889496Brain_Cingulate_Gyrus
SE_06221chr22:20884152-20889170Brain_Hippocampus_Middle
SE_08018chr22:20884223-20888924Brain_Inferior_Temporal_Lobe
SE_13928chr22:20885105-20886372CD34_Primary_RO01536
SE_13928chr22:20886451-20887561CD34_Primary_RO01536
SE_14430chr22:20884158-20888539CD4_Memory_Primary_7pool
SE_18628chr22:20884008-20885073CD4p_CD25-_Il17-_PMAstim_Th
SE_18628chr22:20886593-20888717CD4p_CD25-_Il17-_PMAstim_Th
SE_20611chr22:20886832-20888656CD56
SE_20981chr22:20884412-20886102CD8_Memory_7pool
SE_22532chr22:20885296-20889341CD8_primiary
SE_27539chr22:20884200-20888380Esophagus
SE_36027chr22:20883870-20888724HMEC
SE_36960chr22:20884007-20888930HSMMtube
SE_40040chr22:20885269-20887408K562
SE_41024chr22:20884335-20888779Left_Ventricle
SE_44170chr22:20884169-20888629NHDF-Ad
SE_45006chr22:20884087-20887544NHLF
SE_45715chr22:20884031-20888900Osteoblasts
SE_48421chr22:20884187-20888477Psoas_Muscle
SE_48978chr22:20884629-20888814Right_Atrium
SE_51756chr22:20884311-20888314Skeletal_Muscle_Myoblast
SE_53780chr22:20884411-20888598Spleen
SE_56041chr22:20884017-20888695u87
SE_63544chr22:20884311-20888342HSMM
SE_64517chr22:20883873-20888702NHEK
SE_65524chr22:20884548-20887712Pancreatic_islets
SE_67959chr22:20884017-20888695u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr222088463920886906
Number: 1             
IDChromosomeStartEnd
GH22I020529chr222088346420889824
Enhancer Sequence
CAAATCTTTT TTTTAATATG GGAAAATCTT TTTTCCTTTA TAGTGTCTGC TTCTGGTGAC 60
ATGCTTAGGA AACCATCATC CTGATATTGT ATAACTCTCC TTCTGTTGTC TTGTGGTCCT 120
CTGTGATTTA GGTTTTTAAA CACATAGGGT AAAGGGTCCC ACATACAAGC TGTGGGCTCC 180
TGTCCCAGGT GGGCAAGCAG GCTGCACACA CAGGCAGCAA TTTACTGGGA GGCTTCTTGG 240
GTGGGGTGAA GTGGAGCTGC CAAAAATTTA TTCTGCCCTA TGAGAGTTCA CTTGATTGAT 300
AGATGTTGTG TTTCTCAAAA TTAGAAAATT AGAAGAAACT CACAGAAGTT TCCTTCGAGC 360
AGAACATAAA TCGGCTGAGA GGAATCATCC TGCCCCCCTG AGGTCAGGAG GGTGAATCTG 420
TGCCCCAGGG AGGAACGCAC CTTCCTGCTT TAGACACCAG CAGAGGACAG AGAAGCTGGC 480
TGTCCTGGGA ATTCATGCCC TCATTCAGCA ATGGGAAAGC AGTTGGACCA GGGAAGGGGG 540
CCTGGCAGTG TGGCAGGGGG AGCAGTGGTA AAGAGGGTGG GGTCAGGGGA GAGGCCTCAC 600
TGAGAGGGGA GAGGGTCCTT GGTGGGAACC AGGGCGGTTG TGGAAGGAAG AGTCAGGGCG 660
TGGAGCAGAG CAGAGCGGGA GTTGGGGTGG GGAGGCCAGT TCATGCCTCA TCAACATGCC 720
TGTGTGAGTG TCCTTCTTGC GGGCGGTGGA GCTGGCCTCA GGGTACACTG CAGGTGACTC 780
AGAGCTCCAA TGGGAGGGTG GCTCTGCCTG AGGGAGCTGC ACATGCTCAT TGGGCCATCG 840
TCTGCTGAGG AGGGGGCAAC AATAACCTCA ACACATGGCG GAGGTGTTTT GGGATGCATC 900
CTATTGCACA TTTGGGCAGG TTGTTGCCTG ACTTATTTCT TTAACGCATA CCTAGCACTT 960
CCTGTATGTC CAGTGCCTTA TAATATTAAC TACTATCATC CTCAGGGCTA CCCGTGAGGT 1020
CGGCACTGTC CCCACCCTTT GTGCAAAGGA AGGATAGGGA GGCGCTGCCA GATGGGTTGA 1080
GGGCAGACCG GGGCAGCTTG CCTCAGGCCT CCCTGGCCTT AGCAGGCTTT AAGTTTGATG 1140
CCCTGTGCTC CTTCCCTAGG AAGCTCAGTT TGCCAGTTTT TTGCTTTATC TTAGTCTCAT 1200
TCAGATTACA AGGACTGGGA CTGGACTCCT GTTGCCAGTT TCTCAATTTG GAATAGGAAG 1260
GAGGTGAGGA ACAACAGGCC CATGCTGGGC AGAAGCCCTG CAGACCAGGC CAACAGTGGG 1320
CCTCTCCTCA CTGCCTGGCC CTGTCTGTGC ACCTTCGTCC TGGCCACAGC CTCTCAGAGC 1380
CCCTCCTTTA TGAAGAGGTT ACGCTTTAGG GGAGGGAGTG CCTCTCCCAA GACCCAGAGC 1440
TGGTGAGTGG CTAGGTTGGA ATTTGAGCCC AGGTCCCTCC TCCCCTGTCT GCTTCCTGCC 1500
AGGCCCAGCT GCCTGCCCCA GCACACGCCT TCTCCCAGGC ACCCTGGCCT CCACTGCCAG 1560
GACGTGCCTG TTTGAGGCCT GGATTCCCCC ATGGCTGCCA CGCTGATTCT CCGTTCTGCA 1620
CGTCGTGTCC CATCAAAATG CATGACAGTA CCACTCCTTG TGTTAAAAAG AGCCAGTTAT 1680
TGTGCCTGGC AGTGATGACT GCCCACTGCA CACAAAAGTG GACGCCGTTG TCTCTGCTCT 1740
CAGGGTGTTC TTAGTATAGT GGGGCTGGCA CACAGAAACC AGAGATTCCT CCAGGAAGTG 1800
CCACAGACAT GGGTGAGGTG GCTACAGGGT TTCTGTGCAG CCGACAGCAG GGGTGCCTGG 1860
GTGGAAGCAG GGTGGGAGGC CCTAACAGGC CTGATGGGAT AGTCAGGCAA TGTGCCAGGT 1920
AGTAGGTCAT CATCCCTGGG GCCCTGGGGA GAGTGTGTGG GGCAGGCGCA GGAGCAGGCT 1980
CCTCAGTGGG CTCCTGGACA GGCTGCCTGC TCTGCTGGTG AGGAGCGAGG CTCAAAGCAA 2040
GCAGGGGCCT GGGTTGCTTC CCACACTCAG TGGCAGTTGC TCACTGGCAG TCATGTGACC 2100
TGGGGAGCTG GCGAGGGCGT GGGGGTAGGA ATGGGAACGG GAGACAGAGG CCCTTTGGGA 2160
GGAATTGCCA CAGATGCAGT GGGAGTTGGG GCAAAGATTT GAACTTTGGA GAATTAAAGG 2220
TGGCAGTCAG AAAGTGAAGG GAGTTCCCAA GTTTCTGGGA TGGGCACTTG GTGCTGGGAG 2280
ATGAAGACAC GAAGAGCTTT TCTTGATGTA TCCCTGCTGG CTGCTCAGGC AGGGTCGGGC 2340
AATGCCATTA AGACACACTG TGTTCTGGGA ACAGTTCTGG ACAGTAAGGA CATCCTCAGA 2400
CCCCTTAGTG GGGGAGCTCC AAGGGCCTGT AATGATGAAT CGGTCCCCTG GGAGGCTTCA 2460
GTCTAAGCTA GATACCAGTT GAACCCTGAC TGAGTACACA GACATAGCTA TGGCAACCAG 2520
CTAGACCATG GCCAAAGGCA GAGCATTGGA GCCCAGTTCA CAGCAAGGGA CTGTGTGCTC 2580
TGAGCCGGTA ACAGTCCTTG TGTTCAGAGG TCTGGCTGGT CGCAACCAGG GAGTGGCCCC 2640
CAGCCCCCTT CCTCAGCTAG AGCGAGCACC ACCCAGGCAG CCTTGGGTTC TTTGGTGGCC 2700
GCCTCATAGG CCTGTACTGT TTGTGAACCT GTTGCTTATG TTGGACAGGA CTGTGGCAGG 2760
ACAGCCATCA AGGGTCTTCC CTTGTGAGCT GACACCAGTC TGCTCTTTGT CCTCCTCTGG 2820
CTGGACAGGC CCTCGTCTTC CCGGCTTGCT TGTGTGGGGG AAGAGCTCAC TGTGACATGT 2880
GGGTTCTCTG TTCTTTGTCT CAGGCTGTGC TCCTTACTCC ATGTTGGGGG CTGTCTCCTT 2940
GTGTGATAGT TTCCTTTCAT 2960