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

TagContent
EnhancerAtlas ID
HS176-10510 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr12:111882030-111884550 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr12:111882363-111882376AGCAGCTGTTGCT+6.59
PLAG1MA0163.1chr12:111883832-111883846GGGGCCCAGTGGGG+6.36
ZNF263MA0528.1chr12:111882477-111882498CTCCCCTCTCACCCATCCCCC-6.17
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00313chr12:111877184-111889811Adipose_Nuclei
SE_01105chr12:111882374-111885128Adrenal_Gland
SE_03792chr12:111882112-111882730Brain_Angular_Gyrus
SE_03792chr12:111882777-111884396Brain_Angular_Gyrus
SE_06099chr12:111881910-111889732Brain_Hippocampus_Middle
SE_08462chr12:111882037-111889880Brain_Inferior_Temporal_Lobe
SE_09337chr12:111861899-111889874CD14
SE_11164chr12:111877342-111885335CD20
SE_11924chr12:111881996-111883985CD3
SE_13643chr12:111879661-111884327CD34_Primary_RO01536
SE_14612chr12:111881982-111884743CD4_Memory_Primary_7pool
SE_15617chr12:111882237-111883985CD4_Memory_Primary_8pool
SE_16453chr12:111881793-111883917CD4_Naive_Primary_8pool
SE_17009chr12:111881890-111884352CD4p_CD225int_CD127p_Tmem
SE_17538chr12:111879408-111885017CD4p_CD25-_CD45RAp_Naive
SE_17816chr12:111879397-111885095CD4p_CD25-_CD45ROp_Memory
SE_18496chr12:111878855-111885074CD4p_CD25-_Il17-_PMAstim_Th
SE_19231chr12:111879894-111884513CD4p_CD25-_Il17p_PMAstim_Th17
SE_20028chr12:111881146-111884553CD56
SE_21344chr12:111881937-111883925CD8_Memory_7pool
SE_22364chr12:111881633-111884909CD8_primiary
SE_24616chr12:111882262-111885111Colon_Crypt_2
SE_32074chr12:111882081-111884569Gastric
SE_38040chr12:111879609-111885412HUVEC
SE_40792chr12:111877378-111887912Left_Ventricle
SE_42263chr12:111881886-111887837Lung
SE_46057chr12:111881866-111884857Osteoblasts
SE_47422chr12:111880472-111884943Panc1
SE_48851chr12:111882225-111887877Right_Atrium
SE_50268chr12:111881894-111887773Sigmoid_Colon
SE_52677chr12:111881995-111885302Small_Intestine
SE_53326chr12:111877253-111887851Spleen
SE_62745chr12:111834432-111886877Tonsil
SE_68830chr12:111882255-111885010H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12111882042111883715
Enhancer Sequence
GGATAAAAGA ACTATAACAT CTGGGATAAA GTTAGCTGTT GAAATAAATA CAAGTCCTAC 60
CGTTGGGGTA GTGTCAGAGC TGGCCTACGT CTTTGACTTT GAGATTCCTA GCAGCCAGAG 120
CAAAGAAAGA AATAGATTAT TCCCACTGGA GCCACAGTGG CCATAACAAA CAGAAGCCAT 180
CTGTTTAGAT GCTGGGAATG GAGAAGACTT GCTCCCCAGA AATAGACGCT GCAGGATGTG 240
GTGGGTGACA GTCTACTGTT CAAACCACAA ATACCTGAAA TGATCTGGCC ACTTTGATCA 300
CCCAACCACA GTAGAGCCTA AGCAGGTCCA GGGAGCAGCT GTTGCTGGCC TGGCTTGACT 360
TTTGAGGGAG GTGGAATAGC GGGCATGTGA GAGGAGGGAA CCTAAAGCCC CCACAGCTGC 420
TGACACAGCC CCCAGGTTTG AGCTTGTCTC CCCTCTCACC CATCCCCCCA TATAGCTTAA 480
TCTGATGGGC ATCTGGTGGT CCTTCCCTGC AGTGGCCAGA GCCTGAGCTG TCCAGGCTGA 540
GGTTTCGACT GAAGCAGGGG TTGTCCTGCG CCCATGTGCC CACACGCTGC AACCTGGCTG 600
GAGCCTCTGG CATAGGACAC CCATACCACC AGGTAGCTGT GGCGGACCCC GGCTCTGATA 660
CTTGGCAGGC TTGGGTTGAG ATTGTGGCTC TAGGCCTGGG CGGCTCTCAA GGGCTGCTGT 720
GGGGAGTTGG GGAAGAACCC CTGGGTTGTG CTCAGCCAGC AGGCAGGTGG CAGCCAGGCT 780
GGCTGTGGGT GAGGAGGGGA ATCCTCTTTT CACCACTGCC TGCCTGCTCA GCAGTTCTTC 840
AGCTGCTGGG GGTGGAGCTG GCTTGCAGGG GCCAGAGTCA GAGTGAAACC GGCAGCTCTG 900
CTGGTTAATC TCAGCACTGA CACTGGGGAC TAGGCCTGGA GCGGAACTGA AAGGGAGACT 960
AGGCCCGTTC CCCTCCAGGC CTGGCCTATA TCCTCCCAGT GATCCTTAAG GCCTGCAGCT 1020
AGGGGGAAGG GTGGGGGCCA GGCAGGGCCA ACTGGAAAAG TAGCAGAAGG AAGTGGCCAC 1080
TCGCACCTTA CCCATCTTGC AGACAGGAAA TGAAGGCTCT GCAGGGCTGG CTGGCTGTAA 1140
AAATGGGCAA GAGCGCAGAG GCCCCACTCC CTGCACACTG CGCTGTGTCC AGTGCCCGTG 1200
TGGATGCCAT GTGAGGCCTC ACTCTGCCTG CCTCATCCTG GCTGCTGGAC CTCTGGGAGT 1260
AGGAGGTGAA AATGCCCTGG CTGGTGCTGG TCACTTCAGG CTGGAATTTT CTAGTCATGC 1320
AGCTTTCTAG TGAGAGGCCG CAGTGAGCTG TGGCCAGTGT TGGTCATTCC TGCAGTCATT 1380
ACTCTCCCCC AGCCTGTTGT GTCCGCCAAC CAGAGCAGGC CCGGGAGCTC CCAGGAGACC 1440
TGCTGGAAGG GCCCAGGTGG CCATCCTGCT CCTGCCAGGC TGCCCTCTTA CCTCACTGTT 1500
CATTGACTCT CCTGCAGGTG GGGAAGGGGG ATAAAGGAGG TGGCCAGGCC ACTGGGTCAT 1560
GATCCTTCCG ACAGAGGTAC CTGGCAGCTC TGTGTGTAAA GCAAGGTTAA GCATCTGGTT 1620
TTGGGGGTCA ATTCAACAGC ACTAGCAGCT CCAGTCCAAG GTATGCCCTT TTGGGCTGAG 1680
GTGGAGGTCA GATCACCTGA AGCCACAGTT GCTAGAACAT CCTTTGGGCT GCCTCTGCTT 1740
TCCATCCCCC TGCTCCCAGT TTGTTAGGGG TTGTAGTATT TTCCAGGAAC ACCTGAATGG 1800
AGGGGGCCCA GTGGGGCCAC TTCTGTCCAT TCCTTATCTC ATCTCTTTCT CCCCTTTTCT 1860
TCTTTCGGCC ATCTTTTCAG TCTTATCACA AGAGGAAGGG GAGGGGCAAA CCCCCTCCTG 1920
AGCAGATTCC CAACCGGAAG CAGCTGGCTC CTTGGCTGCA GAGTGCCCCA GCACAGGAAG 1980
CATCTGCAGG GTCAGTTGAG ACCTGGGAGC AGGTTTCCTG CTGGCAAAGG AACAGTGGCT 2040
AACTCCTATC CACCCTGCAG CCCTATGTGC CGGGTGTCCT GGGAAGGTCC AGGGCCAAGA 2100
TTTTGTGGTT TTACAGTGGC TATAACTTAG GCTAGCCATG CTAGGCTCTG CCCCTTTGGG 2160
CTTGGTGTGA TGAGACCGTC AGCAGCTGCT ATCACCTGGC TGGGCAGGGA GCTGTTTGCT 2220
CACCAGTGGG AAGAGAAACG GATGTCAGAC ACATGGCAGA GTGGGAATGT CTCCAAGTCC 2280
AGGTCCAATG GGCTGGGAGG GCTGGCCTTC TGCCAGCACA TGCTTCTTGG GATCTCAGTG 2340
TGAATGGTGT TCAGGAGGCT AGGGGAAGGC ACCCTGGACC TCACTACAGG CTCAGAGCCT 2400
GCCCAGCAAC ACCATGGATA CTCTCTCTAA AAGGGGGACT CCTGGGGAGA CTATAGACAA 2460
ACTCAGGCCT GGCTGGAAGA AAGAGCATCA GGAACAAGCC TTGAGTACCC CAACTTGGTC 2520