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

TagContent
EnhancerAtlas ID
HS002-04854 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr19:13960880-13962770 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr19:13961365-13961376GGGGGCGGGGC-6.02
KLF5MA0599.1chr19:13961366-13961376GGGGCGGGGC-6.02
PLAG1MA0163.1chr19:13962168-13962182CCCCCGTTAGCCCC-6.26
PLAG1MA0163.1chr19:13962236-13962250CCCCCTAGGCCCTC-6.32
SP3MA0746.2chr19:13961364-13961377GGGGGGCGGGGCC-6.11
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00394chr19:13948737-13963116Adipose_Nuclei
SE_00791chr19:13961433-13962030Adipose_Tissue
SE_00791chr19:13962168-13962426Adipose_Tissue
SE_02576chr19:13959489-13964991Astrocytes
SE_09068chr19:13961590-13962107Brain_Mid_Frontal_Lobe
SE_13342chr19:13948702-13962977CD34_Primary_RO01536
SE_14690chr19:13956464-13962797CD4_Memory_Primary_7pool
SE_15885chr19:13960875-13961655CD4_Naive_Primary_7pool
SE_17782chr19:13943266-13962691CD4p_CD25-_CD45ROp_Memory
SE_24646chr19:13960770-13962750Colon_Crypt_2
SE_27158chr19:13957065-13962903Esophagus
SE_27768chr19:13949302-13963575Fetal_Intestine
SE_28760chr19:13949189-13965110Fetal_Intestine_Large
SE_29787chr19:13956506-13962940Fetal_Muscle
SE_34630chr19:13946176-13967046HeLa
SE_36667chr19:13959473-13965372HMEC
SE_37011chr19:13948733-13965296HSMMtube
SE_38128chr19:13956463-13965113HUVEC
SE_39105chr19:13961475-13962948IMR90
SE_41122chr19:13956563-13963049Left_Ventricle
SE_42413chr19:13956569-13963420Lung
SE_44426chr19:13956507-13962882NHDF-Ad
SE_45089chr19:13960639-13964642NHLF
SE_46491chr19:13955521-13964784Osteoblasts
SE_49032chr19:13957052-13962760Right_Atrium
SE_49472chr19:13960823-13962773Right_Ventricle
SE_51833chr19:13960791-13963307Skeletal_Muscle_Myoblast
SE_54944chr19:13956487-13963104Stomach_Smooth_Muscle
SE_56033chr19:13960695-13963675u87
SE_58196chr19:13960880-13961346VACO_9m
SE_58196chr19:13961368-13962715VACO_9m
SE_63613chr19:13960696-13963563HSMM
SE_68219chr19:13949152-13977449TC32
SE_68559chr19:13949281-13977291TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191396120013961600
Enhancer Sequence
TAATACACAT AGGCCCACAC ATGCATAGAA CAGGCTTAGA ACATAGAACG TGCTCATTAA 60
GTGTTAGCTA GTTTGGGAGG TCGGCAGGGG TGGGGAGGAT GCAAAAAAGC CCTCATCACA 120
GCGCTCCTGA CAGCTCCCGC CAGGCCAGCT CCCCAAATCC CTTAGGAAAA TGGCCTCGAC 180
CTCTCAGCTG CAACTCTGGC CCAGCCGCCA TCTCCTGACC TGACCGCCCA CTTCTGGGGA 240
GCCCCGGTGG GTCTGGATTG GAGAGAGCCA CCCTCAGCCC TCCCCACCTT CATTGGACCA 300
CAGCTGTCTC CTTCACCATC ACCTCCGTGC CCACCAGGAT TACAGGCCTG ATCTGAACCC 360
CTAATCTAGG GAAGACTACG GAGTCCCAAA ATCCCTCTTA GCGCGCACCC CGGCCTGAGG 420
CTCGAACCCA GGTCCGCGCT GGAGGGCGGT GGCGGTTGCC GAGCAACGCG CTGTTTGTTG 480
GCGCGGGGGG CGGGGCCGGG GCCGGCGCGC GGTGACTCAC CGCGGCGTGA TGCGGACGGG 540
CGCGGCGCCC AGCAGCCTGG CCGGCGGCCC GATCTCGGCT GGCCTCGGCG TCCGGAGGGG 600
CCCGGCGGCG GGGGCGCCTT AGCCCCCAAG TGGGCGCCGG AGGCCCGTGG GGAAGCGGCG 660
GAGCAGGTCC CGGGCTCTCG GACTCGGTTC GAATCCCAGC CCTGCCTCTT ACTCTTGACT 720
CTTGATCTGT GACTTCAAGG CTCCTTGCCT CAGTTTACCC GTCAGTAAAA GAAGCGACAC 780
TGGAGGGTGC AGTAACCCAC CACTGGCATT TAAAGCAGCT GAGATGATCA CGCAGTGACA 840
CTGCGGGGCA GCAAGTTTGG GACACCCAGA TTCTGCACGT GAATCTCCTG TGTTAAACTC 900
TGCAACCTCA CGGAGAATCA ATTTCCGCAT CTGTTACAGG GCAGTAGCAA GAACAAACAC 960
CCTGCCTCTC GGGTGGTTTG AGAATCCCGT GAATTCATAG TGAGACAATG CGTGGCACAT 1020
TTCAGTACCA TGTCTGCTGC CCCACGGAGG GACGGGATGT AGGAGGTTTT CTCTGTGGTC 1080
CGAGCTCAGG AGGGCAAGGA GGTGAGGGCA AGACTGGAAC CCCTAGAAGT GGGTGGCAAG 1140
TCACAGGTCC AGGGCAGGGT GGCATGACCA TGGCTGCAGA GGCCCCTATC CCGAAGCTGG 1200
CTCACAGCAC CTGCTGCGGG CAGGCAGAAG GGGGGCCTGG GGGTGAGTCA CCGCCCAGCA 1260
ATGAGGCTTG AGTCACACAG GGCGGGGTCC CCCGTTAGCC CCCCCAGCTG CTCCCACAAA 1320
GGCCCTTTGA GAAGAGTTCC CCACCCCCTA CTCCCACCCC CTAGGCCCTC TCTAGGGGTG 1380
GGCTGTGGGG CCGAGGCCCT GCTGGGCTGC CCCCAGGAGC CCGGCCTGGG TCTGGGAGGC 1440
GCCAGCCAGT TTCAGCCATG TCTGTGAAAA GTCACCATAG GAAGCTGGGT GTCCCCCGGG 1500
GAGGGGGCTT CCAGGCTGCC TGAGTCACTG GAATGGTGGA GGGTCACACG CGCAGGGCCC 1560
ACGCACACAG CGGGCAAATT GAGTCAGACT GTCTGGTGGG GCGGGCAGGC CAGGACGCTT 1620
CGAGTCAGGC TGAGAAGGAA ACCTGGGAAG AGACATGGTT CTTCCAAGCC TGTGGCCTCT 1680
GGCAGAGAAA GAGGGTGCTT GAGGGCACAT ATGGTGGGTT TCACCACACC TCCTGCCTAG 1740
GCCTCCCCTC CTTGCCTGCC CCGAAACAGT CTCCCCCACC TTTCTATCCT TCTTAAACTT 1800
GGAGTGAGAA GGACAGCAAG CTGGATGGGA TTCCAGGGAG GCACTCTACT AGCGGAAGAA 1860
TTGAGATTTT TTTTTTTAAT TTTATTATTT 1890