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

TagContent
EnhancerAtlas ID
HS081-09570 
Organism
Homo sapiens 
Tissue/cell
HACAT 
Coordinate
chr19:13961020-13962690 
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
CAGGCCAGCT CCCCAAATCC CTTAGGAAAA TGGCCTCGAC CTCTCAGCTG CAACTCTGGC 60
CCAGCCGCCA TCTCCTGACC TGACCGCCCA CTTCTGGGGA GCCCCGGTGG GTCTGGATTG 120
GAGAGAGCCA CCCTCAGCCC TCCCCACCTT CATTGGACCA CAGCTGTCTC CTTCACCATC 180
ACCTCCGTGC CCACCAGGAT TACAGGCCTG ATCTGAACCC CTAATCTAGG GAAGACTACG 240
GAGTCCCAAA ATCCCTCTTA GCGCGCACCC CGGCCTGAGG CTCGAACCCA GGTCCGCGCT 300
GGAGGGCGGT GGCGGTTGCC GAGCAACGCG CTGTTTGTTG GCGCGGGGGG CGGGGCCGGG 360
GCCGGCGCGC GGTGACTCAC CGCGGCGTGA TGCGGACGGG CGCGGCGCCC AGCAGCCTGG 420
CCGGCGGCCC GATCTCGGCT GGCCTCGGCG TCCGGAGGGG CCCGGCGGCG GGGGCGCCTT 480
AGCCCCCAAG TGGGCGCCGG AGGCCCGTGG GGAAGCGGCG GAGCAGGTCC CGGGCTCTCG 540
GACTCGGTTC GAATCCCAGC CCTGCCTCTT ACTCTTGACT CTTGATCTGT GACTTCAAGG 600
CTCCTTGCCT CAGTTTACCC GTCAGTAAAA GAAGCGACAC TGGAGGGTGC AGTAACCCAC 660
CACTGGCATT TAAAGCAGCT GAGATGATCA CGCAGTGACA CTGCGGGGCA GCAAGTTTGG 720
GACACCCAGA TTCTGCACGT GAATCTCCTG TGTTAAACTC TGCAACCTCA CGGAGAATCA 780
ATTTCCGCAT CTGTTACAGG GCAGTAGCAA GAACAAACAC CCTGCCTCTC GGGTGGTTTG 840
AGAATCCCGT GAATTCATAG TGAGACAATG CGTGGCACAT TTCAGTACCA TGTCTGCTGC 900
CCCACGGAGG GACGGGATGT AGGAGGTTTT CTCTGTGGTC CGAGCTCAGG AGGGCAAGGA 960
GGTGAGGGCA AGACTGGAAC CCCTAGAAGT GGGTGGCAAG TCACAGGTCC AGGGCAGGGT 1020
GGCATGACCA TGGCTGCAGA GGCCCCTATC CCGAAGCTGG CTCACAGCAC CTGCTGCGGG 1080
CAGGCAGAAG GGGGGCCTGG GGGTGAGTCA CCGCCCAGCA ATGAGGCTTG AGTCACACAG 1140
GGCGGGGTCC CCCGTTAGCC CCCCCAGCTG CTCCCACAAA GGCCCTTTGA GAAGAGTTCC 1200
CCACCCCCTA CTCCCACCCC CTAGGCCCTC TCTAGGGGTG GGCTGTGGGG CCGAGGCCCT 1260
GCTGGGCTGC CCCCAGGAGC CCGGCCTGGG TCTGGGAGGC GCCAGCCAGT TTCAGCCATG 1320
TCTGTGAAAA GTCACCATAG GAAGCTGGGT GTCCCCCGGG GAGGGGGCTT CCAGGCTGCC 1380
TGAGTCACTG GAATGGTGGA GGGTCACACG CGCAGGGCCC ACGCACACAG CGGGCAAATT 1440
GAGTCAGACT GTCTGGTGGG GCGGGCAGGC CAGGACGCTT CGAGTCAGGC TGAGAAGGAA 1500
ACCTGGGAAG AGACATGGTT CTTCCAAGCC TGTGGCCTCT GGCAGAGAAA GAGGGTGCTT 1560
GAGGGCACAT ATGGTGGGTT TCACCACACC TCCTGCCTAG GCCTCCCCTC CTTGCCTGCC 1620
CCGAAACAGT CTCCCCCACC TTTCTATCCT TCTTAAACTT GGAGTGAGAA 1670