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

TagContent
EnhancerAtlas ID
HS117-00721 
Organism
Homo sapiens 
Tissue/cell
LHCN-M2 
Coordinate
chr1:226890730-226891800 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE41MA0636.1chr1:226891308-226891318GTCACGTGAC+6.02
BHLHE41MA0636.1chr1:226891308-226891318GTCACGTGAC-6.02
USF1MA0093.2chr1:226891307-226891318GGTCACGTGAC-6.14
USF2MA0526.2chr1:226891304-226891320GCCGGTCACGTGACGG+6.15
ZNF263MA0528.1chr1:226891201-226891222CCCCCACCTCCTCTCTCCTCC-6.92
Number of super-enhancer constituents: 47             
IDCoordinateTissue/cell
SE_00103chr1:226889060-226893178Adipose_Nuclei
SE_03159chr1:226890055-226891960Brain_Angular_Gyrus
SE_03869chr1:226889349-226893050Brain_Anterior_Caudate
SE_04801chr1:226888209-226892798Brain_Cingulate_Gyrus
SE_05781chr1:226888049-226892389Brain_Hippocampus_Middle
SE_06710chr1:226889242-226892390Brain_Hippocampus_Middle_150
SE_07746chr1:226888913-226892972Brain_Inferior_Temporal_Lobe
SE_08795chr1:226890597-226891091Brain_Mid_Frontal_Lobe
SE_08795chr1:226891306-226891438Brain_Mid_Frontal_Lobe
SE_08795chr1:226891442-226891626Brain_Mid_Frontal_Lobe
SE_10211chr1:226890007-226892112CD19_Primary
SE_10887chr1:226873819-226893407CD20
SE_11833chr1:226890100-226891304CD3
SE_11833chr1:226891325-226892398CD3
SE_13607chr1:226890004-226892378CD34_Primary_RO01536
SE_14432chr1:226890267-226892206CD4_Memory_Primary_7pool
SE_15456chr1:226890195-226891995CD4_Memory_Primary_8pool
SE_15808chr1:226890297-226892105CD4_Naive_Primary_7pool
SE_16345chr1:226890472-226892567CD4_Naive_Primary_8pool
SE_16856chr1:226890110-226892221CD4p_CD225int_CD127p_Tmem
SE_17296chr1:226887872-226908646CD4p_CD25-_CD45RAp_Naive
SE_17765chr1:226887869-226893077CD4p_CD25-_CD45ROp_Memory
SE_18263chr1:226887975-226903974CD4p_CD25-_Il17-_PMAstim_Th
SE_19160chr1:226890004-226892711CD4p_CD25-_Il17p_PMAstim_Th17
SE_20012chr1:226889957-226892254CD56
SE_21455chr1:226890073-226892303CD8_Naive_7pool
SE_21910chr1:226889098-226892688CD8_Naive_8pool
SE_22315chr1:226889193-226893095CD8_primiary
SE_25774chr1:226888100-226893183Duodenum_Smooth_Muscle
SE_26570chr1:226889267-226891978Esophagus
SE_29606chr1:226889178-226892079Fetal_Muscle
SE_31634chr1:226889239-226891913Gastric
SE_40782chr1:226889189-226891993Left_Ventricle
SE_42228chr1:226889214-226891900Lung
SE_48218chr1:226889290-226891900Psoas_Muscle
SE_48643chr1:226889324-226891854Right_Atrium
SE_50140chr1:226889292-226891914Sigmoid_Colon
SE_51367chr1:226889193-226892316Skeletal_Muscle
SE_52562chr1:226889223-226891918Small_Intestine
SE_53341chr1:226889211-226892093Spleen
SE_54498chr1:226888025-226894921Stomach_Smooth_Muscle
SE_55112chr1:226890147-226891818Thymus
SE_58303chr1:226819953-226937809Ly1
SE_59629chr1:226819233-226928465Ly4
SE_60416chr1:226819368-226929640DHL6
SE_61009chr1:226812849-226900772HBL1
SE_62233chr1:226813614-226929647Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1226890865226891416
Number: 1             
IDChromosomeStartEnd
GH01I226701chr1226888703226892578
Enhancer Sequence
CTGTGTTTCA GCAGCTTAAA CATTGAGGTC TGACAAGAAC CCGAGATTCC ACTTTGCCTG 60
CCAAGGGCTA AGTGTGTATG CTGAAGCGAA AGAAAGTGAT TATGAGGAAA AATGGGGAAT 120
GTCTGAGTGG GTGAAGGAAA AAAAAAGTGC AAGATATTAC TAGAAAAACC TGACTGCACA 180
CACAATCCTA TCCCCTACGC AGGAGAAAGA CCGAGTGCTA GCACCCGGGG TGTGAAAGCC 240
TGCACCAAGG GACCCAGGAA CCAGGCGTGC CTCCATTTCT CACTCGATTT GTTTACAATG 300
AACGGACGGC GCCGGAGTCC CTCCGCCCTC AGCTCAGGCC CGGTTCCCAC CGCCCGACGC 360
TGGCTGGCCG AGGCAGGGGC GCGGCGGGGG ATTTCGGGCA GGGCGGTGAA GCAGGGCCTG 420
CTCTACAGGG GGCTTTTCTT CGCCGCGGTT TCTTCCCCTG TCGCTGCCCG GCCCCCACCT 480
CCTCTCTCCT CCCGCGCGCG CTCTGCCCGC CGCCCACGCG CGGAAGCCCG CGGCCGGGGA 540
GGGGGCGCCG TCTCCCGGCA TGCTCGGCGG CGGTGCCGGT CACGTGACGG GAAGGCGGCC 600
GCCCCTGTCG CCTTCGCCAG CGCTAGCGGG CCCGCAGCAG AGGCAGTAGC GGGGCTTGAA 660
ATGCTGACCT GCACCCCTGG CTTGCGCTCC CCCAGGCGGG AAAGACAAGG GGGCTGCTGT 720
TGCTGCTTAC GAAAAGAATC TCAGCGCTGC TGGCCGCCAG CTTCCGGCTT GGGAGAAAGG 780
ATGTGTTTCA GTCTGGGTTT CCTCATTTGC AAAATGGGTA TACTTTTTGT AGGGTTGAAC 840
TGTAGGTCAG CAGGCTCCCA AATCCTGTCT TTCCTTGTCC CCCTCACCCC CAAGAGTAAC 900
AACTTTTAAT TAATTTTGTT CAAGAGCTAA TAAAAAAAAA ATCTTCATTT CTTTGGATGA 960
CACTGTGCCC AACTCCACGG TCAGCTTGCA GAGCGTAGCG GTTCTGCCCG AAACCCATCC 1020
GCCCAAGGCT TTTATTTTCC TAGATCTCAA ACAGTGGGAG GGTCGGACTC 1070