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

TagContent
EnhancerAtlas ID
HS034-02739 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr1:226911200-226911900 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr1:226911530-226911542GATTGTTTTTTT+6.44
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00103chr1:226910268-226914123Adipose_Nuclei
SE_03869chr1:226909642-226914235Brain_Anterior_Caudate
SE_04801chr1:226909769-226913572Brain_Cingulate_Gyrus
SE_05781chr1:226909371-226914464Brain_Hippocampus_Middle
SE_06710chr1:226909842-226916981Brain_Hippocampus_Middle_150
SE_07746chr1:226909997-226913021Brain_Inferior_Temporal_Lobe
SE_10887chr1:226909951-226923692CD20
SE_11833chr1:226909764-226911682CD3
SE_14432chr1:226909851-226912708CD4_Memory_Primary_7pool
SE_16856chr1:226911061-226912520CD4p_CD225int_CD127p_Tmem
SE_17296chr1:226909602-226929357CD4p_CD25-_CD45RAp_Naive
SE_17765chr1:226909495-226928628CD4p_CD25-_CD45ROp_Memory
SE_18263chr1:226909481-226929370CD4p_CD25-_Il17-_PMAstim_Th
SE_19160chr1:226909740-226917128CD4p_CD25-_Il17p_PMAstim_Th17
SE_20012chr1:226910259-226912653CD56
SE_21455chr1:226909788-226913136CD8_Naive_7pool
SE_21910chr1:226909778-226912096CD8_Naive_8pool
SE_22315chr1:226909647-226920088CD8_primiary
SE_25774chr1:226910377-226912751Duodenum_Smooth_Muscle
SE_26570chr1:226910465-226912445Esophagus
SE_31634chr1:226911457-226912281Gastric
SE_40782chr1:226909759-226913910Left_Ventricle
SE_42228chr1:226911370-226913154Lung
SE_48643chr1:226911574-226912796Right_Atrium
SE_50140chr1:226909756-226911426Sigmoid_Colon
SE_53341chr1:226910761-226911343Spleen
SE_54498chr1:226909687-226917100Stomach_Smooth_Muscle
SE_58303chr1:226819953-226937809Ly1
SE_59629chr1:226819233-226928465Ly4
SE_60416chr1:226819368-226929640DHL6
SE_62233chr1:226813614-226929647Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1226911425226911742
Number: 1             
IDChromosomeStartEnd
GH01I226722chr1226910218226912514
Enhancer Sequence
GTCCAGAGAC CTCCTTGGTA AGAAAAGCCA CACCGATACA GAGTAGTGTT GTTCTACACA 60
CACACGTGTG TGTGGGTGTG TGTGTATAGA GAGATATATA TGTATATATT TCATTGGCTC 120
TCTTATGAGC TACAGTGACT CTAAAAGATG CACCAAGAAA GCAGAGGAAC AAGGGGAAGG 180
GAGGGAAGGG ACAGAGGCTT TCACACCCCA AATGCTGGGC ATTTTGTGTC TGGATGACCT 240
CAGCCAGTTT CCACCTACAA AACAGAATAA AAAGAGGCTG GTCCCCAGGG TGTGTAACCT 300
GACACCTCTT GCCGGCAGCT GAATACAGGG GATTGTTTTT TTAAACTTCA AGTTCCAATC 360
CCTAGTAACA AAGTGAGGCC TCTCCTGCAA CTAAAGAACC TCCCTGGAAA AATAAATCCT 420
GCTGCCTGTT TTGTCATCAT CTTCGACAAT TAGCTGTACT TGGGACAACG TGACTCGAGC 480
CAATTGGTGA AGGCGATTAG GGCATCCACT TAAAAACGCT CTTCACAACT GGTGGAGGGG 540
TGTCCTCTAT TCCACCCCTG TTCTGCACCC GGTACTTGAG CTGCATTATC TCCTTTCATC 600
TTCACAGCAC CCCCTGAGAG AGGCTCATTA TCCTCATGTT AGAGATGAGG ACACTGAGAC 660
TCAGAGATGT TCAGCCCACG CCAAGGTCTA GGACAGAGTG 700