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

TagContent
EnhancerAtlas ID
HS134-05192 
Organism
Homo sapiens 
Tissue/cell
Mesendoderm 
Coordinate
chr1:226910570-226912740 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr1:226911530-226911542GATTGTTTTTTT+6.44
Number of super-enhancer constituents: 32             
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_55112chr1:226910349-226911054Thymus
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
TTGAATAGAT CATCCTGGAC AGAAAAGATG CAAACCCCCA GGGGTCAACC CTGCAGGCTA 60
CCTGCTCCCC CTGCCCCCCA CCCATTACAG CTGAAAGGAA GGAGAGAGTT CCATTTCACA 120
CATCCTGTGT GTAGCAGAGT AGAGACCAGG GTTTGGCAGG CAGGATGCCC AGGGCTGTGG 180
TGACGCCAGT CCGTGCTGCT CAGATGGAAC CTGTAGCCAT CCAGCCCGGA TCCTGCATGG 240
GTTCCAGTAG GCCCTCCTGG GACTTGGAAG TGAGCTGGTG TGCTCGGGGT TCATCAGCTC 300
CGTCCAGTCA CCTGACTGGC TTTTCCTTCC ACTCCACCAT CCCAGCCCAG ATGACAAGGG 360
CACAGTATGG CCTTGTGACT TGGGAAGTCC TGGGTAGGTT CTCTGTGGCT CACTTCAAGA 420
GGAGGCCAGG GTGACGCACA GTGTACTTCA GAGACCCCAG AGCCACCTGG ACCTGAGTCC 480
CTGTGAATGG ACACGTGACG GGCCTCACTG GGTGTGCAGT AAGATAAAAC ATCTCCTTAA 540
TCTCAGAGAG AGCCTGTGTT AATAAGCACG TGCCTGGCCT GGCACCAGAT GCGGCACAGA 600
GAAGAGACGA AGACTAATTA AATCACACAC GTCCAGAGAC CTCCTTGGTA AGAAAAGCCA 660
CACCGATACA GAGTAGTGTT GTTCTACACA CACACGTGTG TGTGGGTGTG TGTGTATAGA 720
GAGATATATA TGTATATATT TCATTGGCTC TCTTATGAGC TACAGTGACT CTAAAAGATG 780
CACCAAGAAA GCAGAGGAAC AAGGGGAAGG GAGGGAAGGG ACAGAGGCTT TCACACCCCA 840
AATGCTGGGC ATTTTGTGTC TGGATGACCT CAGCCAGTTT CCACCTACAA AACAGAATAA 900
AAAGAGGCTG GTCCCCAGGG TGTGTAACCT GACACCTCTT GCCGGCAGCT GAATACAGGG 960
GATTGTTTTT TTAAACTTCA AGTTCCAATC CCTAGTAACA AAGTGAGGCC TCTCCTGCAA 1020
CTAAAGAACC TCCCTGGAAA AATAAATCCT GCTGCCTGTT TTGTCATCAT CTTCGACAAT 1080
TAGCTGTACT TGGGACAACG TGACTCGAGC CAATTGGTGA AGGCGATTAG GGCATCCACT 1140
TAAAAACGCT CTTCACAACT GGTGGAGGGG TGTCCTCTAT TCCACCCCTG TTCTGCACCC 1200
GGTACTTGAG CTGCATTATC TCCTTTCATC TTCACAGCAC CCCCTGAGAG AGGCTCATTA 1260
TCCTCATGTT AGAGATGAGG ACACTGAGAC TCAGAGATGT TCAGCCCACG CCAAGGTCTA 1320
GGACAGAGTG AGGGTGTGGG TTCAGGTCTG GCTGGCTCGG GCTCCACACT CCCCAGCAGA 1380
CCATCTTGCT TCTGTGCTCA GCAGAGCAAG CCTCCCCCAG CACACACTTC CTACAAACCT 1440
CAATGTCAAA GAGCTCCCAG ACCCCATGAC TTCTCCTCTT CCAAGGGAAG AAGTCAGCAA 1500
CACTGCCTCA GACACCCTTA TTCACTCTCA CCCAATCAAA GAGAATGGTG GAGGTCGCAG 1560
GTTCGGCATA AAATACTAAC AAATGACACC ACAGCTGCCT CTGAGGTCCA TGCTATTGTA 1620
TCGAGCATTT AGTATGTCCA GACGCTGTGC TAGGCATTTC CCACATTACC TTGTTTAAGG 1680
CTCACAGCCT TAAGGTGGGT ATTATCAGTC ACATTTCACA GATGATGCAA CTGAGGAGCA 1740
GAAAGTTTTC TCTAGGGTCA CACAGATAGG AAGTAACAGA GTTTAGACTC AACCCAGGAC 1800
TACACCTCAG GGTTCTTCCC CTCCCCCTAG AGCTCTTCCA TAGCTAAGAC TCTATAACGT 1860
GTACTAAGCA GAAAAACCCC TGCCGAGCTC TCCTGACCAT GTCCTTCTGG TCAATCGGGG 1920
TCCTCCCGAG AGCATAGCAA CAGTGCAGCT GACTGGGCTC TGCACCGTGC AACTGCTGAG 1980
CATCAATTTG TGCAGAATCC AACGCTCCAA ATCAAGTACT GGGGCAGGGG TGCCCTCTTT 2040
CATTCCAGCC TCCGTGAGCC TCTGGATCCA GAACAGTCTC TTTGATCTAC CACTTCTAAC 2100
AGAGGGAGCA AATTCCTCAA GACCTTTACC CCAGACTCCT TCCCTAGAGG CTGTTGCCCA 2160
AATCCAGTTC 2170