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

TagContent
EnhancerAtlas ID
HS191-03481 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr1:223903080-223905460 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TP53MA0106.3chr1:223903596-223903614TGCTTGCCAGGGCATGTT+6.17
TP53MA0106.3chr1:223903596-223903614TGCTTGCCAGGGCATGTT-6.32
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00224chr1:223891886-223912166Adipose_Nuclei
SE_01908chr1:223903739-223904850Aorta
SE_02306chr1:223899487-223903687Astrocytes
SE_04026chr1:223903291-223905474Brain_Anterior_Caudate
SE_05036chr1:223902343-223904766Brain_Cingulate_Gyrus
SE_05972chr1:223899184-223905867Brain_Hippocampus_Middle
SE_09681chr1:223899395-223907924CD14
SE_19702chr1:223899422-223907008CD4p_CD25-_Il17p_PMAstim_Th17
SE_23408chr1:223902389-223903605Colon_Crypt_1
SE_23408chr1:223904046-223904670Colon_Crypt_1
SE_23408chr1:223904914-223905971Colon_Crypt_1
SE_24051chr1:223903089-223903543Colon_Crypt_2
SE_24051chr1:223903970-223904550Colon_Crypt_2
SE_26209chr1:223899230-223905388Duodenum_Smooth_Muscle
SE_26925chr1:223899336-223904834Esophagus
SE_31491chr1:223898405-223906097Gastric
SE_33950chr1:223900271-223904290HCC1954
SE_34545chr1:223899419-223904575HCT-116
SE_34979chr1:223899218-223904777HeLa
SE_36294chr1:223899426-223904613HMEC
SE_37129chr1:223899390-223911201HSMMtube
SE_38254chr1:223899363-223904539HUVEC
SE_38957chr1:223902403-223904692IMR90
SE_42269chr1:223902366-223906841Lung
SE_44530chr1:223900206-223905349NHDF-Ad
SE_44904chr1:223902263-223903610NHLF
SE_44904chr1:223903924-223904809NHLF
SE_44904chr1:223904975-223905561NHLF
SE_45872chr1:223899383-223910101Osteoblasts
SE_50365chr1:223899342-223907084Sigmoid_Colon
SE_51879chr1:223902338-223905051Skeletal_Muscle_Myoblast
SE_53249chr1:223902420-223905033Small_Intestine
SE_55958chr1:223898795-223906601u87
SE_63671chr1:223902338-223906710HSMM
SE_64794chr1:223900231-223904926NHEK
SE_65644chr1:223902687-223903954Pancreatic_islets
SE_65644chr1:223904002-223904652Pancreatic_islets
SE_65644chr1:223905019-223905988Pancreatic_islets
SE_67677chr1:223898795-223906601u87
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1223904365223904567
chr1223903915223904781
Enhancer Sequence
TATGAGAACA ACTTGAATGT GTCATATGTT GAATCACCAG GAAGAAGGGA TTAAAGATAA 60
AGGCAGGGAG GGGGCAGTGA AACAGGATCC CTGAGGAAGT GAGAATACGG GTTGTGGGCA 120
GGGGAGGGGA GCAGGTTAGC CTTGCAGCAG GAGGAGCTGC TCTTCCTCGG AGAGAGGATT 180
TCACAACACT GGCAAGAGTG GCTCCAGTGC CTGGAGCGGG GATTAAAGCA GTAAGTCCAG 240
TGGGGTCCAA GGGCCATGCA GGGGTACAGT GAGGAGAAAG CAGGTGTGAT CCGGGTGGCA 300
CATCAGATCC TTCCAGCAAC CAGTCTGTTA GGAGCAAGGG CAGATGTTGT GAGCCCCTAT 360
GTTTCCCCCA AGAAAATCAA ACCTCTGAGA GGTTTCTCAC TTGCTTATCT TCAGCTGGCC 420
GAACTCAGCC TCAAACCCAT ATGTCCTGTC TCCAAGTTCA GTGACTGTTA TCATCAACTT 480
CTTCAACAGT AATAATAATA GATCACATTT ATGGAGTGCT TGCCAGGGCA TGTTTACATC 540
ATTATCTCAT TTAACACTCA GAACAATCCT CTGTGGTGGG TGTTTTCATC GTTCCCATTT 600
TGCAGGTGAA AAAACTGAGA CTTCAAAAGG TTAAGTGACT TCCCAGGGTC CTACGACCTA 660
CATAATAAGT GGCAGAGCCA GGATTCAAAC CTAGGTTATC AGAATAATGC AGCAAAGCCC 720
AAACCCTCAG CCCCTTTTCA CTGACTGGTA AGACCCATAT TTAATTCGAT GCCCTACATG 780
CCGTGCACAA GTTTCAGTTT TCTGAAGCAT CGCTTAGATG CTTAGGTGTT TAGCACCACT 840
CTGAACTCTG ACTTTTCTAG AGAGGCTGCT AAAGGCATTA GAAAGTTTCT GAAGTATAAT 900
GGAAAAACCC TGCTGGAGTA AGTGCCTGGC ACACTCAGGA TTATCAGTGT GATTCTTTAT 960
AATAAACAGG CTCCCAGCAC CAAGCCCAAT CTATTCCATC AGCTGGATAA GAGCTCTCTG 1020
GCAGGCCTTG GGCCAAGCTG GCTTCCTTTG CCTCAGCAGA AGAGCATTCT GATTCTCTCT 1080
GCCATCCCCA AAACTGACAG GAGCAGAGAG AAACAAGGCA GAGGCATGAA GGGAATGTCC 1140
TCTGCGGCAG ATGGTGCTTC CGGAAGAGCT CCCACAATCT GAGCTAGAAT GAACAGGGGC 1200
TAGATCCAAG TCTCATATAG GCATACTTCT GCTTGACAGA GTGGGCATGC CGAGGGCCGT 1260
TGGGTGGAGG CAGGCGTGTG CAACCCAAGC AGACATGAGA CGCAGCTCCT TCAAGGCAAG 1320
GTTGCCTGAG CCCAGAGAGG CTCAAATTTG TGCCCCAACT TCCTCTGTGG CTTTTGGGTG 1380
GGGCTCTTCA GAATCGAAAC ACACTCAGAG GGCTGCTGAA AGGGCTAAGA AGTGTTCAAG 1440
GTTGGCTTCC ATCAGGCTGC TCATGACAAT GGCCCCTGAG GTTTTAACAC CCTTGAACGC 1500
TTGGTACTAA ATCAATTAGA GGCAGGGCAG GAGCAGAAAG AGTTGGCGCA TTTGATCAGT 1560
AAGTTCCAAT GCCAGTGCTG TCTATTATCT GTGAACTGTG TTAACTTTGG ACACGTCACT 1620
TCACCTTTTT GAGCTGTTTC CTCGTCTGTA AAAGGGGGAT AATACCCATT CCATGAGGTA 1680
AAGCTTTGAG CACAGTCTCT GATGTAAGCA GGTACAGAAT ATATAGATGC TGTAAGTTTC 1740
ATGGTCCCAT GGAAGAATTC AAAAGGGTTA GATCCCGCCT GCCCTCAAAA GGGTATGTGT 1800
TAGGAAATCA GAGTAATACC TAAGTAGTAA ATTGCAGAGT CCAGAGACTC TGGGACTCAG 1860
ACTTGAAGGG ATGAGTGAGG ATTGGACTAG GACGACTTCA CGGAGGAGGT GACAATGAGC 1920
CTCAAGGTAT GATGCAATAT GGAAAAGGAG GGAAGAGAGT GGGAAAGGAA GGAATTTCAT 1980
GCAAGCAAAA CAACTTGCAT GCAGTAACAG AGGAGAGAGG ATGCTAACCC AGTGGATAGG 2040
GTGGCTCTAG AGTGTGGATG GTCTCCACGT CTGGCAGAAA AGGCTGGACT TGCTGCTGTG 2100
GCCCCCGGGA CACAGCACAA TGAAGGAGGC TCCAGGCAGT CCAGAGTGTG CAGGGTCCAA 2160
TGCCTGCCCT TCTCAGACAG GACCACCCAT CCACCCATCA GGGCCCAGGG AGCAGGGGTC 2220
AGAAGGACCT CATGACACAG AGTTCTGACT GTGATGACAC ACTTTCCCCA GAGGGGAGGG 2280
GAAGGGGAGA AGGGGTTAGA AGACCCCACT GAGAATGGAG GCATCCTAGC TGCAGAAGCA 2340
CCTGGCTGGT AGGCTAACAG CACTTTGTGG GTCTCGTTCC 2380