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

TagContent
EnhancerAtlas ID
HS176-03789 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr1:223902450-223904620 
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: 39             
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_24051chr1:223902436-223903004Colon_Crypt_2
SE_24051chr1:223903089-223903543Colon_Crypt_2
SE_24051chr1:223903970-223904550Colon_Crypt_2
SE_25230chr1:223902434-223903064Colon_Crypt_3
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_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_67677chr1:223898795-223906601u87
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr1223904365223904567
chr1223903033223903347
chr1223902800223903000
chr1223903000223903425
Enhancer Sequence
GCATTTCTCG AATACCTACT ATATGCTGGG CACAATGCAT ATGGTTTCTG CTTCTGAAGA 60
CTTACTTCTG AGGCTAGTGA GGGGACAGAG ACAGGTCCCC CAACAGTTGG AAATGCCTGT 120
GGGACTTCCA GATGAGGATG TAGAGGTCTA GAGATGATCT AGCGCCACTG CTTAGGGCAG 180
GCGGGCTGTG CACTGCACAA CTAAGGAAGA GTGTGACTTT TACGATCCCC ATTTGCCAGT 240
TGAAGAAATT GAGGCTTGGG AAGGTTAAAT ACTTGCTCAG AGTCAAGTGG ATATAGGGCA 300
TAGATCCAGG ACTGTGTGTA GTCTGTGCAT GTTGAGCCTA CCCCTTATGG CTGCGCTCTC 360
TGCCTCCTTC CTACCTTCTC AAATGCTGCT GAGGTCAGGC AAGGGGAGCA CAGTTGTTTC 420
CGCTGGATTT GAACACTAGC AAGTCATTGG TGAGTTTAGC AGAGCAATTT CAATGGAAAG 480
GTGAGAGTAG AAGCCAGATT GTTGTAGACT CCAGAGTAAA GGAACTGGAA ATTAAGAACA 540
TGATCAACTT ATTTAAGAAG GACCCCCGGG AAGAGAGGAG AACTGATAGG TAGAGTAGGA 600
CCTGGACTTT GAGAGCCTGT GTTTTTTTCA TATGAGAACA ACTTGAATGT GTCATATGTT 660
GAATCACCAG GAAGAAGGGA TTAAAGATAA AGGCAGGGAG GGGGCAGTGA AACAGGATCC 720
CTGAGGAAGT GAGAATACGG GTTGTGGGCA GGGGAGGGGA GCAGGTTAGC CTTGCAGCAG 780
GAGGAGCTGC TCTTCCTCGG AGAGAGGATT TCACAACACT GGCAAGAGTG GCTCCAGTGC 840
CTGGAGCGGG GATTAAAGCA GTAAGTCCAG TGGGGTCCAA GGGCCATGCA GGGGTACAGT 900
GAGGAGAAAG CAGGTGTGAT CCGGGTGGCA CATCAGATCC TTCCAGCAAC CAGTCTGTTA 960
GGAGCAAGGG CAGATGTTGT GAGCCCCTAT GTTTCCCCCA AGAAAATCAA ACCTCTGAGA 1020
GGTTTCTCAC TTGCTTATCT TCAGCTGGCC GAACTCAGCC TCAAACCCAT ATGTCCTGTC 1080
TCCAAGTTCA GTGACTGTTA TCATCAACTT CTTCAACAGT AATAATAATA GATCACATTT 1140
ATGGAGTGCT TGCCAGGGCA TGTTTACATC ATTATCTCAT TTAACACTCA GAACAATCCT 1200
CTGTGGTGGG TGTTTTCATC GTTCCCATTT TGCAGGTGAA AAAACTGAGA CTTCAAAAGG 1260
TTAAGTGACT TCCCAGGGTC CTACGACCTA CATAATAAGT GGCAGAGCCA GGATTCAAAC 1320
CTAGGTTATC AGAATAATGC AGCAAAGCCC AAACCCTCAG CCCCTTTTCA CTGACTGGTA 1380
AGACCCATAT TTAATTCGAT GCCCTACATG CCGTGCACAA GTTTCAGTTT TCTGAAGCAT 1440
CGCTTAGATG CTTAGGTGTT TAGCACCACT CTGAACTCTG ACTTTTCTAG AGAGGCTGCT 1500
AAAGGCATTA GAAAGTTTCT GAAGTATAAT GGAAAAACCC TGCTGGAGTA AGTGCCTGGC 1560
ACACTCAGGA TTATCAGTGT GATTCTTTAT AATAAACAGG CTCCCAGCAC CAAGCCCAAT 1620
CTATTCCATC AGCTGGATAA GAGCTCTCTG GCAGGCCTTG GGCCAAGCTG GCTTCCTTTG 1680
CCTCAGCAGA AGAGCATTCT GATTCTCTCT GCCATCCCCA AAACTGACAG GAGCAGAGAG 1740
AAACAAGGCA GAGGCATGAA GGGAATGTCC TCTGCGGCAG ATGGTGCTTC CGGAAGAGCT 1800
CCCACAATCT GAGCTAGAAT GAACAGGGGC TAGATCCAAG TCTCATATAG GCATACTTCT 1860
GCTTGACAGA GTGGGCATGC CGAGGGCCGT TGGGTGGAGG CAGGCGTGTG CAACCCAAGC 1920
AGACATGAGA CGCAGCTCCT TCAAGGCAAG GTTGCCTGAG CCCAGAGAGG CTCAAATTTG 1980
TGCCCCAACT TCCTCTGTGG CTTTTGGGTG GGGCTCTTCA GAATCGAAAC ACACTCAGAG 2040
GGCTGCTGAA AGGGCTAAGA AGTGTTCAAG GTTGGCTTCC ATCAGGCTGC TCATGACAAT 2100
GGCCCCTGAG GTTTTAACAC CCTTGAACGC TTGGTACTAA ATCAATTAGA GGCAGGGCAG 2160
GAGCAGAAAG 2170