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

TagContent
EnhancerAtlas ID
HS174-00332 
Organism
Homo sapiens 
Tissue/cell
SK-MEL-5 
Coordinate
chr1:154399530-154401670 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TCF7L2MA0523.1chr1:154400148-154400162CCCCTTTGATGTCT-6.14
ZNF263MA0528.1chr1:154401281-154401302TGAGGAGGAGAGCGAGGGGAG+6.42
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00437chr1:154399481-154401751Adipose_Nuclei
SE_01040chr1:154399528-154400582Adrenal_Gland
SE_01040chr1:154400681-154401626Adrenal_Gland
SE_06653chr1:154399347-154403450Brain_Hippocampus_Middle
SE_09189chr1:154398672-154408855CD14
SE_16173chr1:154399945-154400671CD4_Naive_Primary_7pool
SE_18405chr1:154399517-154407766CD4p_CD25-_Il17-_PMAstim_Th
SE_19165chr1:154401205-154402489CD4p_CD25-_Il17p_PMAstim_Th17
SE_24531chr1:154399580-154400359Colon_Crypt_2
SE_26130chr1:154399302-154401704Duodenum_Smooth_Muscle
SE_26877chr1:154399516-154400662Esophagus
SE_26877chr1:154400694-154402391Esophagus
SE_32086chr1:154399571-154400607Gastric
SE_32086chr1:154400656-154401897Gastric
SE_41139chr1:154399325-154402156Left_Ventricle
SE_41647chr1:154399531-154400535LNCaP
SE_41647chr1:154400745-154403911LNCaP
SE_42431chr1:154399355-154400656Lung
SE_42431chr1:154400696-154402137Lung
SE_47983chr1:154399591-154400258Pancreas
SE_47983chr1:154400922-154401243Pancreas
SE_48261chr1:154399318-154401864Psoas_Muscle
SE_48934chr1:154399344-154402194Right_Atrium
SE_50453chr1:154399516-154401315Sigmoid_Colon
SE_51380chr1:154399138-154401914Skeletal_Muscle
SE_52880chr1:154399518-154401631Small_Intestine
SE_54618chr1:154399097-154409137Stomach_Smooth_Muscle
SE_62668chr1:154357227-154415486Tonsil
SE_65390chr1:154399323-154400849Pancreatic_islets
SE_65390chr1:154400868-154402476Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1154399696154400530
chr1154399716154400696
chr1154400830154400990
Number: 1             
IDChromosomeStartEnd
GH01I154427chr1154399576154401508
Enhancer Sequence
ATTACAGGAG CCTGCCACCA CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG AGACAGGGTT 60
TCACCATGTT GGCCAGGATG GTCTCGATCT CTTGACTTGT GATCCGTCTC GCCTCGGCCT 120
CCCAAAGTGC TGGGATTACA GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC 180
AGGACAGTAC TGTGTGCTGT GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA 240
AGGGCAGGTC TCTGGGATGC CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC 300
TCCTCAAATG TTTATCAAAC ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT 360
GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA 420
CCCAAGGTCT GTTGGTGACC AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT 480
ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT 540
AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC 600
CAGGCAGAGC TGTCTCCGCC CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT 660
AGCCAGTGTG GACTCCAACC TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA 720
TCCTTACTCC CTCCTCTGAC AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA 780
GTATGAGATA AAAACGCCTC ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG 840
TGCTGCTTCT GAGTCCCAGG AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC 900
TGGTCCTCTC TGAAATCTTT GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG 960
CATTTGGTTC AAAGGACCAA GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG 1020
TTTCCTTAGC TGGTTGGACT AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT 1080
AATTTTTATC TTAGATTCTA TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC 1140
TTTAATCTTT AATCTTATTT TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT 1200
AGAGAATGCA TTTTTTTTTT AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT 1260
GTAGTAGATG TAGGGTACTG GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA 1320
CCCCAGCTGG GCATCTGGGC CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT 1380
AACGGGCATT CTGCCATGAA TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT 1440
GGGTGCCTGG CATTCATTCC TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG 1500
CAGACTCCTG CCATGGGCCA GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG 1560
CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA 1620
ATTACATGGC AGCGTGTGGG TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC 1680
CGGAAACGAT GTTTAGGCCG AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG 1740
AAGAACGAGT GTGAGGAGGA GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG 1800
GAGTGGGGAG AGATGAGGCC TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT 1860
TGGACTTCAT CTTGTGGATG GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG 1920
GTGGCTGGAT CATGGCTTCA GAAGGCTCTC CCAGGCAGCT GGATGGTGAA GACCAGGTTG 1980
GGGAGGTCAC CAGGAGAATG CTGCCCTAAT CCAGGCAGAG GTGACGGTAG CCTGGGCCAC 2040
TTCATCATTA TCACTGAGGC CTCTCGTGGC TTCCTCAGAC CAGAACGAAG CCCCCTTCTT 2100
CAGTGGCTGT GGGCTCACCA AGTGTCTTCT CCCTCCTCCA 2140