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

TagContent
EnhancerAtlas ID
HS091-02979 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr1:154398920-154401670 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs34172480chr1154399397hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:154399000-154399021AAAAAAAAAAAGAAAGAAAAG-6.41
POU2F2MA0507.1chr1:154399204-154399217TGAATTTGCATGT+6.05
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
CAGGAGGTTG AGGATGCAGT GAGCCGAGAT CGCGCCATTG CACTCCAGCC TGGGTGATAG 60
AGCGAGATTC TGTCTCAAAA AAAAAAAAAA AGAAAGAAAA GAGAAAAGCA TATCACAGCA 120
GAAGACTATA TTCAAACCAT TTATATGAAG CTCAAAAATG AAGCAAAGTT AAGAAAAATG 180
TAGGGATGTA TGGGTAGTGA AAGTTAGGTT GGTGGGCTTT CCTGGGTATT TTATGCTTCA 240
TAAATTAACT TTTATGTATG TAGCTTTTAC ATACATTATA TATATGAATT TGCATGTATT 300
CAGTATTATG TAATACATTA AAAACAATGT TCGCAATGCT AAAAATATAT TGTTGAAGAT 360
TCTGTGTGAA AGCTATACTG TAGTTGTGGC TTTTTATAAC CCTTTCAAGC CCTCTGGGCA 420
GTAGCAGTCC ACCCCTTATT GCCCTCAGTG GACTTCACCT TCTAGGGACT CAGAATTTTT 480
TTTTTTTTTT TGAGACGGAG CTTCGCTCTT TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT 540
CTCGGCTCAC TGCAAGCTCC GCCTCCCTGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA 600
AGTAGCTGGG ATTACAGGAG CCTGCCACCA CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG 660
AGACAGGGTT TCACCATGTT GGCCAGGATG GTCTCGATCT CTTGACTTGT GATCCGTCTC 720
GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGGC CCAGCTGGGA CTCAGATTTT 780
GCTGAGGACC AGGACAGTAC TGTGTGCTGT GTCCTGGCCT TGCAGCAGTG AATGTGTCTC 840
CCGTTTCTCA AGGGCAGGTC TCTGGGATGC CTGACTGTGT CTTCCTTGCC AGTGCCTGGC 900
TGCTGCAGCC TCCTCAAATG TTTATCAAAC ACAGGACTTG CCCACCGTGG GAGAAAGTAA 960
GGCCATAGGT GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC TGCACGGTGA CAATTCAACC 1020
AGCTTTCTTA CCCAAGGTCT GTTGGTGACC AGAGAAAACC TTAGATGACC GGCTGCCATG 1080
ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA 1140
CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG GTATCTGTAT AGCTAGACAG 1200
GGCTCAATGC CAGGCAGAGC TGTCTCCGCC CCTTTGATGT CTATGTCTCT GTCCCTGGAC 1260
TGTGGCCAGT AGCCAGTGTG GACTCCAACC TCACCAGCTT TAGGGGTGTT ATCTGCCTGG 1320
GAGTCACTGA TCCTTACTCC CTCCTCTGAC AGCCACCTTG GATGGGGTGA AAGGAAGGAC 1380
AGCCTGCCAA GTATGAGATA AAAACGCCTC ATAAACAAGA AGGGATTTGC AGGCCAGGCA 1440
GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG AGCATGGGCG AGGAGGTGAG GTCAGGCACT 1500
CAGCAGCTGC TGGTCCTCTC TGAAATCTTT GGCCAGATTT ATTGCTACTG CTTGCTAATA 1560
AATGGTTATG CATTTGGTTC AAAGGACCAA GTGTGCTTAC ATGAAAACTG GCTGTGTTCC 1620
CTGGCCTCTG TTTCCTTAGC TGGTTGGACT AATTTGATTG GTTAATAAAT GAGTCCAAGG 1680
TGGTTGGGCT AATTTTTATC TTAGATTCTA TGACTCTATA ACTGCTACTC AAAAAAAGTG 1740
TACTTGTTCC TTTAATCTTT AATCTTATTT TTCTTGAGTA GTAGAATACA CCCAATTTTT 1800
TTCAAGGGGT AGAGAATGCA TTTTTTTTTT AACCTTCCAG TTTGGTCCCT AGAGTAAACA 1860
CAGCATTGCT GTAGTAGATG TAGGGTACTG GAGGGAGCAT GGAACAGGGA ACCAGAAGCC 1920
CTGGTTCCTA CCCCAGCTGG GCATCTGGGC CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA 1980
CCAACTATAT AACGGGCATT CTGCCATGAA TACCCTGCGA TTTGGAAACC TCCTGTGTAC 2040
GTGTGCACTT GGGTGCCTGG CATTCATTCC TAATGGCATC CATTCGTTCA CACATTCATC 2100
CAGTACTCAG CAGACTCCTG CCATGGGCCA GGCAACGTCC CGGGCACTTG GAATATAATG 2160
GAGAACAAAG CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT CTTGAGGGGA AGAGAGACAC 2220
GGAATTCGTA ATTACATGGC AGCGTGTGGG TGACGTATTG CAGAATGAGG GCCTAGTGGA 2280
GCTGGGGGAC CGGAAACGAT GTTTAGGCCG AGACCTGGAA TAGGAGGAGT TGTCGTGGGG 2340
ATGATGTAGG AAGAACGAGT GTGAGGAGGA GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC 2400
ACCTTCTAAG GAGTGGGGAG AGATGAGGCC TCCAAGGACA GAAGGGCCCT GCAGGCCACG 2460
CTGAGGAGCT TGGACTTCAT CTTGTGGATG GTGGCAGGCC CTTGAAGGGT TTTCTAATCC 2520
AGGGAGTGGG GTGGCTGGAT CATGGCTTCA GAAGGCTCTC CCAGGCAGCT GGATGGTGAA 2580
GACCAGGTTG GGGAGGTCAC CAGGAGAATG CTGCCCTAAT CCAGGCAGAG GTGACGGTAG 2640
CCTGGGCCAC TTCATCATTA TCACTGAGGC CTCTCGTGGC TTCCTCAGAC CAGAACGAAG 2700
CCCCCTTCTT CAGTGGCTGT GGGCTCACCA AGTGTCTTCT CCCTCCTCCA 2750