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

TagContent
EnhancerAtlas ID
HS113-02389 
Organism
Homo sapiens 
Tissue/cell
Keratinocyte 
Coordinate
chr1:154398830-154401670 
Target genes
Number: 8             
NameEnsembl ID
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
ACAAAAAAAG GAAAAAATTA GCCGGGCATG GTGGTGTGTG CCTGTAGTCC CAACTACTCG 60
GGAGGCTGAG ACAGGAGAAT TGCTTGAACC CAGGAGGTTG AGGATGCAGT GAGCCGAGAT 120
CGCGCCATTG CACTCCAGCC TGGGTGATAG AGCGAGATTC TGTCTCAAAA AAAAAAAAAA 180
AGAAAGAAAA GAGAAAAGCA TATCACAGCA GAAGACTATA TTCAAACCAT TTATATGAAG 240
CTCAAAAATG AAGCAAAGTT AAGAAAAATG TAGGGATGTA TGGGTAGTGA AAGTTAGGTT 300
GGTGGGCTTT CCTGGGTATT TTATGCTTCA TAAATTAACT TTTATGTATG TAGCTTTTAC 360
ATACATTATA TATATGAATT TGCATGTATT CAGTATTATG TAATACATTA AAAACAATGT 420
TCGCAATGCT AAAAATATAT TGTTGAAGAT TCTGTGTGAA AGCTATACTG TAGTTGTGGC 480
TTTTTATAAC CCTTTCAAGC CCTCTGGGCA GTAGCAGTCC ACCCCTTATT GCCCTCAGTG 540
GACTTCACCT TCTAGGGACT CAGAATTTTT TTTTTTTTTT TGAGACGGAG CTTCGCTCTT 600
TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TGCAAGCTCC GCCTCCCTGG 660
TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGAG CCTGCCACCA 720
CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT GGCCAGGATG 780
GTCTCGATCT CTTGACTTGT GATCCGTCTC GCCTCGGCCT CCCAAAGTGC TGGGATTACA 840
GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC AGGACAGTAC TGTGTGCTGT 900
GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA AGGGCAGGTC TCTGGGATGC 960
CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC TCCTCAAATG TTTATCAAAC 1020
ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT GTCTCAGGAA CCTGCCCAAA 1080
CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA CCCAAGGTCT GTTGGTGACC 1140
AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG 1200
CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA 1260
AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC CAGGCAGAGC TGTCTCCGCC 1320
CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT AGCCAGTGTG GACTCCAACC 1380
TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA TCCTTACTCC CTCCTCTGAC 1440
AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA GTATGAGATA AAAACGCCTC 1500
ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG 1560
AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC TGGTCCTCTC TGAAATCTTT 1620
GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG CATTTGGTTC AAAGGACCAA 1680
GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG TTTCCTTAGC TGGTTGGACT 1740
AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT AATTTTTATC TTAGATTCTA 1800
TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC TTTAATCTTT AATCTTATTT 1860
TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT AGAGAATGCA TTTTTTTTTT 1920
AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT GTAGTAGATG TAGGGTACTG 1980
GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA CCCCAGCTGG GCATCTGGGC 2040
CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT AACGGGCATT CTGCCATGAA 2100
TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT GGGTGCCTGG CATTCATTCC 2160
TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG CAGACTCCTG CCATGGGCCA 2220
GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG CAGGGTGCCT ACTTCTGTGG 2280
TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA ATTACATGGC AGCGTGTGGG 2340
TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC CGGAAACGAT GTTTAGGCCG 2400
AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG AAGAACGAGT GTGAGGAGGA 2460
GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG GAGTGGGGAG AGATGAGGCC 2520
TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT TGGACTTCAT CTTGTGGATG 2580
GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG GTGGCTGGAT CATGGCTTCA 2640
GAAGGCTCTC CCAGGCAGCT GGATGGTGAA GACCAGGTTG GGGAGGTCAC CAGGAGAATG 2700
CTGCCCTAAT CCAGGCAGAG GTGACGGTAG CCTGGGCCAC TTCATCATTA TCACTGAGGC 2760
CTCTCGTGGC TTCCTCAGAC CAGAACGAAG CCCCCTTCTT CAGTGGCTGT GGGCTCACCA 2820
AGTGTCTTCT CCCTCCTCCA 2840