EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS082-03048 
Organism
Homo sapiens 
Tissue/cell
HCASMC 
Coordinate
chr1:213097240-213099460 
TF binding sites/motifs
Number: 29             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:213099249-213099267GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr1:213099253-213099271GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr1:213099110-213099128GAAAGAAAGGAAGGGAGA+6.23
EWSR1-FLI1MA0149.1chr1:213099114-213099132GAAAGGAAGGGAGAAAGA+6.23
EWSR1-FLI1MA0149.1chr1:213099222-213099240AGGAGGAAGGAAAGAAGG+6.55
EWSR1-FLI1MA0149.1chr1:213099234-213099252AGAAGGAAGGAAGGAGGA+7.16
EWSR1-FLI1MA0149.1chr1:213099245-213099263AGGAGGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr1:213099207-213099225AAAAGGAAGGAAGGAAGG+7.95
EWSR1-FLI1MA0149.1chr1:213099257-213099275GGAAGGAAGGAAGGACGA+8.29
EWSR1-FLI1MA0149.1chr1:213099211-213099229GGAAGGAAGGAAGGAGGA+8.78
EWSR1-FLI1MA0149.1chr1:213099226-213099244GGAAGGAAAGAAGGAAGG+9.17
EWSR1-FLI1MA0149.1chr1:213099230-213099248GGAAAGAAGGAAGGAAGG+9.47
HEY2MA0649.1chr1:213097772-213097782GGCACGTGTC-6.02
IRF1MA0050.2chr1:213099099-213099120AGAAAGAAAGAGAAAGAAAGG-6.59
IRF1MA0050.2chr1:213099139-213099160AGAAAGAAAGAGAAAGAAAGA-6.76
IRF1MA0050.2chr1:213099153-213099174AGAAAGAAAGAGAAAGAAAGA-6.76
IRF1MA0050.2chr1:213099181-213099202AGAGAGAAAGAGAAAGAAAGA-6.86
IRF1MA0050.2chr1:213099191-213099212AGAAAGAAAGAGAAAGAAAAG-6.95
Npas2MA0626.1chr1:213097772-213097782GGCACGTGTC+6.02
ZNF263MA0528.1chr1:213099216-213099237GAAGGAAGGAGGAAGGAAAGA+6.28
ZNF263MA0528.1chr1:213099212-213099233GAAGGAAGGAAGGAGGAAGGA+6.37
ZNF263MA0528.1chr1:213099235-213099256GAAGGAAGGAAGGAGGAAGGA+6.37
ZNF263MA0528.1chr1:213099239-213099260GAAGGAAGGAGGAAGGAAGGA+6.55
ZNF263MA0528.1chr1:213099208-213099229AAAGGAAGGAAGGAAGGAGGA+6.5
ZNF263MA0528.1chr1:213099250-213099271GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr1:213099223-213099244GGAGGAAGGAAAGAAGGAAGG+7.41
ZNF263MA0528.1chr1:213099246-213099267GGAGGAAGGAAGGAAGGAAGG+7.42
ZNF263MA0528.1chr1:213099243-213099264GAAGGAGGAAGGAAGGAAGGA+7.9
ZNF263MA0528.1chr1:213099220-213099241GAAGGAGGAAGGAAAGAAGGA+8.24
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1213097862213098769
Number: 1             
IDChromosomeStartEnd
GH01I212924chr1213097868213099407
Enhancer Sequence
AGCATGGGGA TTTTTAGCAG CTCCCAGGTG ATGCTAATGT GCGGCCAAGC TTTAGAAGAA 60
GGGATGTCTT TCAGTCCCCT CCTTTTATGG ACCCAACTTC AGAGAGGGGA GGGGCATGCC 120
CAGGATTCTC CATGGGTTAT TGACAGGGCT GACCCCAAAT CCAGTGAGTG CTGCTCTCTA 180
CCCAAAAGGC ATCTCCATTA TCTGTTCAGA AAATGCATTT TAGGGTCTCC TGGCTCTTTC 240
AGTAGAAAGT TCTTCCTTAA GTCACATCCT TCAAGCTTTT CCTTGATCTG CCCAGAGTAG 300
ATTTAGTTTG AATCCAGCAG AAAGTGCAGC TTCACTGAGG TCCTCCCCTC TGCTCAGTTC 360
TGTCCTCCCT TTAAAATCCT GTGCATAGCT GGGGGCGGTG GCTCAAGCCT GTAATCCCAG 420
CACTTTGGGA GGCCAAGGTG GGTGGATCAT GAGGTCAAGA GACCGAGACC ATCCTGGCCA 480
ACATGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAATTA GCTGGGCGTG GTGGCACGTG 540
TCTGTAGTCC CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CGCTTGAACC CAGGAGGCAG 600
AGGTTGCAGT GAGTCAAGAT CGTGCAACTG CACTCCAGCT TGGTGAGAGA GCGAGACTCC 660
ATCTGAAAAA TAAAATAAAA TCCTGTGCAT TGATGTATTC CGTTTCTTGG AGAAGTCTCC 720
GATGATGCAC CTCCTTGGAT GCCTCCCTCT GCTCTACCTC TTTGTCCCTT GCCACTTTGT 780
TTCTGGCCTT CCTTCCTCCA CCTGGCCTCT AGCCCGTTCA TTCTTCTTTG GGCTAGTCCT 840
CCCCAGATCA TCACTGCCCC ACTGAGCTGC TCCCCAGCAA GACCTGGAAA TAAGTGAATT 900
TTTGACTCCT CATTTTTCAC TCCTTCATCC TTGTGACTTC CCTCCAGCTC TGCAAAGGGA 960
GGGCTGGCCC CAGAGGATCC GGCTCTGTCT CCCTCACAGC TGGCAAACAG CTAACTTGAG 1020
TCATGGCCTT GGAACACAAA TAATCTGTTC TCATTTATTT AAAAAATAAA ACAAACCATC 1080
AGCAGCCAAA ACAACACACT GATAAAGGCT TTGGTGAAAG ATGATCCAGA GTAGATAAAC 1140
TGTTCCTTAA TCAGCAGTGT GGTAAATAAA ACCCCTCTTG GGGAGCCTTG CTGAGGGTAT 1200
TTTGGGCAGC CTGGAGAGTT TTTAACCCTC ATTAGCCCCA ACTAAAAATG GAGCCACTGG 1260
AATTTCTGCA CGCAGCTGTT AAGCAGTGAG TAGGACTTTG AGTGTGTTAT TACAAACACT 1320
CTTACTGATT ATGCCTCCCA ATCCCTCAGG AGCAGAGGAG GAGGCTGTTT TGTGCCTATC 1380
TTCCAGGGCT GAGATCACTG CTGCTCTCAC GGTTTCCTGA CAATTTCTTC ACCTCCCAGC 1440
CATTCCCTTG GGCTGAGTAG AACATCCCCT GCTGCCTTTT AGAACTTTGC CAATCATGGC 1500
TGGGCATGGT GGCTCACGGC TGTACTCCCA GCACTTTGGG AGGCCGAGGC AGGCGGATCA 1560
CCTGAGGTCA GGGGTTCAAG ACCAGTCTGG CCAACATGGT GAAACCCCAT GTCTATTAAA 1620
AATGCAAAAA TCAGCTGGGC GTGGTGGGGG GCACCTGTAA TCTCAGCTAC TTGGAAGGCT 1680
GAGGCAGGAG AATCACCTGA ACCTGGGAGG CGGAGGCTGC AGAGAGCCGA GATCACACCA 1740
GTGCACTCCA GCCTGGGCAG CAGAGTGAGC CTCCATGAAA GAAAGAAAGA AAGGAAATGA 1800
AAGAAAGAAA GAAAGAAAGG AAATGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA 1860
GAAAGAAAGA GAAAGAAAGG AAGGGAGAAA GAGAGAGACA GAAAGAAAGA GAAAGAAAGA 1920
AAGAGAAAGA AAGAGAGAAA GAGAGAGAAA GAGAAAGAAA GAGAAAGAAA AGGAAGGAAG 1980
GAAGGAGGAA GGAAAGAAGG AAGGAAGGAG GAAGGAAGGA AGGAAGGAAG GACGATACTG 2040
AAAGCAGAGA ATGATGGCTG AGGGAAGAGG CAGGAAGAGA AAGGTGTATA GAAAAATAAT 2100
CTAGCCCAGA AAGGACAAAG TGGCCACTGC ACACTGAGAT GTCCCATAGA TGTGTCTTCA 2160
TTGGCTTGTA CACTGTTTTG TGATGGAATT TCTTGCTAAC AGTTGAAAAA CCTAAATACT 2220