EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS019-00549 
Organism
Homo sapiens 
Tissue/cell
CD20+ 
Coordinate
chr1:44404930-44406660 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11210937chr144405563hg19
TF binding sites/motifs
Number: 35             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:44404947-44404965GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr1:44404955-44404973GGAGGGAGGGGAGGGAGG+6.09
EWSR1-FLI1MA0149.1chr1:44405011-44405029GGAAGGAAGGAAGGGGAA+6.42
EWSR1-FLI1MA0149.1chr1:44404968-44404986GGAGGGAAGGAGGGGAGG+6.59
EWSR1-FLI1MA0149.1chr1:44404938-44404956GGAAGGAGGGGAGGGAGG+7.21
EWSR1-FLI1MA0149.1chr1:44404972-44404990GGAAGGAGGGGAGGGAGG+7.21
EWSR1-FLI1MA0149.1chr1:44405003-44405021GGAGAGAGGGAAGGAAGG+7.21
EWSR1-FLI1MA0149.1chr1:44404964-44404982GGAGGGAGGGAAGGAGGG+7.36
EWSR1-FLI1MA0149.1chr1:44404934-44404952GGAAGGAAGGAGGGGAGG+7.79
EWSR1-FLI1MA0149.1chr1:44405007-44405025AGAGGGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr1:44404930-44404948GGAGGGAAGGAAGGAGGG+8.34
FOSL1MA0477.1chr1:44406145-44406156GGTGACTCATG+6.62
FOXF2MA0030.1chr1:44406430-44406444TTAAGGTAAACAAT+6.73
JUNDMA0491.1chr1:44406145-44406156GGTGACTCATG+6.02
ZNF263MA0528.1chr1:44405343-44405364TCCTCTTCCTCTCTCTGCCTC-6.08
ZNF263MA0528.1chr1:44404936-44404957AAGGAAGGAGGGGAGGGAGGG+6.13
ZNF263MA0528.1chr1:44405016-44405037GAAGGAAGGGGAAAGAGAGAG+6.36
ZNF263MA0528.1chr1:44404932-44404953AGGGAAGGAAGGAGGGGAGGG+6.41
ZNF263MA0528.1chr1:44404970-44404991AGGGAAGGAGGGGAGGGAGGG+6.55
ZNF263MA0528.1chr1:44405000-44405021GAGGGAGAGAGGGAAGGAAGG+6.79
ZNF263MA0528.1chr1:44404978-44404999AGGGGAGGGAGGGAGGGGGAG+6.84
ZNF263MA0528.1chr1:44404965-44404986GAGGGAGGGAAGGAGGGGAGG+6.8
ZNF263MA0528.1chr1:44404969-44404990GAGGGAAGGAGGGGAGGGAGG+7.05
ZNF263MA0528.1chr1:44404982-44405003GAGGGAGGGAGGGGGAGGGAG+7.15
ZNF263MA0528.1chr1:44404956-44404977GAGGGAGGGGAGGGAGGGAAG+7.21
ZNF263MA0528.1chr1:44404986-44405007GAGGGAGGGGGAGGGAGGGAG+7.32
ZNF263MA0528.1chr1:44404948-44404969GAGGGAGGGAGGGAGGGGAGG+7.43
ZNF263MA0528.1chr1:44404944-44404965AGGGGAGGGAGGGAGGGAGGG+7.54
ZNF263MA0528.1chr1:44404996-44405017GAGGGAGGGAGAGAGGGAAGG+7.62
ZNF263MA0528.1chr1:44404935-44404956GAAGGAAGGAGGGGAGGGAGG+7.86
ZNF263MA0528.1chr1:44404961-44404982AGGGGAGGGAGGGAAGGAGGG+7.86
ZNF263MA0528.1chr1:44404992-44405013GGGGGAGGGAGGGAGAGAGGG+7.92
ZNF263MA0528.1chr1:44404952-44404973GAGGGAGGGAGGGGAGGGAGG+8.26
ZNF263MA0528.1chr1:44404939-44404960GAAGGAGGGGAGGGAGGGAGG+8.67
ZNF263MA0528.1chr1:44404973-44404994GAAGGAGGGGAGGGAGGGAGG+8.67
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14440509444405400
Number: 1             
IDChromosomeStartEnd
GH01I043938chr14440389744404946
Enhancer Sequence
GGAGGGAAGG AAGGAGGGGA GGGAGGGAGG GAGGGGAGGG AGGGAAGGAG GGGAGGGAGG 60
GAGGGGGAGG GAGGGAGAGA GGGAAGGAAG GAAGGGGAAA GAGAGAGAGA AAGCAAGAAG 120
CAAGCAAGAA AGAAAAGGTT GTTTTCCCCA AAGGAAACAG GCTGCAGAGC TGTACCTCTG 180
TTTACCACAT AGTAGCTATA ACCTGTCACC AGGTGGCACA TTGTAGCTCC TGGGGCCACA 240
GGTGACTCTG GTCAATACTA AAGCCAAAGG CCATTTAGTC CTTTGAAGTC TCAGAAGCAT 300
TCGATAGTGT CAGTCCTCCT TGAAAACCTG TCTTCCCGTG ACTCTCTTGG TCCAATACTC 360
TCCGGGTTCT CCTTCCACTC CTCCAGAGGC TTGTTCTCAG ACGACTTCTG AGTTCCTCTT 420
CCTCTCTCTG CCTCTCATGT TCCTCAGAGC TCTGATACCG ACTCTCTCTC CTCTTCCCAT 480
TCTACTCTCT CCCTGAGCAG CACTGTCTAC TCCCGTGGTT TCAGTTACCA CCTCCATGCT 540
AACCATGCTC ACATTTTATC TCCAGCCTAG AACATTCACC TGAGCCCCAA GTCTGTAATT 600
CCAATACCTC TATCTGTATA TCCTGGGAGA CATCAAGCTT AACATATCCA TACTGGATGT 660
CTTCCGTTTC CTCCTTCAGA TCTGCTGTCC ACCCTTCTCC AGCCTGCTCT GCTCCTCACA 720
TCAATGAGCT TCCCTGCTGT CCAGCTTCCA GACCCTCCCC AGTGTTCCCT GCTCAGTGAG 780
TGCACCAACC TCATCCAGTG ACACAGCCAG AAACTTGGGC AATCTCCTAG GCTCCTTAAG 840
CTCTGTCATG TCCCTTAAGC ATTGGTCACC AAATCCTTAG ATCCTGCAGA TCCATCCCCT 900
TTCCCTATCC CCAGTGCTAT TCTGCTGAAG CCTTCATAAT TTTTTGGATG GTTTATTCCT 960
CATCCTCCTA CCTGGTCTCA CTGTCTCCAG TCACAACTCC CTCCAACCAT TCTCAGCGCT 1020
GCAGCCAGAT AAGTTGCCTT CTCTTCATAT TAACCGAGCA TGAACTGTCG TGCACTGGGC 1080
TAGTTTCAGG GATTCAGAGA CCAGTGAGAA ACATGTTTTG CCATCAAGGA AACTATACTT 1140
GGAGATGGAA GTAGGGGTAG GGTAGCAAAT AAAAGTAAAA GACATCCTGT TAAATTTGGA 1200
TTTCAGGCCC TGCGTGGTGA CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGTGG 1260
GCGGATCATG AGGTCAAGAG AGTGAGACCA CCCTAGCCAA CATGGTAAAA CCCGGTCTCT 1320
ACTAAAAATA TAAAAATTAG CTGGGCGTGG TGGCACGCAC CTGTAGTCCC AGCTACTTGG 1380
GAGGCTGAGG CAGGAGAATC GCTTGAACCC GGGAGGCAGA GGTTGCAGTG AGCCAAGATT 1440
GTGCCACTGC ACTCTAGCCT GGCGACAAAG TGAGACTCTG TCTCAAAAAA AAAAATGGAT 1500
TTAAGGTAAA CAATAAATAC ACCTTTTTTT TTTTTAGATA GGGTCTTGCT GTGTCCCTCG 1560
GGCTGGAGTG CAGTGGTGTG ATCTCAGTTC ACTGCAACCT CCACCTCCTG GGCTCAAGCG 1620
ATCCTCTCAC CTTAGCCTCC TAACTAGCTA AGACTACAGG TGCATTCTAC CACGACTGGC 1680
TAATTTTTAA ATTTTTTTAA TTTTTATTTT TTTGGTAGAG ATGGGCTCTT 1730