EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-04786 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr10:31421220-31424410 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1776631chr1031422577hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB3MA0638.1chr10:31422761-31422775GCGCCACGTCACCC+6.07
EWSR1-FLI1MA0149.1chr10:31421974-31421992ACATCCTCCCTCCCTTCC-6.3
EWSR1-FLI1MA0149.1chr10:31422196-31422214GGAAAGGAGGAAGGGAGG+6.88
EWSR1-FLI1MA0149.1chr10:31421982-31422000CCTCCCTTCCTCCCTCCC-6.88
EWSR1-FLI1MA0149.1chr10:31421978-31421996CCTCCCTCCCTTCCTCCC-6.92
EWSR1-FLI1MA0149.1chr10:31422192-31422210GAAAGGAAAGGAGGAAGG+7.05
EWSR1-FLI1MA0149.1chr10:31422204-31422222GGAAGGGAGGGAGGGAGG+7.08
LMX1BMA0703.2chr10:31423921-31423932AATTTAATTAA+6.32
MEOX2MA0706.1chr10:31422236-31422246AGTAATTAAC+6.02
Nr2f6(var.2)MA0728.1chr10:31424180-31424195AAGTTCAAAAGTTCA+6.19
Nr2f6MA0677.1chr10:31423949-31423963CAGGTCAAAGGTCC+6.05
RARAMA0729.1chr10:31424180-31424198AAGTTCAAAAGTTCATAT+6.18
RxraMA0512.2chr10:31424173-31424187AAGGTTAAAGTTCA+6.18
ZNF263MA0528.1chr10:31421974-31421995ACATCCTCCCTCCCTTCCTCC-6.09
ZNF263MA0528.1chr10:31422888-31422909CCCCTCCTCGCCCCCTCCCCC-6.36
ZNF263MA0528.1chr10:31422202-31422223GAGGAAGGGAGGGAGGGAGGA+6.63
ZNF263MA0528.1chr10:31421981-31422002CCCTCCCTTCCTCCCTCCCCA-6.85
ZNF263MA0528.1chr10:31422210-31422231GAGGGAGGGAGGAAAAGAGGG+7.25
ZNF263MA0528.1chr10:31422201-31422222GGAGGAAGGGAGGGAGGGAGG+7.9
ZNF263MA0528.1chr10:31422198-31422219AAAGGAGGAAGGGAGGGAGGG+8.12
ZNF263MA0528.1chr10:31421977-31421998TCCTCCCTCCCTTCCTCCCTC-8.35
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_25423chr10:31420765-31433717DND41
SE_30759chr10:31421649-31424498Fetal_Muscle
SE_39587chr10:31421494-31430224Jurkat
SE_66545chr10:31421494-31430224Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr103142360031424302
Number: 1             
IDChromosomeStartEnd
GH10I031132chr103142154631427344
Enhancer Sequence
TGCAGATCCC TTGATCCCAG CTCCTTCTAT CTCTCAGAGC CTAGGAGGAG TTACGGAGAA 60
ACGGTGCGGC AAAGTTAACA CTGAGCTTCA TCGATATCCT CCAGCTGCAA ATGTTACTAG 120
ATGCTTCTTC AACAAACTAC CTGCCTGAGG ACAGTGCACA TGAACACATC ATAGGCTCTG 180
TAAAATCCTC TGGCAAAGAA ACCTGTTTGC CCGAGGATCC CTTTTTGAGG AGCATCTACT 240
TGACACTCAT TTGGAAGAAG GCAGTTTCAA AATCACCGAG GTGCAGAATA TCACAAAATA 300
ATAAATTTGA AACCACAGCC CCTTGGTACC AGGCAGTTCC CACTGGTACT CGGAGTGGAG 360
CCGTCACAGC TTGTCCTGGC ATCCCAAACA GAAAATGTAT GTATGGATTT CTCACTAACT 420
TAAGAGGAGT CTGACTATTC ATTGGCTCAA CAAGTATTTA TGGGGCATGA GGAGTCAGGC 480
ACAGTGCTGG CTCACGAAAC TTACAGTCCG GTGGGGAGGG TGAATTTTGC CCGGTTGTAC 540
ATTTGATGAG TATTACAAAA GAGAAGATGA AAGAGCTACA GGATCCTGTA ACTGGAGGAC 600
CTGATCTGGC CCAGGCACCA GGGAAGTGAC ATTTCACCTG AGGCCAGAGG AATAAGTGGG 660
AGGGGAATGG GCTGGGGGTG GGCTATGCAG GGAGACCTAT GTGGGCAAAG GGCCTTTCTC 720
CTGGTAAGTT TCTACTCACC CAGCCTCCAC CTGGACATCC TCCCTCCCTT CCTCCCTCCC 780
CAGGAGCTGG GCTGAGGGCC GCCCTACTGC TATCCATGGC ACTTGTCACC CAGAGCCCTG 840
GTGAACTGTT TGCTTGTATG CAGCACCCCT CACCACATGA AGAGCATCTC AAGGGCTAGG 900
AGTCTCGTTT CTTGTATCCC TGGTCCACCG CCTGATCTCC AGCACACATG AGGTATCCAT 960
CAAAATGTTA GCGAAAGGAA AGGAGGAAGG GAGGGAGGGA GGAAAAGAGG GAACAAAGTA 1020
ATTAACGAAT CCCTAGCTGC AGGCACAGGT TGATTCTCTG CAATGTCTCC TTTTCTGTCA 1080
CAGAGAAAAA GAGCACAGTT AGAGTTCACA GGGACCGCGC CCTGCCACAC ATTAATTTAT 1140
TCTCCAAACA TTTGTGGAAG TTGCTAGAGA CACAGATGCA ACGTGTTTTC AGGGAGCTTA 1200
TGATCTAGCA GTGGAAGCGC AACAGAAGTG CAATTCTTTC ATCCTTTTGC CCACATAAAG 1260
CAGGCAAGGC ACGACGAATT TTGATGTCAA CTGCCCAGGC AGGACTTTGT CCCAGCCCAG 1320
CGACCCTCAC GAGGCCAAGG GCAGAGATGA TAGTTGTAAT ATACTCTTCT GTCCATTTCC 1380
TTGATATTCT CCTCAAGGGG TGGGGGGCGC CTGAAATCCA TCTGCCCCGG GGAGAAGGGC 1440
CTCGTGGGCC AGCGCAGCTT GCTCCTCTGC AGACCCAGAA GCATTTGTGC GTCCCGGGCG 1500
TGGCAGGCCC GGCGCCCACT CCGCCCTCCC GCCCCTCCCC CGCGCCACGT CACCCGGGTC 1560
ACGTGAGTGA CCAGGCTCCT CACCCCAACC CCCCTCCCTA CTCCCGCCAG ACTCAGCTGC 1620
TCTCCCCGGG AGCTGGGGAG CCGGGGGCGG GCAGCCGCGT CTGTCCTGCC CCTCCTCGCC 1680
CCCTCCCCCG CAGCCTGAGG AGGGCGTTAA GCAAGGGGCT TCGGAGAAAT TAGAACCAGC 1740
GTTCTAAATT AAGGGGAGCA GATGTCCTTG TTTTGCTCGC GAGGCCTGGG TGGCCTGCTG 1800
TTCAGACAGA AATCGTTGAG GCGCTGACCT TCCGGGACTG CTGTCAATCT CCGCGTGCAG 1860
ATGGCCAGCC CGGAGCCTCG CCGCTCCCCT GCATTGGAAA TGCGGCAGCC GGGGGTGCCG 1920
GCAGCTTGAG AGAAAAGTCT GCGTGGAGGG GGGGTGGGGG GGATGAGGGG AGGCCCGGGG 1980
AGACAGAGGG CAGGAGAAAA AGGCCGGCCC CGCTCACAAT GGAGCCCCTG TGGCGGCCCC 2040
TCCGAGACAA TGCGGTCCCC CGGGACCCGC GGTGGGTTGC GCCAGGCCAG TCCGCGCTCC 2100
AGCTGCCTCT TCAGAACAAG GCAGTGCAAA TGTGCCCACT TGATTCTAAA TCCTCTTAGG 2160
CGCTGTCCAT GTGAACAAGG AAAGGGGTGG CCCTACGATC CTTTACAATC GGAGGCCTGG 2220
GGAGGCCTGG GAGCCCTGGA GCTCCGGAAA ATGTCTGCAC CACGCATGCA AATGGGTCAT 2280
TTCGCTTGGA GAGAGGCATC TGGCGACATC GGCAGAAAGG CTCTCTGCCC GGTAGACGGT 2340
GAACAAAACC CACAAAACCA GCCAGCCAAC AGCGTGCACT AAACACCCCT CTCTGGCCCT 2400
TCAATGCCAC CCGGAGTCCT GAAACATTTT CAGGTTGTTT CCCCTGGAGA GACGTCCCAT 2460
GAAATGTTCA GAAAAGCCAG CTGAGCTGTG CAAAGTCATT AGTCACCCAG GTATTTACAC 2520
TGTTTTTCCT ATTTCCTTTC TCTTTTGGCC TCTGTGGTCA GTGGTATAAA ATTCCTAGGA 2580
ACTCCCACCT AAACACCAGC TTCCTGTTTA TTCTTGCAGT GGCTTTAATG TTTCGCTGTT 2640
AAAAGCGGTT GACCAAGACA CTGAAACAAT CAGTAGAGGT TCGCAGGTGA ATGGAAAAAA 2700
AAATTTAATT AAAAAATATA TCTACTGCTC AGGTCAAAGG TCCAGGTTCA TTTTTACTGC 2760
TTATGTCAGA ATCGCAAAGG GGAAAAGGTA AAATTAAAAT GTAACTTAAT GCCTAAGATC 2820
TTGGTTCAGT TTCATTTGGC CCCTGTGTCT ACATGAACCT ATAAAATACG ATACACTAAA 2880
GTATGAATGT TTTCATTTCT AGCAGTGGAA GGCCTTTTTT TTTTCAATGT GGCATGACGT 2940
TCTTTTGTTA GAGAAGGTTA AAGTTCAAAA GTTCATATAT TAGCACAATC TGTGTGCTCC 3000
TGCGTGTGCC TTACACCTCG CTATGCCTGT TCCGCCTTAA TTTCCTGCAG CAAAACCTTG 3060
CATTTACAGA GCCATCAGAA TTGCAGCCTC CCTGGCCTGG AAAAGAACCC TCGAAGTCAC 3120
CTCATTCAAC CCTTTTCCAA TACTGAATTC CCTGTATGGC CCCTAGGGAG TGTTAGTGAT 3180
GGGACCCTTT 3190