EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS042-18874 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr17:17571100-17574330 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9904468chr1717573187hg19
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr17:17573034-17573052CCCTCCATCCTCCCTTCC-6.98
KLF4MA0039.3chr17:17571495-17571506CCACACCCTGC+6.62
Klf1MA0493.1chr17:17571493-17571504GGCCACACCCT+6.32
PHOX2AMA0713.1chr17:17574155-17574166TAATTAGATTA-6.32
PROP1MA0715.1chr17:17574155-17574166TAATTAGATTA-6.14
Phox2bMA0681.1chr17:17574155-17574166TAATTAGATTA-6.32
RFX2MA0600.2chr17:17572966-17572982TGTTACTATGGTGACC-6.01
RFX2MA0600.2chr17:17572966-17572982TGTTACTATGGTGACC+6.11
RFX5MA0510.2chr17:17572966-17572982TGTTACTATGGTGACC+6.08
RREB1MA0073.1chr17:17572014-17572034CCCCCTCCCACCCCCTCCCG+6.5
SNAI2MA0745.2chr17:17573719-17573729AACAGGTGCA+6.02
ZEB1MA0103.3chr17:17573322-17573333CCCACCTGCCC+6.14
ZNF263MA0528.1chr17:17573018-17573039ATCCCCACTCCCTCCTCCCTC-6.07
ZNF263MA0528.1chr17:17572575-17572596TCCTCTCTCCCTCCCGCCTCT-6.15
ZNF263MA0528.1chr17:17573087-17573108CCCTTCCCCACTCCCTGCCCC-6.18
ZNF263MA0528.1chr17:17573068-17573089TCCCTCCCCATCCCATCCTCC-6.37
ZNF263MA0528.1chr17:17573015-17573036CCCATCCCCACTCCCTCCTCC-6.82
ZNF263MA0528.1chr17:17573039-17573060CATCCTCCCTTCCCCTCCCCC-6
ZNF263MA0528.1chr17:17573026-17573047TCCCTCCTCCCTCCATCCTCC-7.23
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_23508chr17:17571510-17572016Colon_Crypt_1
SE_23959chr17:17571586-17572057Colon_Crypt_2
SE_23959chr17:17572085-17572609Colon_Crypt_2
SE_24961chr17:17571558-17571998Colon_Crypt_3
SE_24961chr17:17572050-17572902Colon_Crypt_3
SE_33725chr17:17568659-17574731H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr171757207917572678
chr171757353217573683
Number: 4             
IDChromosomeStartEnd
GH17I017668chr171757151117572057
GH17I017669chr171757216117572310
GH17I017671chr171757393517574232
GH17I017670chr171757426117574470
Enhancer Sequence
CCCTCCTTGG TTTTTTCTCC CTTTTGTCTG CTGCCCCCAT CCCACAGGCC CTGGAGGGCA 60
GCAGGAAGGA GAAGGGCAGG GGTTGTGGCA TGGCTGAGTG CACCCTCATT TCTAGGGACT 120
CAGGAGAGCA GAAAGAGCTG AGTGCCCCCC AGGAGCAAGC CAGGAAGGGG CCATTCTTGC 180
CTCCAGCGGT GGCTGGGAGC TGGCCCCATC AGGAATGGGG TAAGGCTCCA ACCAGCAGCC 240
CTGAGACCCC AGCCTGGCCC TCTAGGGCTG CACACAGAGT TGCACACACC CCACCCACGT 300
GTGTGGACAG ATGCACACCC CTCCCTCCTT ACACCTGGGC CTCTAACAAC AGTTAGATGC 360
CACAGAGGGC CTGGGCACGC CATCTGTTGT TCAGGCCACA CCCTGCTCTT GCTCAGGTGG 420
AAAACTCTGG AGTGTCCTGG GCTCCTCTCC TCACCCCACG TCAGAAATTC TTGTCTATTC 480
TACCTTCAAG GTATATTTGG AATTGGAATC TTTTCATTGC CCACAGCCCC ACCCTGGCCA 540
GGGCCCCCTG GATTCCCAGG CCTCCTGCTC CTGCCCTGGC CCCTCTCAGC AGCCAGGGTG 600
CACTGTGAGG ACCTAGGGGA GATCCCAGCT CTCCCTGAAG GACCCCGTCA CTCAGGGTCT 660
GAGCCAGAGG CCCCACTGTA CACTGTGGCC ACCCAAGCTG GTCCTGACCC TCTCTGTCCT 720
TGCCTCCTGC TCTCTGCCCC CATGCATTGC TCTTCAGCCC CACAGGCCTC CCCACTGCTC 780
CCGGCACACT CCTGCCTCAG GACCTTTACA CCTGCTGTCT CCTCTTCCCA GCTCCCCACA 840
CATCTGTCCC CTGCCTCCCT CAGGTCTCTA GAGGCTCTAA GACCACCTTC TCTCACCTAA 900
CTAACAAGCT GCTTCCCCCT CCCACCCCCT CCCGCACCCC CTGGGACACT CATCATCCAT 960
AGCTCCTATA TTTACCTTTC TATTTTGTCT GTCTCTCTCC TGCCCCAGAT ACCCACTAGA 1020
ATGTTGGCTC CATGAGGACA TGGATTTGTG TCTGCTTCAG TCACTGTTGC ACCCCTACCC 1080
AGCCCAGCAT CCGGGGCATT GCAGGCTCTA ACACCTGTGG AGGGAAAGAG TGCAGACAGA 1140
GACAGGCAGG GGCAGGTGAC CTGTACACAC TCAAGGCCTA GCGGGGCACT GGCACAGCTG 1200
CACATGCCCA CACCTGCGCA CACACACGCA CACGCGCGCG CGCACACACA CACACACGGG 1260
CCCTGAGCTG AATGCCCTTG GCTCAGTGGG GCCTTGGACG ACAGTCTGGC CCTGGCTCTT 1320
GGGCAGCTGG AGTCTTTGTC CTCACCCAAG ACTGCCAGCC CACCCCAGCT GTGGCTGCTG 1380
ATGCCCCAGA TGGGCCTGCA CTTCTGAAGA GAAAGGACCA GTTTCCTGCA GCCAAACCTC 1440
CAGTGCAGAC CACAGAGCAG CCACGGCATC TGAGCTCCTC TCTCCCTCCC GCCTCTGCAT 1500
CCCTGACTCA TCCCCCACCC CAGGGAGGCA GCCTAGGCCC AACTGCCCCA CTGAGCAGAA 1560
GGGAAGGCTG AGGCAGGAGG CTGAGCCAGC CAGCTGCCCC CGTTAAAGGA GAAGCAGATA 1620
GACGTGGCTT CCAGCCCAGC CCCTCCCTGG CTCAAGCGGT CACCTCCCAA ACAGTCTGAC 1680
CGCAGTCTGT GGGGGCTCCC TGGGCACCCT TGAGCCATGC GTGTGCAGCC AGTATGCACA 1740
CTCCCGCCAG CCGGCCCCTC CAGCCCAGCT TATCACTGAT GACTTTCCCA ACAGAGATCG 1800
ATAGAAAACC TTTTATCTCC TTCCCCGTGG TGGCTCAGAC TCAGGCCTCA GAGCAGAGCT 1860
GGCTCCTGTT ACTATGGTGA CCCTCAAGGA CCTCACTGAC TCCCTCCCAT TCACCCCCAT 1920
CCCCACTCCC TCCTCCCTCC ATCCTCCCTT CCCCTCCCCC ACTCCCACTC CCTCCCCATC 1980
CCATCCTCCC TTCCCCACTC CCTGCCCCAG CCCCTCTCCT ACTCCCTCCC CACCCCCATC 2040
CCACAGCCTG GGATCAATGC TGGTTCCCTA CAGGGCCTGC ACACCTCCCG GCTGCTCATG 2100
GCTGACAGGG AGGGGCCTGG GGGGCTCCTT GCACCCACCC AAGCCCCATC TGCTCCTGGT 2160
CTCGACCTTG CCAGTCCCCC ACTTTCATGC CAAACTACAG CTCCAGTGCC CGATTGAGGC 2220
CTCCCACCTG CCCACACCGT CCTCAGCATT CTGTAACTGC TCACTTATAT CAATGAGTTG 2280
TTTCCCCCTC CATACAGACA GATGGCACCC CTCCATACAG GGCTGCTGGG AGCTGTGAGC 2340
ATTACATAAG CACAAACCTA TGTTGAGTTT GGCCTGTGGC TGATGCTCAA GATATACTAG 2400
CCATTGTTAA TAAGCCTCAA TTTGTGCATT TATTAAATAG GTATAAAAGG TATTATGGTT 2460
GTAAAGATTA AATGAGAGAC AGACACAAAT AGTTTAGCTC ACGGCCTGGC ACGTTCTAAA 2520
CACTACATCC ATGAAGGGAC ACACAGCCTC CCTTCTTCCT TAGCCTCCTT TCTTCCTTTG 2580
TTCTTTGAAG GTGTTTAGGT ATGGGGAGGA GGTGGGAGGA ACAGGTGCAT CCCCGCCCTC 2640
CATGGAGGCT CCATAGCCTT GGCCTGCAGC ATGCAGGCCA AGGAGAACAA TGCCCCATCA 2700
GGGTCCAAGT AACCTGTGCC CTCTCTCTGC CCACAAAGCT ATATTGGTTG TGCCTCACTT 2760
TGGCGGAGGC CAGATTTTCC TCCCATGTTA CCCTTGCCTT CCTGCCTGGA GGCCGGGGCT 2820
GCTCTCTTCC TTCTGCCTGG AATGCCTTGC CATACGGCCA GCCCCACAAT CAGGGAACCA 2880
TCTTCAAGGG AAGTGCTATG GCACCGAGAT CTGGAGCCAG ACCCCCCGGG TCCACATTGC 2940
AGCTGTGCCA CTGCTACCCT CTGAGGCAGC TGCACAGAGG CCTCCCAGGA CCCCACACCC 3000
TCATCCCCGG AGCCTACCAG TGCTCCCTCA GGTGGCAAAA GGGTCTTTGC AGACGTAATT 3060
AGATTACGGA TCTTAAGATT GTTGCAGGCT ATCTGGATGG GCCCCAAATG TAATCACAAG 3120
TGTCCTTGTA TATAAGAAAG AGGCAGAGGG AGCTTCGACT GAGAGGAGGA GCTACGCCGA 3180
TAGAAGCGGA GGTTGCTGTG ATATGAGGAT GGAAGCAAGG ATTCTCCCCC 3230