EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS062-02527 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr10:134264910-134267290 
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR2MA0472.2chr10:134265987-134265998ACGCCCACGCT+6.02
KLF13MA0657.1chr10:134265829-134265847CCTAGAGGGGCGTGACAC-6.4
KLF16MA0741.1chr10:134266447-134266458GGGGGCGGGGC-6.02
KLF5MA0599.1chr10:134266448-134266458GGGGCGGGGC-6.02
KLF5MA0599.1chr10:134266853-134266863GGGGCGGGGC-6.02
NR2C2MA0504.1chr10:134266256-134266271TGACCCCTCACCTCC-6.06
SP1MA0079.4chr10:134266446-134266461GGGGGGCGGGGCCTG-6.65
SP2MA0516.2chr10:134266445-134266462GGGGGGGCGGGGCCTGG-6.26
SP3MA0746.2chr10:134266446-134266459GGGGGGCGGGGCC-6.11
SP4MA0685.1chr10:134266444-134266461GGGGGGGGCGGGGCCTG-6.76
ZNF740MA0753.2chr10:134266442-134266455TTGGGGGGGGCGG-6.54
ZfxMA0146.2chr10:134266447-134266461GGGGGCGGGGCCTG+6.19
ZfxMA0146.2chr10:134265668-134265682GCCGCCTGGGCCTG+6.38
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_09804chr10:134265818-134267072CD14
SE_12419chr10:134264851-134265464CD3
SE_12419chr10:134265476-134267035CD3
SE_20503chr10:134264308-134267043CD56
SE_23106chr10:134263872-134266728Colon_Crypt_1
SE_23106chr10:134266802-134268443Colon_Crypt_1
SE_23746chr10:134263982-134268555Colon_Crypt_2
SE_24681chr10:134263876-134268448Colon_Crypt_3
SE_27260chr10:134264535-134265597Esophagus
SE_27260chr10:134265747-134266615Esophagus
SE_32166chr10:134263985-134268372Gastric
SE_34405chr10:134264707-134265386HCT-116
SE_34405chr10:134265452-134266786HCT-116
SE_41567chr10:134265740-134266705LNCaP
SE_47867chr10:134265830-134266544Pancreas
SE_50630chr10:134264225-134269374Sigmoid_Colon
SE_52741chr10:134264464-134269096Small_Intestine
SE_53287chr10:134265521-134266906Spleen
SE_57559chr10:134265952-134266648VACO_503
SE_60105chr10:134230766-134267420Ly4
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134265015-134267843Pancreatic_islets
SE_68705chr10:134263966-134265342H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10134266616134267060
chr10134266089134266705
Enhancer Sequence
TCTCTTGCCC TCTCAGAGCT CAGGGTACAT TTTGAGCCCA CCTGGCCTGG AGCACGCAGG 60
GCTGGGAGCT GGCTGGGACC TGGACAGGGC TCAGATGCAA AGGCAGCTTC CCCCAGCACC 120
TTCCAGGCTC TGGCTGTTCC AAACCATGCT CCAGGCTCAG ATGGGCTTGT CCCAAAACAG 180
CTGAGCCATT ACCTTCACTT GACAAGGGCC CCCCAAAACA CAGCATTCCA GGGGAATGGG 240
TGACCACCTC GTGGCCACCC CTTGCCTCCC TGCTGGCCCC ATCCTGGGCA GGGGAGCAGC 300
TCCTGCCTCC AGGAACCTTC TCCCAGGAGA CCATGCGCAA CAGAGGGGCG GCGCCCGGCG 360
GGTCAGCACA GAGGCTTGCC TCACCTGCGG TTGCTGAATG AGTGAGTTAG TGGGTGAGGA 420
CCTGCAGGCA GCCCCTGGCT GACACTTTGG CTGTGGAGGA AGAAATCAGG ATGTTCAGGG 480
CCAGAGGGGA AGGTGGCACG GAAGGCAAGA GGGGAGCATC TCCCTGTGGA AGAGCAGGGT 540
GCTGGGTGGG GCATGCTGGG GTGCCGGGAC CCCTGCGCTG GCTGCCACAG TCTGGCAGGG 600
AGCACGCTGC AGCCGCCTGC AGGAGCTGAG CCCAAGGGGA CAGCCGTCCG TGTGTTGGGG 660
AAAGGGGACA GCGATATGTG TGTTGGGGGT GGCCCCGCAT ACCCTCCAGG TAAAGCCATG 720
CACTGTACCT GGGGCGTGGC CCTTGAGTGG CCACTGGAGC CGCCTGGGCC TGAGGGTGGG 780
GTGGGGAGCC CATGTCAGGG TCCAGCCAAA GGTGCCACAG GGCTCCAGCA CCAGAGGCAC 840
CCAGCATGGC CCTGCCTAGC CCTAGGGCCC TCTGCTGCCC AGGGACCCGA CCCTGCAGTC 900
TCTGGGTGGT CAGCGCTGCC CTAGAGGGGC GTGACACCCT CTGCTGGTCC CATACAGAAG 960
GACACAGCTG CCACCCAGCA TGCAGCTCCC CCAGGCACTG GGTGCCCACG CTGTACCCGG 1020
CAGCTTACAC TGTGCCTTGT CACCCACGCT GCACCTGGGA GCCCGCACTG TGCCTAGACG 1080
CCCACGCTGC GCCTGGGACC TCACACTGCA CGAGGTGCCG GCGCCACTCA GGCAGACCAC 1140
CCTCTCCATG TGCGGCAGGA TCCACCAGGG AGGGGCACCC TGACCCTGAT CTCCCCAGGC 1200
AGCTCTGGAA AGGCCTGTGT CCTGGCTGGG GACCTCTGGG AGGCCATGGA GCTGGGAGGG 1260
AGGGACTGGA GGTCTGAGGG ATCCAAGTAG CCCGTCCTGC TGCACCTGCC AGGCCCCAGT 1320
CAGGCCTGGC CATTAAGGCT GAAGGATGAC CCCTCACCTC CTGCCCCTGG GGGCTGAGCC 1380
CTACCTAGGA ACCTGAGTGT TTCCAGCACC TCAGCCCTGG CAGTCCCGGC TAGGCAGATC 1440
CACCCAGCAC CGTGCAGGAG GCCCCAGGAC TGAGCCCCGC AAGGAACATC TCCCAGTGCC 1500
CACAGCCCAC CTAGGGGCCA GTCCACCAGG GATTGGGGGG GGCGGGGCCT GGGAAGGACA 1560
GGGGAAGAGT GAACCACTAG GCCCTGCGTG GCCACTTCCC AGCAGCCAGA TTTAAGGCCA 1620
GGTTAGGATA AATCTCTTGT GCCTCGGTTT CCCCTTCTGT ACCCCAGGAT CACATTACCC 1680
ACCCCCCAAC ACTGTTCTGC AGAATGTGCA GAAAATTGCA GGTGGTGACG CTTCTGCAAA 1740
CAGCAGAGCC CCGGGCACCT GTCCAAGGCG GCTCCGGAAG GCCCCGCGAG TCCCGTGCGC 1800
GGGGACTTCC CAGGGGCGGG GTCGCGGGGC AGGGCGGGCG CTGGCTCCAC CCCCCGCCGG 1860
CCCCGCAGGA ACCGGAAAGG GGCTGGACGG TGTAGCGGCG CCCCCTGCCG ACACCTCCTA 1920
GCATCGCGTC CCCGCGTGGC CGCGGGGCGG GGCCCGGGGG GTCGTTCCGG AGTGGCCCCT 1980
GCAGGGCTTA CAAACAGACG CGGCGGCTGC GAGAGGGGGA CACGATGACT TCTTTCTAGA 2040
GCAGGGACTT AGAGAACCGA GTCTTTATGC ATGAATGTAC CTGCATAACC ATTTGCTAAA 2100
TAGGGCCCGG AGGAGGCTCA TAGGAGGGTG TAGGGGCAGG AGCCTTCTGG CTTTGAGCCC 2160
CAGGGTTGAA GCTGGAGCTT TCCCAGGTGG AGAAGACACA GCGAAGACCA GGGCGGGACG 2220
GCCCGTGGCA GGTGCCGCAC ACCGCGCCGT GGGCTGAGGG ACAGGTCAGG ACCCCAGGCA 2280
CAGAGGTGGG TGGCCAAGCC CCGGCTCCCT GGCCCCTCTC CGAGGCACCA GGGCGTGGTC 2340
CCGAGTTTGG ACTCAGAAGA GACTGTGCAG AGGCTGTGTT 2380