EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-00013 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr1:1003800-1006380 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3934834chr11005806hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr1:1004737-1004751GTGGGGGCGTGGCC-6.39
KLF16MA0741.1chr1:1004739-1004750GGGGGCGTGGC-6.62
KLF5MA0599.1chr1:1004502-1004512GCCCCGCCCC+6.02
KLF5MA0599.1chr1:1004521-1004531GCCCCGCCCC+6.02
KLF5MA0599.1chr1:1004157-1004167GGGGCGGGGC-6.02
KLF5MA0599.1chr1:1004196-1004206GGGGCGGGGC-6.02
Klf1MA0493.1chr1:1005572-1005583TGGGTGTGGCC-6.62
NRF1MA0506.1chr1:1004721-1004732GCGCCTGCGCG+6.14
RFX1MA0509.2chr1:1004774-1004790CGTCGCCATGGTGACC+6.11
RFX1MA0509.2chr1:1004774-1004790CGTCGCCATGGTGACC-6.12
RFX2MA0600.2chr1:1004774-1004790CGTCGCCATGGTGACC+6.2
RFX2MA0600.2chr1:1004774-1004790CGTCGCCATGGTGACC-6.2
SP1MA0079.4chr1:1004499-1004514CAAGCCCCGCCCCTC+6.34
SP2MA0516.2chr1:1004498-1004515GCAAGCCCCGCCCCTCA+6.23
SP3MA0746.2chr1:1004738-1004751TGGGGGCGTGGCC-6.57
SP4MA0685.1chr1:1004499-1004516CAAGCCCCGCCCCTCAT+6.24
SP8MA0747.1chr1:1004738-1004750TGGGGGCGTGGC-6.11
ZNF263MA0528.1chr1:1003831-1003852CCTTCCTCCTCCTCCTGCTCG-6.88
ZNF263MA0528.1chr1:1003819-1003840CCCTCCCCATTTCCTTCCTCC-6.89
ZNF263MA0528.1chr1:1003825-1003846CCATTTCCTTCCTCCTCCTCC-7.03
ZNF263MA0528.1chr1:1003822-1003843TCCCCATTTCCTTCCTCCTCC-8.3
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_24070chr1:1002554-1005867Colon_Crypt_2
SE_24817chr1:1002490-1006081Colon_Crypt_3
SE_27529chr1:1001798-1011077Esophagus
SE_34539chr1:1002321-1004360HCT-116
SE_34539chr1:1004454-1006480HCT-116
SE_41944chr1:1001963-1005965LNCaP
SE_58139chr1:1003761-1004209VACO_9m
SE_58139chr1:1004236-1004768VACO_9m
SE_58139chr1:1004812-1005267VACO_9m
SE_65935chr1:1001682-1006445Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr110052931005547
chr110060441006328
Number: 1             
IDChromosomeStartEnd
GH01I001066chr110018371006486
Enhancer Sequence
CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT 60
CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC 120
CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG 180
CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC 240
GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG 300
GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG 360
GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG 420
AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG 480
GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC 540
ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT 600
GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA 660
GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC 720
AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT 780
GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA 840
GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG 900
GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC 960
GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT 1020
CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG 1080
CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG 1140
GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC 1200
TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC 1260
CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA 1320
GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC 1380
GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG 1440
GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT 1500
GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG 1560
TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG 1620
GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG 1680
TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC 1740
TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG 1800
CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC 1860
AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG 1920
ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG 1980
ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC 2040
TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC 2100
TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT 2160
CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG 2220
GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG GCTCTGAACC 2280
AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC 2340
ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG 2400
TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC CTGTCCCAGT 2460
GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC 2520
CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT TTATTTTAAA AGGTACAATT 2580