EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-06370 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr11:34674340-34676420 
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:34674686-34674704ACATCCTTCCATCCTTCC-6.93
EWSR1-FLI1MA0149.1chr11:34674690-34674708CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674698-34674716CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674706-34674724CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674714-34674732CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674722-34674740CCTTCCATCCTTCCATCC-7.69
EWSR1-FLI1MA0149.1chr11:34674694-34674712CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674702-34674720CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674710-34674728CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674718-34674736CCATCCTTCCATCCTTCC-7.93
EWSR1-FLI1MA0149.1chr11:34674726-34674744CCATCCTTCCATCCTTCC-7.93
POU2F2MA0507.1chr11:34675662-34675675ATATGCAAATGCT-6.33
ZNF263MA0528.1chr11:34674690-34674711CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674698-34674719CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674706-34674727CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674714-34674735CCTTCCATCCTTCCATCCTTC-6.12
ZNF263MA0528.1chr11:34674722-34674743CCTTCCATCCTTCCATCCTTC-6.12
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_23244chr11:34674252-34676211Colon_Crypt_1
SE_26655chr11:34673708-34677938Esophagus
SE_31738chr11:34673765-34676924Gastric
SE_33847chr11:34673660-34677748HCC1954
SE_34914chr11:34672715-34678354HeLa
SE_35339chr11:34673649-34679228HepG2
SE_41618chr11:34674365-34675073LNCaP
SE_41618chr11:34675235-34676052LNCaP
SE_50680chr11:34674352-34676099Sigmoid_Colon
SE_52951chr11:34673750-34676443Small_Intestine
SE_56256chr11:34671428-34679748u87
SE_57552chr11:34675295-34676229VACO_503
SE_64547chr11:34674107-34677482NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr113467465534674926
chr113467557934675977
chr113467507234676258
Number: 1             
IDChromosomeStartEnd
GH11I034652chr113467380134678102
Enhancer Sequence
GAGGTTTTGT TTGGGTCAAG CCCCTTAAAT GAGATGGGGC TGGGAGCCAA TGTAAATGCT 60
TCTGGAATTG AGATTAAGAG CTGAGGCCAG CATAGCTCTC GACTTCTCCT TCCCCCAGTG 120
GTCCTTAGCA TTATGTGTCA CTTGAGGTAT TTGTTAAAAT TAGGGAATAG ATCAAACACT 180
GGCAAGGCTT GGCTGTGTAT TTGCTATTCT GGGGGAACTG AGCCAACCGG GGTAAAATTT 240
CTGTGGCAAT CATTGCCACT CAGTCAAGAC CATGGGGTTC AGGGCTGAGG AAACCTCCCA 300
AGTCACACTC TGAGTTCCTC TGCGACTTCC TACAGTGTCA TCTCCCACAT CCTTCCATCC 360
TTCCATCCTT CCATCCTTCC ATCCTTCCAT CCTTCCATCC TTCCACTTGG GTCTTTGACT 420
TACGGCAAAA AATTCCAACT AAGAATAAAG CTGAACCAAC CACTTCCTGA GCCTCAGGGG 480
CTAGTAGGTC TTGAGGCACC CGGGAAACAA AAACATCATA GTTACAGCTC TGCTGCCCTG 540
ACAGCTGGGC CATCCTCTTT TCTACATCTT GACTTACACC TTCTAGAATC TCAAAATCAA 600
TAGGGGCCTT AGAGGCCAGT TTCTGCTTTT GCATTTGCAG TAGCAAGGAA CTCGCTCTCT 660
CCTGAGTCCA CCGATTGTAT TTTTCAATAG TCCTTCTTAA GATGGGCTCA GGAATCTTCT 720
CTCCTTACCC TTCTGATCCT TGTTTGCTGC AGCTCCCCAT TTCTATCCTG TGATTGTAAC 780
CCAGGCTGGA AAATGAGATC AATCACCCAG GCCCTAAAGA ATCAATGCAG TCTCTGGGGT 840
TGGTGTATTC ATTGGGGTAA TAGCCCTTCA GTAGGATAGT TAATTACAGC CTTATATGGG 900
TCAGTTTCTT TCAGAATAGT TTATAGTCTC TACTGCATGG AAGCAGAACC CCGGAAAAAC 960
CTTGGTCATT TGCCTGAGTC TTTATTTTTC GAGCTCCCAT GTAATTGAAT GCAGTGAAAT 1020
ATCTTTCTAT GTTTTAATGC TAGTTACCAG CTGAGCTAAG GCGAGGCCCA GCGTAAACTG 1080
ATGCCCTCTG TGATAAACGC AGGTGGGGAA ATAGGCTTTG TTTTGATTTC TCTGTCATCT 1140
GCCCATTTCA TAAAATGCCC GCTGCCGGTG TCCTGTTCTG CTCGACAGTC CTCCAGCCTG 1200
TCATGCCAGC TCGGGCTTGA TGTGTTTATC CACTGACTTG TTGAGCCTAA AGCTAGGGTG 1260
GCACGGTCTA TTAGAACACT GAAATTTGTA TATCCCGTAA AGAAATGGCT CACAGCTGAA 1320
TCATATGCAA ATGCTTCTAA TCTTTGCTTC TTGCGAAGCA GCTTAGCTGA AGTCACGCTC 1380
TCTCACTTGC ATCACAAACC TGTGGCTTGT TGCTGCCCCT GCCTGGACTG GATAGGACCT 1440
TGGCCTGGAG TGCCTGGGAG CCAAGCAAGA GAAAGCCAGG CTGGACAACT TCTCCAGGGC 1500
AAGCCATTAT TTTATAAGAA TGAATCACTT AACCACATGG CTAACTTCAA AGGTCTTGAC 1560
TTTTATCCTA GGGCAGAAGA AGGACACATA TTAAAGAGAG GTTAAAGATC AAAAGATATC 1620
AGTGGTAAAG CAGGCCAGTG ATTCCACGGC TTACCCCTGC ACACTGCAAC AGGCAGAGAG 1680
GTCTGGAAGA AATTAGGTTC TTCTTTTGCC TTTGACTGCT TATTCCCCTT TATGATGATG 1740
GAAAGATTTT TATTTGGGGA TTAAAAAAAG AACGTTCCTA GCTGGGTGGA GCCTAGCTTG 1800
GGTAAACGGC TGACAACTCA AAGAATATTT CCTCATGGTT TATCTAGTGT AGAGGTTTTA 1860
GAGTCCATGG ACTGCTGCAT GGGCCACAGC CCCCTGAAAT TGTTGACAAA ATTTCATGTG 1920
TACATATATG TGCATTTTTT TCTGAGGAGA GGGTCCAAGG TTTTCGTCTT ATTCACAAAG 1980
GCACCTGAAC TCTGAAGTAA CTGATTCTAG ATCAACTAGG AACCCACAAA CAATAATTGA 2040
GGCCAATATA CTGAGAGACT CTTGTATTTT TCTGAATTCA 2080