EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS078-13849 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr6:6686710-6689290 
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EsrraMA0592.2chr6:6689120-6689131TTCAAGGTCAA+6.14
KLF16MA0741.1chr6:6687267-6687278GCCCCGCCCCC+6.02
KLF5MA0599.1chr6:6687214-6687224GCCCCGCCCC+6.02
KLF5MA0599.1chr6:6687267-6687277GCCCCGCCCC+6.02
NFAT5MA0606.1chr6:6687742-6687752ATTTTCCATT+6.02
NFATC1MA0624.1chr6:6687742-6687752ATTTTCCATT+6.02
NFATC3MA0625.1chr6:6687742-6687752ATTTTCCATT+6.02
ONECUT2MA0756.1chr6:6688823-6688837AAATAATCAATAAA+6.4
ONECUT3MA0757.1chr6:6688823-6688837AAATAATCAATAAA+6.91
SP1MA0079.4chr6:6687336-6687351GAAGCCCCGCCCACT+6.79
SP1MA0079.4chr6:6687409-6687424GAAGCCCCGCCCACT+6.79
SP2MA0516.2chr6:6687335-6687352GGAAGCCCCGCCCACTC+7.16
SP2MA0516.2chr6:6687408-6687425GGAAGCCCCGCCCACTC+7.16
SP4MA0685.1chr6:6687336-6687353GAAGCCCCGCCCACTCC+7.17
SP4MA0685.1chr6:6687409-6687426GAAGCCCCGCCCACTCC+7.17
Sox6MA0515.1chr6:6687891-6687901CCATTGTTTT+6.02
ZNF263MA0528.1chr6:6688034-6688055CCCCCTCTCCCTCCTTCCTTT-6.09
ZNF263MA0528.1chr6:6689239-6689260GGAGAAAGGAGAAAGGGAAGA+6.1
ZNF263MA0528.1chr6:6688033-6688054CCCCCCTCTCCCTCCTTCCTT-6.23
ZNF263MA0528.1chr6:6687222-6687243CCTTCCTGGGCCTCCTCCTCC-6.26
ZNF263MA0528.1chr6:6688030-6688051TTGCCCCCCTCTCCCTCCTTC-6.53
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_00137chr6:6688422-6691846Adipose_Nuclei
SE_09354chr6:6683600-6691412CD14
SE_23153chr6:6686849-6687239Colon_Crypt_1
SE_23153chr6:6687440-6688256Colon_Crypt_1
SE_23153chr6:6688486-6689175Colon_Crypt_1
SE_23777chr6:6686868-6687273Colon_Crypt_2
SE_23777chr6:6687443-6688192Colon_Crypt_2
SE_23777chr6:6688580-6688868Colon_Crypt_2
SE_25016chr6:6686522-6688268Colon_Crypt_3
SE_25016chr6:6688466-6689325Colon_Crypt_3
SE_26283chr6:6686087-6691556Duodenum_Smooth_Muscle
SE_26869chr6:6686831-6691114Esophagus
SE_27854chr6:6686469-6688323Fetal_Intestine
SE_28835chr6:6683151-6688228Fetal_Intestine_Large
SE_29666chr6:6685835-6691263Fetal_Muscle
SE_32005chr6:6686469-6688437Gastric
SE_33501chr6:6686421-6690127H2171
SE_34700chr6:6685359-6691754HeLa
SE_42348chr6:6686682-6692616Lung
SE_48756chr6:6686740-6688299Right_Atrium
SE_50192chr6:6686878-6691045Sigmoid_Colon
SE_52541chr6:6686153-6688359Small_Intestine
SE_65078chr6:6686516-6691258NHEK
Number: 1             
IDChromosomeStartEnd
GH06I006683chr666833866691167
Enhancer Sequence
TCCTGACATA TTGGATTAGA GCCCATTCTA ATGCCTTCGT TTTACCTTAA TTATCTTTTT 60
AAAGGCCTCA TCTCCAAATA CAGTCCCAGT CTGAGGTATG AGGAGGTTAG GGCTTCAAAT 120
ATGAATTTTG AGGGACACAT TTCAGATTAT AACAGATACA TACATATGTA TATCCTATAA 180
ATGAAAATGT CAGGACGGAT TTTAGAGATA CAAGTTTTTA CTTAATTATG ATCCCCCAGC 240
GATCTCATCT CCTCTTAGTC TCAATTTTTC TTGTCTAAGA GAGGGTGCTC CTACCCACAT 300
CTTCAGTCCA AATCCCTCTC CTGAAGGTCG GACCCGCATT TGCAGTGACG GTGACTGGAC 360
ATTTTCTCCC AGGTGTTCGT CAACACTTTC AGCCCTACAG GTCTGAAACA AAACTTACCC 420
ACCTCCAGTG AAGCTCGTCC TCCTGGCCTT TCTGCTTCCT TTTTAAAGTC CATCCCCCTC 480
CAGGCCTCCC ATTACCGGCT GGGAGCCCCG CCCCTTCCTG GGCCTCCTCC TCCGGGGCTT 540
TCAGCTCCTG GCTGGGAGCC CCGCCCCCTC CAGTCCGCCT TTCCAGGCTG AGAGCCCCGC 600
CCATTCCAGG CCTCATCTCC TGGCTGGAAG CCCCGCCCAC TCCAGTCCTC ACCCTCCAGG 660
CTGAGAGCCC CGCCCATTCC AGGCCTCATC TCCTGGCTGG AAGCCCCGCC CACTCCAGTC 720
CTCACCCTCC TGGCTGGGAG CCCCGCCCAC TCCAGGCCTC ACCCTCCAGG CTGGAAGACC 780
CGCCCCTCCC GGGCCTCCGG ATCCTGGCTG GGAGCCATCT CTGCCTCCTG CCGCTTCCTG 840
CACTCCTGAT CAGGTCAGTG GCCAGTCACA GACCTCTGAA ATGTCCTTCC TGACTGTTAG 900
CTCCACAGCA TTCCTACAGC TCCCGCCGCA GTTCCGCCCT CCGGAGGGTT CCAACAGCAG 960
CCCAGTGCGC CTCCCCAGCC CCAGGCTCCC TCCACTCCAG TGAGCCTGCA CCTGGCGCTC 1020
CCTGGCACAC ATATTTTCCA TTGCTCTTCA CTGCCAATTA AATGCAAATT TCTCATCGTG 1080
GGGTTCCAAG TTCTCTGTAT TTGGTCCTCT TATCCTGACA GCTCTACCCT CCCCAGAGCA 1140
CTACAATCTG GCCAAGAGCC TCACCAGCCT ATTCCCCCGA ACCATTGTTT TATTTATTTT 1200
AGATTCAGGG GTATTTGTAT GCAGGTTTGT TACATAAGTA TATTGCGTTA TGATAAGGTT 1260
TGTGCTTCTG ATGATGATCC AGTCGCCCAA CATAGTACCG GATAGTTAGG TTTTCTTCCA 1320
TTGCCCCCCT CTCCCTCCTT CCTTTTGGGG TCCCTGGTGT CTGTTATTCC CATGTTTATG 1380
TCCTTATGTA CCCAGTGTTT AGATCCCACT TATAAGTGAG AGCATGTGGC ATTTGGTTTT 1440
CTGTTTCTGC ATTAGTTTGC TTAGAATAAC GACTGCCAGC TGCATCCATG TTGCTGCAAA 1500
GGACATGATT TCCTTGTTTT TTATGACTGC ACAGTATTCC ATGGCCAAAA AAATGTGGTA 1560
TAAAAATATG TACCACATTT TTTTAATCCA GTCCACAGTC GATGGGCACC TGGGTTGATC 1620
ACATGTCTTC ACTATTGTGA ACAGTGCTGC AATGAACATA CGTGTGCAGG TGTCTTTTTG 1680
GTAGGACTAT TTATATTCCT TTGGGTATAT ACCTAGTAAT GGGATTGCTT GGTCTAATAT 1740
TCATTCTATT TTAGATCTTT AAGAAATCTG CAAACTGCTT TCCACAGGGG CTGCATTAAT 1800
TTGCATTCTC ACCAAAGTGT GTAAGTATTC CCTTTCTCCT CAACCTCTCC AGCATCTGTT 1860
ATTTTTTGAC TTTTTCATAA TAGCCATTCT GACTGGTGTG AAATAGTACT TTATTGAAAC 1920
CACTGCTTTA GAAAGTGAAA GTCCTTTTCA GGTTTGTTTT TCATTCACTG GCAGAGGTTG 1980
CTGGCCCAGC AGGGGTTGTG CAAACTCTGT CTTTGTTCCC CTGTATTTGC CTTCCTCTCC 2040
CTTTTTCCTT CCTTTCCCTT TCTCAATACA CACACACACA CACACACAAC ATGTACAGAA 2100
GGGCTCTTAT CTGAAATAAT CAATAAATAT CAAGGACGTG AAGATGTCAT GCAAGGAGCA 2160
AAGGGGGAAA GTAAACATAA GGAAAATGTA CAAAACCTAA TTTTTCACCA TGTAACCAGC 2220
ATGGGCTTTA AAGTCTACAC AAGACAGACT ACCACAAGCC TCTGCCCCTG CAGAAACTGG 2280
ATAAATCCTG GAGAATGACT ATAATCTCCA TGACACAAAT TCTTCCTCAG AAGGAAGGAT 2340
CAAGGCTTCT GAATAAAAGG GCTAGGAAAA GAAATTTTCC TGAGGCTGCC AAAGGCAAGT 2400
AGGATTCTTT TTCAAGGTCA ACAGGCATTA GAAACAGAAG ACATACACAG TATGCCAGAA 2460
AATTACAAGA TTTCCCTCTC CTTGACACCA AAGAGTTAAA TATAGAAATG TGCATGTGGA 2520
CAGTTATTAG GAGAAAGGAG AAAGGGAAGA GAAGGTGGCC CATTTCCTCC CTTGGCCAAA 2580