EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-04475 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:161563920-161565340 
TF binding sites/motifs
Number: 33             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr1:161563968-161563983TGGCCAGGGTGACCT-6.25
EWSR1-FLI1MA0149.1chr1:161564768-161564786CCTTCCTGCCTTCCTTCC-10.35
EWSR1-FLI1MA0149.1chr1:161564727-161564745CCTTCCCTCCCTTCCTCC-6.03
EWSR1-FLI1MA0149.1chr1:161564747-161564765CCCTCCTTCCCTCCCTCT-6.03
EWSR1-FLI1MA0149.1chr1:161564719-161564737AAGTCCTTCCTTCCCTCC-6.13
EWSR1-FLI1MA0149.1chr1:161564780-161564798CCTTCCTTCCCCCTTCCC-6.22
EWSR1-FLI1MA0149.1chr1:161564728-161564746CTTCCCTCCCTTCCTCCC-6.27
EWSR1-FLI1MA0149.1chr1:161564739-161564757TCCTCCCTCCCTCCTTCC-6.3
EWSR1-FLI1MA0149.1chr1:161564776-161564794CCTTCCTTCCTTCCCCCT-6.71
EWSR1-FLI1MA0149.1chr1:161564764-161564782TCTCCCTTCCTGCCTTCC-6.83
EWSR1-FLI1MA0149.1chr1:161564743-161564761CCCTCCCTCCTTCCCTCC-6.84
EWSR1-FLI1MA0149.1chr1:161564732-161564750CCTCCCTTCCTCCCTCCC-6.88
EWSR1-FLI1MA0149.1chr1:161564723-161564741CCTTCCTTCCCTCCCTTC-7.36
EWSR1-FLI1MA0149.1chr1:161564772-161564790CCTGCCTTCCTTCCTTCC-9.99
FOXC1MA0032.2chr1:161565190-161565201ATATTTACTTA-6.14
IRF1MA0050.2chr1:161564852-161564873TGTTACTTTCTCTTTCTGTCT+7.37
Stat6MA0520.1chr1:161564606-161564621GACTTCCTGAGAAAT+7.77
ZNF263MA0528.1chr1:161564779-161564800TCCTTCCTTCCCCCTTCCCTC-6.04
ZNF263MA0528.1chr1:161564792-161564813CTTCCCTCCCTCCCTTTCTCC-6.05
ZNF263MA0528.1chr1:161564764-161564785TCTCCCTTCCTGCCTTCCTTC-6.24
ZNF263MA0528.1chr1:161564747-161564768CCCTCCTTCCCTCCCTCTCTC-6.35
ZNF263MA0528.1chr1:161564768-161564789CCTTCCTGCCTTCCTTCCTTC-6.46
ZNF263MA0528.1chr1:161564799-161564820CCCTCCCTTTCTCCCTCCCTA-6.4
ZNF263MA0528.1chr1:161564723-161564744CCTTCCTTCCCTCCCTTCCTC-6.53
ZNF263MA0528.1chr1:161564724-161564745CTTCCTTCCCTCCCTTCCTCC-6.84
ZNF263MA0528.1chr1:161564739-161564760TCCTCCCTCCCTCCTTCCCTC-6.91
ZNF263MA0528.1chr1:161564795-161564816CCCTCCCTCCCTTTCTCCCTC-7.01
ZNF263MA0528.1chr1:161564783-161564804TCCTTCCCCCTTCCCTCCCTC-7.11
ZNF263MA0528.1chr1:161564787-161564808TCCCCCTTCCCTCCCTCCCTT-7.24
ZNF263MA0528.1chr1:161564743-161564764CCCTCCCTCCTTCCCTCCCTC-7.29
ZNF263MA0528.1chr1:161564731-161564752CCCTCCCTTCCTCCCTCCCTC-7.5
ZNF263MA0528.1chr1:161564727-161564748CCTTCCCTCCCTTCCTCCCTC-7.88
ZNF263MA0528.1chr1:161564735-161564756CCCTTCCTCCCTCCCTCCTTC-8.03
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1161563967161564133
chr1161564568161564673
chr1161564222161564487
Number: 1             
IDChromosomeStartEnd
GH01I161594chr1161564591161565390
Enhancer Sequence
TCAGTCTCCC TGATGGGGTT CAGTCTCCTC ACTGAGGAAA TGAGTGGGTG GCCAGGGTGA 60
CCTCTCAGGC CTTCTAGGTC TGACATTCAG GTGGGAGTGT GTAAAGGAAC TTCCAGGAGG 120
ATGCCAGGTA ACTTCCAGAC TGTAGTTAAA GTCAGAGCAT AAAGGAAACC AGAGCTTTCT 180
CCGGGGGTTT CCATGACAGT AGGAACAGGC AGGAAAAAGG CTGTCAAAGA CCCCACCTCA 240
GATGGCTGGA GTATGATTCA GAGCAGAGCC AACAGATTTA AGAGCTTGAG CAAAATATCA 300
CTTGTTCAGC TGTGCTTGCA GCAAGGTTGC ACGTCCGCTG GCCAGGCCCA GTGGTGATAG 360
GGGCCTGTGT TCACACCAGG GCCAAAACAG ATCTGGAAAA TACAAAGTCC AAGCAACTGG 420
ATTATCCATC TTGTTGTGTG GTTCTGTCTG CACTGGCATA AGCACATTTC ATGAGGCATT 480
TTTGCAGCCA GGCATTGGGG CTGCATAAAT GGTTTCTTAA AAATCCTTTC CCAAAAGGCA 540
AAGCTGGTTT GCTGGAATTG TTGGGGAATG TATTAGAATG GGAATTCAGA ATGTGGTTTG 600
CTGCAGAATT TACAGCATGG CAATAAAGGC TCTCTGTGTT CAGGGGGTGA GAGAAGAGAC 660
TAGATGCATT GTGTCAGATG TCTCCCGACT TCCTGAGAAA TGCCACTTTG CAAATACTGG 720
GGCTGCTTTT CACACTGGCC AAGTCAGTTT ATGACAAAAA CATGAGGCAA TTAGGTGTGT 780
TTTGGACACT AACCAGAGAA AGTCCTTCCT TCCCTCCCTT CCTCCCTCCC TCCTTCCCTC 840
CCTCTCTCCC TTCCTGCCTT CCTTCCTTCC CCCTTCCCTC CCTCCCTTTC TCCCTCCCTA 900
AGCTCCCTCC CTGCCTCTCT TTTTCTCTCT CATGTTACTT TCTCTTTCTG TCTTCCTTTT 960
TAATGCCATG GAGTACTATA TTCTTCAAAG TTCCAACAAA GATGCACTAC ATTTGGACAA 1020
TGTGGAAATG GCCCTCAGCC TTCTCTTCCT GATGTGGTCA GCAAAAATCT GGACTTTACT 1080
TCACTCTGAT GCTGAACACC CTGCTCCACA TCTTCCCCAG TATCTCAGAT CCCCAAGCTG 1140
TCTGGTTTGC TTCTAGGAAA GCTCAGCAAT TCCCTGAAAA GAGTGTGGCC CAAGTGACTG 1200
CTTCCCTCCA CCAGTGTGGC CCGTGGGGAA GGCTGTGGCT GGGTGACCCC AAGGGTGGGT 1260
ACATGAGGCC ATATTTACTT AGCCCTTGGC CTTACAGGAC TGTGTCAAGG GGTCAGTAGT 1320
CCTTGCTTTG AGTCTGGTTA TGGTTTTGCA GCCTCAGCAT CAGCGTGGGC AGGCCCTTTT 1380
CAACAGCAGT GCCCTGGCTA ATCCTTTTCT TTTTCCCCAC 1420